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ENGINEERING PHYSICS

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Engineering Physics
STUDY MATERIAL

For B.E. I/II Semester


As per Jain University Syllabus (sep 2010)

Department of Physics Sri Bhagawan Mahaveer Jain College of Engineering Jakkasandra Post, Kanakapura Taluk, Ramanagaram Dist. 562 112

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MODULE I
QUANTUM PHYSICS
Black Body Radiation A hot body emits thermal radiations which depend on composition and the temperature of the body. The ability of the body to radiate is closely related to its ability to absorb radiation. A Body which is capable of absorbing almost all the radiations incident on it is called a black body. A perfectly black-body can absorb the entire radiations incident on it. Platinum black and Lamp black can absorb almost all the radiations incident on them. Emissive power of a black body: It is defined as the total energy radiated per second from the unit surface area of a black body maintained at certain temperature. Absorptive power of a black body: It is defined as the ratio of the total energy absorbed by the black body to the amount of radiant energy incident on it in a given time interval. The absorptive power of a perfectly black body is 1. Spectral Distribution of energy in thermal radiation (Black Body radiation spectrum) A good absorber of radiation is also a good emitter. Hence when a black body is heated it emits radiations. In practice a black body can be realized with the emission of Ultraviolet, Visible and infrared wavelengths on heating a body. German physicists Lummer and Pringsheim studied the energy density as a function of wavelength for different temperatures of a black body using a spectrograph and a plot is made. This is called Black Body radiation spectrum.

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The Salient features of black body radiation spectrum are as below 1) The energy density increases with wavelength then takes a maximum value Em for a particular wavelength m and then decrease to a value zero for longer wavelengths. Hence the Energy distribution in the spectrum is not uniform 2) As the Temperature increases the Wavelength (m) corresponding to the maximum emission energy (Em) shifts towards shorter wavelength side. Thus the m is inversely proportional to temperature (T) and is called Weins Displacement Law. Mathematically . Here b is Weins Constant of value 2.898x10-3 mK.

3) The total energy emitted by the black body at a given temperature is given by the area under the curve and is proportional to the fourth power of temperature. This is called Stefans law of radiation. Mathematically E = T4 here is the Stefans constant of value 5.67 x 10-8 Wm2K-4. Explanation of Black Body Radiation Spectrum Classical Theories Weins Distribution Law: In the year 1893 Wein using thermodynamics showed that the energy emitted per unit volume in the wavelength range and +d

Here C1 and C2 are empirical constants. A suitable selection for these constants helps to explain the experimental curve in the shorter wavelength region. The drawback of this law is it fails to explain the curve in the longer wavelength region. Also according to this equation the energy density at high temperatures tends to zero which contradicts experimental observations. Rayleigh-Jeans Law: British Physicists Lord Rayleigh and James Jeans made an attempt to explain the Black Body radiation spectrum Based on the concepts formation of standing electromagnetic waves and the law of equipartition of energy. According to this law the energy density of radiation is given by

Here k is Boltzmann constant with value 1.38 x 10-23 JK-1. This law successfully explains the energy distribution of the black body radiation in the longer wavelength region. According to this law black body is expected to radiate large amount of energy in the shorter wavelength region thus leading to no energy available for emission in the longer wavelength region. Experimental observations show that the most of the emissions of the black body radiation occur in the visible and infrared regions. This discrepancy is called Ultraviolet Catastrophe.

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Quantum theory of radiation Plancks law of radiation: German physicist Max Plank successfully explained the energy distribution in the black body radiation based on the following assumptions 1) The surface of the black body contains oscillators 2) These oscillators absorb or emit energy in terms of integral multiples of discrete packets called quanta or photons. The energy E of photons is proportional to the frequency of the radiation. Mathematically E=nh here h is a constant called Plancks constant and its value is 6.625 x 10-34 Js, and n can take integer values 3) At thermal equilibrium the rate of absorption and emission of radiation are equal. According to Plancks law of radiation the expression for energy density of radiation is given by

Where c is the velocity of light, k is Boltzmann constant and h is Plancks constant. This law explains the distribution of energy in the black body radiation spectrum completely for all wavelengths and at all temperatures. Also this law can be reduced to Weins distribution law in the shorter wavelength region and to Rayleigh-Jeans law in the longer wavelength region. Deduction of Weins law, Rayleigh-Jeans law from Plancks law (i) For shorter wavelengths, If is very large, i.e., is very large is very large

.(1)

Using Plancks equation,

, by substituting equation (1) Where,


(ii) For longer wavelengths, If is very small, i.e., Now expand We have,

and
is small, is very small

as power series

.....

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(Since is very small, higher power terms could be neglected)

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Again using Plancks equation, is reduced to This is known as Rayleigh-Jeans law

Photo-Electric effect The emission of electrons from the surface of certain materials when radiation of suitable frequency is incident on it is called the phenomenon of Photo-Electric effect. The electrons emitted are called photo electrons and the material is said to be photo sensitive. This was discovered in the 1887 by Henrich Hertz.

The experimental observations of photoelectric effect are 1) Photo electrons are emitted instantaneously as soon as the radiation is incident 2) Photo electric emission occurs only if the frequency of the incident radiation is greater than a certain value called Threshold frequency. 3) The kinetic energy acquired by photo electrons is directly proportional to the frequency of the incident radiation and is independent of the intensity. 4) The number of photoelectrons emitted depends on the intensity of the incident radiation and is independent of the frequency. Photoelectric effect signifies the particle nature of radiation. Einsteins explanation of the photo electric effect When metal is illuminated with radiation of suitable frequency, the photons of the radiation interact with electrons in the metal. When a photon interacts with an electron, the electron absorbs it and the photon vanishes. The energy acquired by the electron from the photon is made use in two stages. A part of the energy is used by the electron to free itself

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from the metal since it is bound within metal. Thus some minimum amount of energy is required for the electron just to escape from the metal is called Work Function (). The rest of the energy is carried by the electron as Kinetic Energy (KE). Since the energy of the photon is h the photoelectric effect satisfies the following equation This is called Photoelectric Equation. Here is the frequency of the incident radiation

Here

is the threshold frequency and v is the velocity of electron and m the no

mass. Thus from the photoelectric equation, if the frequency of the radiation < photoelectrons are emitted.

Compton Effect The phenomenon of scattering of X-rays from suitable material and hence increase in its wavelength is called Compton Effect.

When X-rays are incident on certain materials they are scattered and the scattered X-rays contain two components. One component has the same wavelength as the incident X-ray and the other with wavelength greater than the incident X-rays. This is due to the scattering of X-ray photons from the electrons present in the material. Due to the transfer of energy from X-ray photon to electron the wavelength of X-ray increases and the electron recoils. This can be treated as collision between two particles. Thus Compton Effect signifies particle nature of radiation. The change in wavelength which is also called Compton Shift is given by

Here is the wavelength of incident X-rays and is the wavelength of scattered X-ray is the scattering angle and m0 is the rest mass of electron. The quantity Compton Wavelength. is called

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Experimental verification A beam of monochromatic X-rays are allowed to fall on a graphite crystal as shown in the figure. The intensity of the scattered X-rays is measure as a function of wavelength of X-

rays, at different scattering angles. At each angle, two peaks appear corresponding to scattered X-ray photons with two different wavelengths. The wavelength of one peak does not change as the angle is varied. This is called primary or unmodified component. We denote it by . The wavelength of the other peak varies strongly with the angle and hence it is called modified component. Ii is denoted by . This effect is called Compton effect. The change in wavelength is called Compton shift. Dual Nature of Radiation and de Broglies hypothesis The phenomenon like Interference, Diffraction and Polarization are attributed to the wave properties of radiation. The Quantum theory of radiation and experiments like Photoelectric effect and Compton Effect describe the particle nature of radiation. Thus radiation behaves like waves and like particles under different suitable circumstances. Hence radiation exhibits dual nature. In the year 1924 French physicist Louis de Broglie made a daring suggestion If radiant energy could behave like waves in some experiments and particles or photons in others and since nature loves symmetry, then one can expect the particles like protons and electrons to exhibit wave nature under suitable circumstances. This is well known as de Broglies hypothesis. Therefore waves can be even associated with moving material particles called Matter waves and the wavelength associated with matter waves is called de Broglie wavelength. The de Broglie wavelength is given by its velocity. where m is the mass of the particle and v is

Expression for de Broglie wavelength (Wavelength of matter wave) According to the Einsteins photon theory the energy of the photon is given by Here is the frequency of the incident radiation and h is Plancks constant. If m is the mass equivalent of the energy of the photon then

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Since the frequency of the incident radiation could be expressed in terms of wavelength as we get, Here p is the momentum of the photon Therefore, Thus, according to de Broglies hypothesis, for a particle moving with velocity v the above equation can be modified by replacing the momentum of photon with the momentum of the moving particle mv. Therefore the de Broglie wavelength associated with a moving particle is given by

(1)
Here m is the mass of the moving particle. de Broglie wavelength of an electron accelerated with a potential difference of V volt Consider an electron accelerated by a potential difference of V volts. The kinetic energy acquired by the electron is given by

Here m is the mass of the electron and is given by 9.1 x 10-31 kg Substituting the value of v in equation (1) we get

Since the electron acquires kinetic energy from the applied potential difference V The kinetic energy of the electron is also given by E=eV where e is the charge on electron with value 1.6 x 10-19C Hence the expression for the de Broglie wavelength

Substituting the values for the constants h, m and e we get

Davisson-Germers experiment: The De-Broglies hypothesis of possibility of wave nature of material particles under appropriate conditions was first experimentally verified by Davisson and Germer. In order to show that particles can also exhibit wave nature, it needs to be proved that material particles can also produce effects such as interference, diffraction, etc which are characteristic phenomena associated exclusively with waves.

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Davisson and Germer were studying the phenomenon of scattering of electrons from material targets and they observed diffraction of electrons in a crystal of nickel, similar to Xray waves undergoing diffraction in crystals, thus proving the wave behavior of electrons. FIGURE:

The experimental apparatus consists of an electron gun to produce a beam of electrons, a solid nickel crystal used as a target mounted on a rotatable stand and an ionization chamber (detector) C which is connected to a galvanometer to collect and measure the current due to the scattered electrons. The electron gun (G) consists of a filament which upon heating by a low-tension battery emits electrons. These emitted electrons are accelerated by applying a high potential from a high-tension battery and using a series of metallic diaphagrams as slits, a narrow beam of electron is obtained. This narrow beam of electrons is incident normally on the Nickel crystal (N) mounted on a rotatable stand. The electrons incident on the Nickel crystal undergo scattering in all directions inside the crystal, just as X-ray waves are scattered in the phenomenon of X-ray diffraction by crystals. The scattered electrons are collected by the ionization chamber (C) and the current due to these collected electrons is measured by the galvanometer connected to the ionization chamber. The ionization chamber can be rotated along a circular path S to collect the electrons at various scattering angles . In the Davisson-Germer experiment, the accelerating potential was kept constant in G and ionization chamber C collects scattered electrons at various scattering angles . For each scattering angle

, the ionization current as measured by the galvanometer was noted

and the same procedure was repeated by applying different potentials to the electron gun G. Initially by applying a constant potential of 40V, the ionization current was noted as a function of scattering angle and the same was repeated by applying 44,48,54,60 and 68 volts respectively. A polar plot of ionization current and scattering angle

for various applied

potentials is obtained as shown in the figures. In the polar plot, for each data point, the angle of inclination to Y-axis equals the scattering angle and the length of the arrow to the data point gives the ionization current.

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At the acceleration potential of 40V, as seen from figure, the variation is found to be smooth without any maxima or minima. However, at V=44volts a distinct maxima was observed as seen in figure and this maxima became more and more pronounced till 54V. With further increase in applied voltage, this maximum declines and fades away as seen in Fig. The values of applied voltage and the scattering angle at which the ionization current was maximum was found to be V=54volts and

=50 degrees (Fig ).

If electrons were to be behaving only as particles, then from classical theories, it is expected that with increasing applied potential, the ionization current due to scattered electrons would increase and therefore, the nature of polar plot at higher potentials should be similar or a laterally pulled version to that of 40volts curve. But as can be seen from the above plots, such behavior is not observed. To explain the observation of distinct maxima of the ionization current over a certain scattering angle , Davisson & Germer proposed that the incident electron beam is scattered from the nickel crystal as a beam of monochromatic waves associated with electrons (i.e., De-Broglie waves or Electron waves associated with the electron) similar to X-ray waves undergoing diffraction in crystals. According to de Broglies hypothesis for an electron accelerated by potential difference of 54 V the de Broglie wavelength is given by

12.26 V

A =

1.226 10 9 54

= 1.66 10 10 m

According to Braggs law the diffracted waves from a crystal undergo constructive interference only for that angle of incidence

which satisfies the equation

n = 2d sin
In the Davisson-Germer experiment the constructive interference was observed at a glancing angle of given by

= 65 0 and it would occur only for those waves with their wavelength = 2d sin (assuming the order of diffraction n to be equal to one).
= 2 0.91 10 10 Sin(65 0 ) = 1.65 10 10 m
10

We therefore have

In the above evaluation we have taken the value of d = 0.91 10 spacing in a nickel crystal.

m for the lattice

The experimentally determined value is in good agreement with the value calculated according to de Broglies hypothesis. Thus Davisson and Germer experiment not only confirms the wave associated with moving particle it also verifies the de Broglies hypothesis.

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Phase velocity and Group velocity

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Phase velocity (vp) The velocity with which a wave travels is called phase velocity and is also called wave velocity. If a point is marked on the wave representing the phase of the particle then the velocity with which the phase propagates from one point to another is called phase velocity. It is given by Substituting for Therefore and Where is the angular frequency and k is wave number.

. We get

Where E is the energy and p is momentum Where c is the velocity of light and v is the velocity of the article.

From the above expression it is evident that the phase velocity is not only greater than the particle velocity it is also greater than the velocity of light. Hence there is no physical meaning for phase velocity of matter waves. Properties of Matter waves The following are the properties associated with the matter waves 1) Matter waves are associated only with particles in motion 2) They are not electromagnetic in nature 3) Group velocity is associated with matter waves 4) The phase velocity has no physical meaning for matter waves 5) The amplitude of the matter wave at a given point is associated with the probability of finding the particle at that point. 6) The wave length of matter waves is given by Group velocity (vg) Since the velocity of matter waves must be equal to that of the particle velocity and since no physical can be associated with phase velocity the concept of group velocity is introduced.

Matter wave can be considered as a resultant wave due to the superposition of many component waves whose velocities differ slightly. Thus a wave group or wave packet is formed. The velocity with which the wave group travels is called group velocity which is same as particle velocity. It is denoted by vg.

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Expression for Group velocity using the concept of superposition of waves Consider a wave group formed by the superposition of a minimum of two waves which slightly differ in their velocities with amplitudes A traveling in the same direction and are represented mathematically as below .(1) .(2) According to the principle of superposition the resultant wave is given by

We know that

..(3)
But and since very small Therefore equation (3) could be written as

..(4)
Compare the eqn.(4) with eqn.(1) Eqn.(4) represents the resultant wave whose amplitude varies as

Which is a constant but varies as a wave As by definition of group velocity with which the variation in amplitude is transmitted in the resultant wave is the group velocity and is given by, or

Relation between group velocity and phase velocity The phase velocity is given by The group velocity of matter waves is given by

.. (1) The wave number k is given by Differentiate the above equation we get,

. (2)

Substituting eqn.(2) in eqn.(1) we get

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The relation between group velocity and phase velocity is given by

Relation between group velocity and particle velocity Consider a particle of mass m moving with a velocity v. We know that the group velocity is given by

But the angular velocity is given by Differentiating we get The propagation constant is given by Differentiating we get

= (1)
The total energy of the particle is given by E= Kinetic energy + Potential energy

Differentiate the above equation we get

The particle velocity

Hence the group velocity and particle velocity are equal.

Heisenbergs Uncertainty Principle Statement: The simultaneous determination of the exact position and momentum of a moving particle is impossible Explanation: According to this principle if x is the error involved in the measurement of position and p is the error involved in the measurement of momentum during their simultaneous measurement, then the product of the corresponding uncertainties is given by

The product of the errors is of the order of Plancks constant. If one quantity is measured with high accuracy then the simultaneous measurement of the other quantity becomes less accurate. Physical significance: According to Newtonian physics the simultaneous measurement of position and momentum are exact. But the existence of matter waves induces serious problems due to the limit to accuracy associated with the simultaneous measurement. Hence the Exactness in Newtonian physics is replaced by Probability in quantum mechanics.

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-ray microscope

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Consider an imaginary experiment in which an electron is tried to be spotted using a high resolution -ray microscope.

The limit of resolution of the microscope

is given by

Here is the wavelength of the scattered -ray photon, is the semi vertical angle. According to the definition of limit of resolution becomes the uncertainty in the determination of position of the electron. In order to observe the electron, the scattered photon from the electron must enter the microscope anywhere within angle of . The x component of momentum px may lie between momentum of the photon is given by and . Here p is the

. Since the momentum is conserved during the

collision, the uncertainty in the x component of momentum is given by

Thus the product of the uncertainties is of the order of h . More rigorous calculation results in the value

Diffraction by single slit Consider a narrow beam of electrons passes through a single narrow slit and produces a diffraction pattern on the screen as shown in the Fig. The first minimum of the pattern is obtained for n=1, in the equation describing the behavior of diffraction pattern due to a single slit. Hence,

y sin = ........(1)
Where y is the width of the slit and first minimum.

is the angle of diffraction corresponding to

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In producing the diffraction pattern on the screen all the electrons have passed through the slit but we can not say definitely at what place of the slit. Hence the uncertainty in determining the position of the electron is equal to the width y of the slit. From equation (1) we have

y =

sin

..(2)

Initially the electrons are moving along the x-axis and hence they have no component of momentum along y-axis. After diffraction at the slit, they are deviated from their initial path to form the pattern and have a component p sin . As y component of momentum may lie anywhere between p sin and p sin . Uncertainty in y component of momentum is

h p y p sin ( p sin ) 2 p sin 2 sin .. (3)

Hence from equations (5) and (6)

y p y

sin y p y h

2h sin

2h

Thus the product of the uncertainties is of the order of h . More rigorous calculation results in the value

Wave function A wave is constituted by a periodic oscillation of a particular physical quantity. For ex, in case of water waves, the quantity that varies is the height surface, in sound waves it is the pressure variation and in case of electromagnetic waves it is the variation of electric and magnetic fields that constitutes the electromagnetic wave. In case of waves associated with material particles (matter waves) the quantity whose variations make up the matter waves is called the wave function and is denoted by . The value of the wave function ( x, y , z , t ) of a body at the point ( x, y , z ) in space and time t , determines the likelihood of finding the body at the location ( x, y , z ) at that instant of time t

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The wave function for a wave moving along x-axis in complex notation is given by Where -angular frequency, k- wave number or propagation constant,

- Amplitude of the wave


Physical significance of wave function just as itself has no direct physical meaning. It is more difficult The wave function to give a physical interpretation to the amplitude of the wave. The amplitude of the wave function is certainly not like displacement in water wave or the pressure wave nor the waves in stretched string. It is a very different kind of wave. But the quantity, the squared Absolute amplitude gives the probability for finding the particle at given location in space and is referred to as probability density. It is given by Thus, in one dimension the probability of finding a particle in the width dx of length x Similarly, for three dimension, the probability of finding a particle in a given small volume dV of volume V is given by here Here P Probability of finding the particle at given location per unit volume and is called Probability Density. According to Max Borns interpretation The wave function is complex the probability density is given by

Where

* is the complex conjugate of

and the above product results in real number.

Normalization and Normalized wave function Since the particle exists somewhere in volume V then the probability of finding the particle in the given volume V is equal 1.

Thus If we are unable to locate the particle in volume V then the notion can be extended to the whole space with

But, normally, the value of the above integral will not be unity but contains an indefinite constant which can be determined along with sign using above considerations. The process

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is called normalization and the wave function which satisfies the above condition is called normalized wave function. Eigen functions and Eigen values The Schrdinger wave equation is a second order differential equation. Thus solving the Schrodinger wave equation to a particular system we get many expressions for wave function ( ). However, all wave functions are not acceptable. Only those wave functions which satisfy certain conditions are acceptable. Such wave functions are called Eigen functions for the system. The energy values corresponding to the Eigen functions are called Eigen values. The wave functions are acceptable if they satisfy the following conditions 1) 2) must be finite everywhere (not zero everywhere) must be single valued which implies that solution is unique for a given position in

space 3) and its first derivatives with respect to its variables must be continuous everywhere. Schrdinger Wave Equation In quantum mechanics, the basic fundamental governing equation which describes the state of the system is the Schrdinger Equation We can determine the motion of an atomic particle using Schrdinger Equation just as we determine the motion of the classical particle using Newtons law. The solution of the Schrdinger Equation gives the wave function of the particle that carries information about the wave behavior associated with the particle. The Schrdinger Equation can be set up in two different contexts. One, which is general and takes care both position and time variations of the wave function, It is called Time dependent Schrdinger Wave Equation. The other one is applicable only to steady state conditions, in which case the wave function can have variation with position not with time. It is called Time independent Schrdinger Wave Equation. Time dependent Schrdinger Wave Equation Consider a particle of mass m moving with velocity v along +ve X-axis. wave length is given by

The deBroglie

h mv

.................. (1)

The wave equation for one dimensional propagation of waves is given by

2 1 2 = x 2 v 2 t 2

along + ve X axis

Where ' v' is Wave Velocity


Here

= 0 e i ( t kx ) ..................(2)

Where 0 is the amplitude at the point of consideration is angular frequency and k is Wave Number. Differentiating equation (2) with respect to time (t), we get

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= i..............(3) t
Differentiating equation (2) twice with respect to x, we get

2 = k 2 .......... ....( 4 ) 2 x
Using Einstein and deBroglie equations

E 2 p 2 and k = h h

Substitute the above in the equations (3) and (4)

2 = iE t h h or = E ........( 5 ) i2 t (3)
( 4) or 2 4 2 = p 2 2 x2 h

h 2 2 = p 2 .........(6) 4 2 x 2

The total energy of the moving particle is given by

E = K.E + P.E or p2 = (E V) 2m

Multiply above equation throughout by , we get

p2 = E V 2m
Substituting, for

E and p 2 from equations (5) and (6) resp., we get,

h 2 1 2 1 h + V = 2 2 i 2 t 4 2m x h 2 2 ih + V = .......(7) 2 2 2 t 8 m x

or

Q 1 = i 2

Equation (7) is the one-dimensional time-dependent Schrdinger equation.

Time-Independent Schrdinger Wave Equation The wave equation which has variations only with respect to position and describes the steady state is called Time-Independent Schrodinger wave equation. Consider a particle of mass m moving with velocity v along +ve X-axis. wave length is given by The deBroglie

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h mv

.................. (1)

The wave equation for one dimensional propagation of waves is given by

2 1 2 = 2 2 x 2 v t

..................(2)

along + ve X axis

Where ' v' is Wave Velocity


Here

= 0 e i (t kx ) ..................(3)

Where 0 is the amplitude at the point of consideration is angular frequency and k is Wave Number. Differentiating twice with respect to time (t), we get

2 = 2 0 e i (t kx ) t 2

..................(4)

Substituting equation (4) in equation (2)

1 2 = 2 2 = 2 v x

( f )

( 2f )2

Here f is the frequency of the wave and is the wave length

4 2 2 = 2 x 2 2 2 4 2 + 2 = 0 x
4 2 + x 2 h 2 mv
2

Substituting for from equation (1) we get

= 0

2 4 2 2 m 2 v 2 =0 + x 2 h 2 2 2 8 2 m 1 + 2 mv 2 = 0 2 h 2 x

..................(5)
1 mv 2 is given by 2

The kinetic energy of the particle

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1 mv 2 = E V here E is the Total Energy of the particle and V is the Potential Energy 2
Therefore equation (5) becomes

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2 x 2

8 2 m( E V ) h2

=0

Generalizing the equation for three dimensions we get

2 2 2 8 2 m( E V ) + + + =0 x 2 y 2 z 2 h2 2 + 8 2 m( E V ) =0 h2
2

Here

2 2 2 + 2+ 2 x 2 y z

Hence the Time-Independent Schrodinger Wave equation for three dimensions. Applications of Schrdinger wave equation Particle in a one dimensional box or one dimensional potential well of infinite height Consider a particle of mass m bouncing back and forth between the walls of one dimensional potential well. The particle is said to be under bound state. Let the motion of the particle be confined along the X-axis in between two infinitely hard walls at x=0 and x=a. Since the walls are infinitely hard, no energy is lost by the particle during the collision with walls and the total energy remains constant. In between walls i.e. 0 < x < a, the potential energy V=0. Beyond the walls i.e. x 0 and x a, the potential energy V=. Since the particle is unable to penetrate the hard walls it exists only inside the potential well. Hence =0 and the probability of finding the particle outside the potential well is also zero.

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Inside the potential well

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Since the potential inside the well is V=0, the Schrodinger wave equation is given by

2 x 2

8 2 m(E 0) h2

=0

2 x 2

8 2 m E h2

=0

2 x 2

+ k2 = 0

.......... .......(1) Here k 2 =

8 2 m E h2

.......... 2) .(

For the given value of E, k is constant. The general solution for the equation (1) is given by

( x) = A sin kx + B cos kx

...............(3) Where A and B are arbitrary constants.

The values of

these constants can be obtained by applying the boundary conditions I) At x=0 , (x)=0 . Substituting the values in equation (3) we get

0 = Asin0 + B cos0 B = 0 Hence equation3) becomes (x) = Asinkx .......... 4) ( ..(


II) At x=a, (x)=0. Substituting the values in equation (4) we get

0 = Asin ka Since A 0 (Otherwiseno Solution ka = n Where n= 1, 2, 3, ), n k = .......... .........( ) 5 a

Thus the wave function becomes

( x) = A sin

n x a

...............(6)

Also substituting the value of k from eq (5) into eq (2) we get


2

8 m E n = h2 a
values.

n2h2 E= 8ma 2

...............(7)

hence

the

energy

Eigen

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Thus substituting n=1 in the equation (7) we get

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E1 =

h2 8ma 2

is the ground state energy of the particle and is also called zero point

energy. Hence E n = n 2 E1 E2 and E3 are energies of the first and second excited states respectively

and so on. Hence for a particle in the bound state, the energy values are discrete. Normalization of wave function The wave function for a particle in a box is given by equation (6)

( x) = A sin

n x a

The value of the arbitrary constant A can be determined by the process of normalization. Since the particle has to exist somewhere inside the box we have
a a

P( x) dx = ( x) dx = 1 Substituting the wave function from equation (6)


2 0 0

A
0

n x sin 2 dx = 1 a
1 [1 cos 2 ] we have 2

Since

sin 2 =

A2 2 n 1 cos a 2 0
a

x dx = 1 Integrating the equation we get


a

A2 2

a 2 n x x 2n sin a = 1 The second term takes the value zero for both the limits 0

A2 [a 0] = 1 A = 2 2 a

Thus the Eigen function is given by

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n ( x) =

2 n x sin a a

The wave functions and the probability densities for the first three values of n are as shown in fig

Thus for ground state (n=1) The probability of finding the particle at the walls is zero and at the centre (a/2) is maximum. The first excited state has three nodes and the second excited state has four nodes.

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MODULE II
NON LINEAR OPTICS LASERS
Laser is an acronym for Light Amplification by Stimulated Emission of Radiation. Laser is a highly monochromatic coherent beam of light of very high intensity. In 1960 Mainmann built the first LASER using Ruby as active medium. Interaction of Radiation with matter: 1. Stimulated Absorption: 2 2 2 2 1 2 2 2 2

2. Spontaneous Emission: -Spontaneous emission is one in which atom in the excited state emits a photon when it returns to its lower energy state without the influence of any external energy.
2

1 1 1 1

If the two atoms are in the same excited state and returns to some lower energy states two photons of having same energy are emitted. These Two photons may not travel in the same direction. They produce in-coherent beam of light. Spontaneous emission is represented as follows, Atom* = Atom + Photon. 3. Stimulated Emission: -Consider an atom in the excited state E2. If a photon of energy E2 - E1 is made to incident on the atom in the excited state E2. The incident photon forces (stimulates) the atom in the excited state to make transition in to ground state E1 by emitting difference in energy in the form of a photon. This type of emission in which atom in the excited state is forced to emit a photon by the influence of another photon of right energy is called stimulated emission. Stimulated emission can be represented as follows.

When stimulated emission takes place, incident photon and the emitted photon are in phase with each other and travel along the same direction. Therefore they are coherent.

Dept. of Physics, Jain University

E E E E

E E E E E h h h h E E E E h h h h h
notohP

E E E

When an atom in the ground state say E1 absorbs a photon of energy (E2 - E1) it makes transition into exited state E2. This is called Stimulated or Induced absorption. It is represented as follows, Photon + Atom = Atom*.

notohP notohP notohP notohP

Consider an atom in the excited state E2. Excited state of an atom is highly unstable. With in a short interval time, of the order of 10-8 sec,atom returns to one of its lower energy state say E1 and emits difference in energy in the form of photon of energy hv = E2 - E1 spontaneously.

Photon + atom* = Atom + (photon + photon).

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ENGINEERING PHYSICS
Lasing Action (Laser Action) : -

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Let an atom in the excited state is stimulated by a photon of right energy so that atom makes stimulated emission. Two coherent photons are obtained. These two coherent photons if stimulate two atoms in the exited state to make emission then four

coherent photons are produced. These four coherent photons so that stimulates 4 atoms in the excited state, 8 coherent photons are produced and so on. As the process continues number of coherent photons increases. These coherent photons constitute an intense beam of laser. This phenomenon of building up of number of coherent photons so as to get an intense laser beam is called lasing action. Population inversion and optical pumping: In an order to produce laser beam there should be more number of stimulated emissions when compared to spontaneous emission. It is possible only if number of atoms in the exited stats is grater than that is the ground state. When system is in thermal equilibrium, then number of atoms in the higher energy level is always less than the number of atoms in the lower energy level. If by some means number of atoms in the exited slate is made to exceed number of atoms in the ground state then population inversion is said to have established between excited state and ground state. The method of achieving the population inversion is called pumping. If light is used to pump electrons to the higher level then the method is called Optical Pumping. If the electric field is used to pump electrons to the higher level then the method is called Electrical Pumping. Metastable State: - Population inversion can be created with the help of three energy levels as follows.
Excited
3

Radiation less Metastable Laser


2

Ground

Let E1 is the ground state of an atom. Let E2 and E3 are the two excited states. If an atom is excited into the energy state, within a short inter of time of 10-8 sec, atom makes a transition into the energy state E2. Let lifetime of the atom in the energy level E2 is of the order of 10-2 to 10-3 sec. Then atoms stay in the excited state E2 for sufficiently long time without making any spontaneous emission.

As more and mare atoms are excited from the ground state to E1 more and more atoms are transferred from E3 to E2. As a result, within a short interval of time population inversion is established between energy level E2 and E1. The energy level E2 in which atoms remain for unusually longer time is called Metastabte state. When transition from E3 to E2 takes place

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E E E E
1 1 1 1

E E E E

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excited atom looses energy in the form of heat without emitting any radiation. Such transitions are called radiation less transition (Non-radiative transitions). Requisites of a Laser System: The Three requisites of a Laser system are 1) Energy Source or Excitation Source for Pumping action 2) Medium Supporting population inversion called Active Medium 3) The Laser Cavity Appropriate amount of energy is to be supplied for the atoms in order excite them to higher energy levels. If the Input energy is in the form of light energy then pumping is called optical pumping. If it is in the form of electrical energy then pumping is called electrical pumping. Population inversion occurs at certain stage in the Active medium due to the absorption of energy. After this stage the Active medium is capable of Emitting laser light. The Laser Cavity consists of an active medium bound between two mirrors. The Mirrors reflect the light two and fro through the active medium. This also helps to tap certain permissible part of laser energy from the active medium. The Ruby Laser Construction

The ruby is a crystal of Al2O3 (Corundum) with some of the Al3+ ions replaced by Cr3+ ions. The chromium ions give the characteristic colour (red) to the ruby crystal. For the purpose of laser production, the doping concentration of chromium ions is 0.05%. A single crystal of ruby in the form of a cylindrical rod is chosen. The length of the rods can vary from 5 to 20 cm while their diameter can vary from 0.5 to 2cm. The end faces of the rod are made optically flat and parallel to each other. One face of the rod is fully silvered while the other face is partially silvered The ruby crystal is placed along the axis of a helical Xenon flash tube. The xenon flash tube is connected to a high voltage pulse generator. For each single voltage pulse, the Xenon tube gives out flashes of powerful light which last for several milliseconds. Surrounding the flash tube is a cylindrical mirror whose function is to reflect light on to the ruby crystal. During the working of the laser a lot of heat is generated. This heat is dissipated by circulating cold water in thin tubes which surround the crystal. The ruby laser satisfies the four requisites needed for any laser system. The crystal rod along with the mirrored faces functions as the resonant cavity. Optical pumping is achieved using light from xenon flash tube. Chromium ions are the active medium, which support population inversion.

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Working

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Shown here is the energy level diagram of chromium ions.

Light from the flash tube excites the ions from the ground state (4A1) to the two higher energy bands (4F1 and 4 F2). Remember when chromium ions interacts the outermost energy levels split into many levels forming a band.

As there are many levels present in this band, the number of photons available, for exciting the ions, are many. Therefore numerous ions are able to absorb the photons and make transition from the ground state to one of the levels of the band. The atoms in the 4F1 and 4F2 band reside there for a period of 10-8s and then make a transition to the metastable levels 2 and . The energy difference between the energy bands and the metastable levels is not released as electromagnetic energy but is taken up by the vibrating atoms of the lattice and is dissipated as heat. These kind of transitions are non- radiative in nature. 4 Therefore F1 2 4 F1
4

F1 2 F2

Non-radiative transitions

The 2 and levels being metastable, the atoms reside in them for an unusually long period of time. In a short while the number of atoms in the two metastable levels is more than the ground level. Thus population inversion is established. Induced transitions between these metastable levels and the ground state give rise to the needed laser radiation. Transition from 2 to the ground state gives rise to photons of wavelength 692.8nm and the transition from to the ground state gives rise to photons of wavelength 694.3nm. The output of the laser is taken from the partially silvered mirror. In the output the intensity of radiation of wavelength 694.3nm is more than the 692.8nm radiation. One of the probable reasons for this could be that the population of the level is more than the 2 level. That is why more photons of wavelength 694.3nm would be released per second. The second probable reason (although not significant) is that the probability of transition from the to the ground level is more than the probability of a transition from 2 level to the ground level. Why it is not significant is that the two levels have an energy difference of only 0.004eV. This is not too great to cause a significant difference in the probabilities.

Application of ruby laser


It is used in holography As drilling requires pulsed laser, ruby lasers are the most suitable The biggest disadvantage of this laser is that since the output is discontinuous, its use is limited to only special applications. Wherever continuous laser beam is required the helium neon laser is more suitable.

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Helium-Neon Laser (Gaseous state laser): -

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Construction: -It consists of quartz discharge tube of length 1m and diameter 1.5cm fitted with Brewsters windows on either side and filled with the mixture of He and Ne gas in the ratio of 10:1. It is placed between two highly parallel plane mirrors one of which is completely silvered while the other is partially silvered. The ends of the tube have two electrodes which are connected to a high power voltage source. Working: The energy level diagram for He and Ne atoms are as shown in the fig. When discharge is produced in the tube large numbers of electrons are produced. These highly energetic electrons collide with He atoms, which are abundant and excite them to energy levels 21s or 23s of He system. This type of collision is called collision of first kind and represented as follows, e1+He He + e2 Where el and e2 are energies of electrons before and after collision. When the helium atoms collide with the neon atoms in the ground state, because of close
3S 2S 2 S coincidence in the energy values ; 2S , resonant energy transfer takes place from helium to neon atoms. As a result, the neon atoms get excited to 2S and 3S levels, whereas the helium atoms return to the ground state. This is called 2nd kind of collision and can be represented as

He* + Ne

Ne* + He

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Here, the states 3S and 2S are called as virtual metastable states because the energy values of 3S and 2S of Ne are equal to the 21S and 23S metastable state of He. Thus population inversion built up between 2S and 3S levels with the lower energy level 2p which leads the laser transitions. [3S to 2p transition gives laser light of wavelength 6328Ao and 2S and 2p transition giving rise to 11523Ao radiation which is in the Infrared region] Applications of Laser Because of high intensity, high degree of monochromaticity and coherence, lasers find remarkable applications in medicine, communication, defence, photography, material processing etc. Laser Welding In performing the task of welding, laser welding is superior to other welding such as arc welding, gas welding, electron welding, etc.

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Focus the laser beam on to the spot to be welded. Due to the excess of heat generated, only focused portion melts. The heat produced by the beam is so intense that, impurities in the material such as oxides float up on the surface and upon cooling the material becomes homogeneous solid structure and it makes a strong joint.

Advantages:

Laser welding is a contact less process and thus no foreign materials can enter into the welded joint. In this type of welding, no destruction occurs in the shape of work piece and the heat is dissipated immediately ( since the total amount of heat supplied is very small compared to the regular welding) The laser beam can be controlled to a great precision, so that we can focus the laser beam precisely to the welding spot. Even we can weld difficult to reach the locations in the material. Since the heat affected zones are very small, laser welding is ideal at places which are surrounded by heat sensitive components.

Laser Cutting Laser cutting of metals is generally associated by gas blowing. The oxygen gas is passed through the nozzle and the tip of the nozzle is pointed at the spot, where the laser beam is focused. The combustion of the gas burns the metal thus reducing the laser power required for cutting. Also the tinny splinters along with the molten part of the metal will blow away by the oxygen jet. The blowing action increases the depth and also the speed of cutting. The laser, which controls the accuracy of the cutting thus, the cut edges will be high quality. Advantages:

The quality of cutting is very high There will be no thermal damage and chemical change when cutting is done in inert atmosphere. 3-d cutting can also be done very easy.

Drilling: Drilling of holes is achieved by subjecting the material to 10-4 to 10-3S duration pulse. The intense heat generated over a short duration by the pulses evaporates the material locally, thus leaving a hole. Advantages:

Conventional Method The tools wear out while drilling

Laser This problem doesnt exist in laser setup

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Whereas it could be done only to a limited extent It is difficult

Drilling can be oblique angle

achieved

at

any

Very fine holes 0.2 to 0.5mm diameter can be drilled. The holes may be even adjacent to each other Very hard material or brittle materials can be drilled. There is no mechanical stress with a laser beam.

Large force has to apply to drill the hard materials or brittle materials.

Measurement of pollutants in atmosphere: The concentration of pollutants in the atmosphere such as carbon monoxide, sulphur dioxide, nitrous oxide, etc, can be measured using laser the way RADAR system is used. Hence it is called LIDAR i.e Light Detection and Ranging. The laser technique consists of a Laser source, retro reflector, optical detector, signal processing unit and analyzer. Project the pulses of laser beam to the atmosphere, the area where the pollutants are to be measured. The back scattered light by the congestion of matter is detected by the photo detector. The reflected laser beam undergoes attenuation due to the absorption by the pollutants in the atmosphere. Since different gases in atmosphere absorb laser energy at different wavelength, the amount of absorbance by each wavelength indicates the amount of pollutants in the atmosphere. The energy of the attenuated beam received at the detector is integrated and compared with the reference laser energy source. The difference in energy called error signal is analyzed and convert into a readout signal by the computer. The reading indicates the concentration and distribution of pollutants at different section in the atmosphere. But it does not give any information about the nature of the scattered particles. However it can be obtained by Raman back scattering experiment. Raman Back Scattering: Laser light is passed through the sample and the spectrum of the transmitted light is obtained. Since laser is a monochromatic, hence, we expect only one line in the spectrum. But due to Raman scattering, we are observing several lines along with the expected line. The other lines of low intensity lie symmetrically above and below to this line. These additional lines are called side bands and their frequencies result when the oscillating frequencies of the gas molecules are added or subtracted from the incident lights frequency. Since different types of gas molecules will have different oscillating frequencies and produce different side band.

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Thus by observing Raman spectra of the back scattered light in the gas sample, the nature of the scattering particles and their compositions can be measured. HOLOGRAPHY HOLO - COMPLETE GRAPHY RECORDING (WRITING)

Holography was discovered by Dennis Gabor in 1948. Defn: Holography is a technique of capturing pictorial details of 3-d on 2-d recording aid, by using the phenomenon of interference. When an object is illuminated with the light source, the light gets reflected and scattered from the various parts of the object and they carry the information of the object in the form of intensity and phase. ** In Photography only the intensity is recorded and the phase information is lost ** In holography both intensity and phase distribution is recorded simultaneously using interference technique. The holographic picture provides 3-d effects even though the recording is of 2-d. Principle of Hologram construction: The interference pattern, which is formed due to the superposition of reference and object beams, has the ability to produce the transmitted effect of the object beam, without the presence of the object, by diffracting the reference beam. ** The photographic plate on which the interference fringes are recorded is the hologram. The holography consist of two steps process called recording and reconstructions of the image. Recording of the image of an object: There are two methods of recording the image, they are: (1) Wavefront division technique: [Wavefront: It is the locus of points where the particles vibrate in the same phase simultaneously.] -> The given object and a mirror are placed one below the other such that a part of the expanded laser beam is incident on the mirror and remaining part falls on the object. ->The part of light reflected from the mirror (plane Wavefront) called reference beam is incident on the photographic plate. When the light incident on the object, every point on the object scatters the incident light. Hence spherical wave fronts generates from each points on the object. The reflected beam is called object beam which incident on the photographic plate.

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The photosensitive surface responds to the resultant effect of interference between the spherical wavelets of the object beam, and the plane waves of the reference beam. Thus the interference effects are recorded on the plate. The interference pattern consists of concentric circular rings pattern that mark successive regions of constructive and distructive interference. The ring pattern is called Gabor Zone Plate. Every set of spherical wavelets that start from each point on the object generates its own zone plates. Thus recording consists of number of zone plates. Such a developed photographic film is called hologram.

(2) Amplitude division technique: In this method an expanded laser source is incident on a beam splitter. The beam splitter reflects a part of the incident light and remaining part will be transmitted. The beam splitter is oriented such that the reflected light incident on the mirror and transmitted light incident on the object. The mirror in-turn reflects the beam called reference beam, directly on to a photographic plate kept at a suitable position for recording the image of the object. The transmitted light, which is incident on the object, gets scattered. The spherical wave fronts associated with the scattered rays serve as object beam and interfere with the reference beam at the photographic plate and the resultant pattern is recorded in it. The photographic plate after the development becomes the hologram of the object.

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Reconstruction Process:

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It is a second step in holography. For the reconstruction of the image, the same laser beam is directed at the hologram in the same direction as the reference beam was incident on it at the stage of recording. When the light is incident on the hologram, diffraction takes place and secondary waves originates from each constituent zone plate, which interfere constructively in certain directions and generate both a real and a virtual image of the corresponding point of the object on the transmission side of the hologram. A real image will be formed infront of the hologram at the same distance as that of the virtual image behind from the hologram. By seeing through the hologram (like seeing through a window) from the transmission side, it appears as though the original object is lying on the other side of it at the same place. This is virtual image due to regeneration. By switching the direction of view, different set of points which corresponds to constructive interference are observed, which regenerate a different prospective of the object. Therefore, it gives three dimensional effects.

Applications of Holography: 1. Holographic interferometry: Interferometry is This is used to study the small distortions of an object that take place such as due to stress or vibration etc. An object beam from an object and a reference beam are made to superpose on a photographic film forming an interference pattern. After the film is developed, it is put back in the same place and the reference beam is now sent again as before. Also the object now is put under stress, so that it undergoes deformation. The object beam from the deformed object superposes on the diffracted reference beam. The diffracted reference beam, which imitates the object beam, forms an interference pattern with the object beam from the stressed object. This interference pattern gives us the information about the kind and the extent of deformation. This is very useful when the deformation is extremely small and as such cannot be determined by other conventional techniques.

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2. Diffraction grating:

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When two parallel beams superpose on the photographic film, the interference pattern consists of parallel straight fringes. The film when developed appears like a grating. The quality of such a grating is much superior when compared to the conventional grating in the sense that the grating constant in this case is truly a constant . 3. Acoustic grating: In this case two coherent ultrasonic breams, one reference and the other reflected from an object, are made incident on a medium. The resulting interference pattern serves as a grating for laser light, which forms an optical image of the object. This is useful for imaging the human body parts and studying physical changes. 4. Encoding : If the reference beam is sent through a mask, then the interference pattern becomes very unique. If an attempt is made to read the hologram and if the person reading the hologram is not aware of the masking used, then he will not be able to decipher the image of the object. This procedure ensures further secrecy in recording information.

OPTICAL FIBERS
Optical fiber is a device used to transmit light signals through the transparent medium made up of dielectric materials like glass from end to other end over a long distance. Construction:1) The innermost Light guiding region called Core. 2) The middle region-covering core made of material similar to Core is called Cladding. The RI of Cladding is less than that of Core. 3) The outermost protecting layer for Core and Cladding from moisture, crushing and chemical reaction etc., is called Sheath. The Optical Fibers are either made as a single fiber or a flexible bundle or Cables. A Bundle fiber is a number of fibers in single jacket. Principles of Optical fibres:It is based on the principle of Total Internal reflection. Consider a ray of light passing from denser medium to rarer medium. As the angle of incidence increases the

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angle of refraction also increases. For a particular angle of incidence called Critical Angle the refracted ray just grazes the interface (Angle of refraction is 90o). If the angle of incidence is greater than Critical Angle then the ray reflected back to the denser medium. This phenomenon is called Total Internal Reflection. TIR is not just one kind of reflections. It may be noted that, some light energy is always lost during reflections occur at the surface of mirror, polished metallic surface. But in case of TIR, there is no loss of light energy at the reflecting surface. The entire incident energy is returned along the reflected light. Hence, it is called TIR. Because of no loss of energy during reflection, the optical fibers are able to sustain the light signal transmission over long distance inspite of infinite number of reflections that occur within the optical fiber. Propagation of light through fiber Optical fiber as a light guide): The incident light enters the core and strikes the interface of the Core and Cladding at large angles as shown in fig. Since the Cladding has lower RI than Core the light suffers multiple Total Internal Reflections. This is possible since by geometry the angle of incidence at the interface is greater than the Critical angle. Since the Total internal reflection is the reflection at the rarer medium there is no energy loss. Entire energy is transmitted through the fiber. The propagation continues even the fiber is bent but not too sharply. Since the fiber guides light it is called as fiber light guide or fiber waveguide. Numerical Aperture: Consider an optical fiber consisting of inner cylindrical core made of glass of refractive index n1 and is surrounded by another material called cladding of refractive index n2 such that n2 < n1.

Consider a ray of light AO incident on the core at O at an angle o with the fiber axis. Then it refracts along OB at an angle of 1 in the core.

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The refracted ray is incident on the interface between core and cladding at B an angle of incidence (90 - 1). Assuming this angle (90 1) is equal to critical angle, then the ray is refracted at 900 to the normal drawn to the interface. i.e. it grazes along BC. Now, it is clear from the figure that any ray that enters into the core at angle i < o will have refractive angle less than 1 because of which its angle of incidence at the interface (=90 - 1) will become greater than critical angle of incidence and thus undergoes total internal reflection. If the angle of incidence at O is greater than o, then the refracted ray pass through the cladding and it will be lost. If AO is rotated around the fiber axis keeping o as constant, then it forms a conical surface called acceptance cone. One those rays which enter within this acceptance cone will undergo total internal reflection and propagates through the fiber. The angle 0 is called waveguide acceptance angle or acceptance cone half angle and Sin0 is called Numerical Aperture of the fiber. The N.A. represents the amount of light rays that can be transmitted along the optical fiber. Expression for N.A.: Let n0, n1 and n2 be the refractive indices of surrounding medium, core and cladding of the fiber respectively. Apply Snells law to the surface PQ, which separates surrounding medium and core: n0

Sin 0 = n1 Sin 1 Sin 0 =

n1 Sin 1 n0

(1)

Apply the Snells law to surface RS which separates core and cladding:

n1 Sin(90 1) = n2 Sin90 n1 Cos 1 = n2 Cos 1 =


n2 n1 n1 n0
(2)

Rewrite the equation (1) => Sin 0 =

1 cos 2 1

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n = 1 n0

2 n2 1 2 n1

2 n 2 n 2 1

n0

If the surrounding medium is air then n0 = 1, Therefore

Sin 0 = N.A. =

2 n 2 n 2 1

The condition for propagation is the angle of incidence i should be less than acceptance angle 0. i.e. i.e.

i < 0

Sin i < Sin 0

Sin i < N.A. Sin i <


2 n 2 n 2 1

sine of the angle of incidence must be less than numerical aperture.

Fractional RI Change ():It is the Ratio of RI difference between Core and Cladding to the RI of core.

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Relation between N A and : -

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Modes of Propagation Light propagates as an electromagnetic wave through an optical fiber. It is true that all waves, having directions above the critical angle, will be trapped within the fiber due to TIR. But is not true that all such waves propagate along the fiber and only certain ray directions are allowed to propagate. The allowed directions correspond to the modes of the fiber i.e. Mode refers to the number of paths for the light rays to propagate in the fiber. The number of modes that a fiber will support depends on d/ . Where d diameter of the core and

is the wavelength of the wave transmitted.

[Note: As a ray gets repeatedly reflected at the walls of the fiber, phase shift occurs. Consequently, the waves traveling along certain zigzag paths will be in phase and intensified, however, some other paths will be out of phase and hence the signal strength diminishes due to destructive interference. The light ray paths along which the waves are in phase inside the fiber are known as modes.] V- Number: The number of modes supported for propagation in the fiber is determined by a parameter called V-number and is given by

V=

2 n 2 n 2 1

no

d diameter of the core,

- wavelength of

the light, n0 R.I. of the surrounding medium, n1 R.I. of the core, n2 R.I. of the cladding Number of modes

V2 2

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Types of Optical Fiber:

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Optical fibers are classified into 3-types based on their R.I. of core and cladding and number of modes of propagation in the fiber. (1) Step index single mode fiber (2) Step index multi mode fiber (3) Graded Index multi mode fiber. (1) Step Index Single Mode optical fiber:

It consists of a core of uniform refractive index n1 The diameter of the core is about 10 m The core is surrounded by a material of uniform R.I. n2 called cladding such that n2 < n1. The external diameter of the cladding is 60 70 m The variation of R.I.s of core and cladding takes the shape of step as shown in fig. Since the core diameter is very small, therefore, it can guide a single mode as shown in figure.

(2)Step index multi mode fiber

(** Construction is similar to that of a single mode fiber) It consists of a core of uniform refractive index n1 The diameter of the core is about 50 200 m The core is surrounded by a material of uniform R.I. n2 called cladding such that n2 < n1. The external diameter of the cladding is 100 250 m The variation of R.I.s of core and cladding takes the shape of step as shown in fig. Since the core diameter is very large, therefore, it will be able to support propagation of large number of modes. LED or Laser can be used as a source. Applications: It can be used in data links which has lower band width requirements. 40

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ENGINEERING PHYSICS
(3)Graded Index multi mode fiber (GRIN)

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The core material has a special feature that its R.I. value decreases in the radially outward direction from the axis and becomes equal to that of the cladding at the interface. It is obvious from the figer that a ray is continuously bent and travels a periodic path along the axis. The ray entering at different angles follow different paths with the same period. The diameter of the core is about 50 200 m The core is surrounded by a material of uniform R.I. n2 called cladding such that n2 < n1. The external diameter of the cladding is 100 250 m Since the core diameter is very large, therefore, it will be able to support propagation of large number of modes. LED or Laser can be used as a source. Applications: It can be used in

Attenuation (Fiber Loss) The loss of light energy of the optical signal as it propagates through the fiber is called attenuation or fiber loss. The main reasons for the loss of light intensity over the length of the cable is due to (i) absorption (ii) Scattering (iii) Radiation loss

(i) Absorption Losses: In this case, the loss of signal power occurs due to absorption of photons associated with the signal. Photons are absorbed by (a) impurities in the silica glass (b) Intrinsic absorption by the glass material. (a) Absorption by impurities: During the light propagation the electrons of the impurity atoms like copper, chromium, iron etc, present in the fiber glass absorb the photons and get excited to higher energy level. Later these electrons give up the absorbed energy either as heat or light energy. But the emitted light will have different wavelength with respect to the signal. Hence it is loss.

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(b) Intrinsic Absorption: some times even if the fiber material has no impurities, but the material itself may absorb the light energy of the signal. This is called intrinsic absorption. (ii) Scattering Loss: (Rayleigh scattering) Since, the glass is heterogeneous mixture of many oxides like SiO2, P2O5, etc, the compositions of the molecular distribution varies from point to point. In addition to it, glass is a non-crystalline and molecules are distributed randomly. Hence, due to the randomness in the molecular distribution and inhomogeneties in the material, there will be sharp variation in the density (refractive index value) inside the glass over distance and it is very small compared to the wavelength of light. Therefore, when the light travels in the fiber, the photons may be scattered. (This type of scattering occurs when the dimensions of the object are smaller than the wavelength of the light. Raleigh scattering

). Due to

the scattering, photons moves in random direction and fails to undergo total internal reflection and escapes from the fiber through cladding and it becomes loss.

(iii)

Radiation loss: Radiation losses occur due to bending of fiber. There are two types of bends:

(a) Macroscopic bends: When optical fiber is curved extensively such that incident angle of the ray falls below the critical angle, then no total internal reflection occurs.

Hence, some of the light rays escape through the cladding and leads to loss in intensity of light

(b) Microscopic bends: The microscopic bending is occur due to non-uniformities in the manufacturing of the fiber or by non-uniform lateral pressures created during the cabling of the fiber. At these bends some of the radiations leak through the fiber due to the absence of total internal reflection and leads to loss in intensity.

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Attenuation co-efficient ( ):

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The net attenuation can be determined by a factor called attenuation coefficient ( ). When light travels in a material medium, there will always be loss in its intensity with distance traveled. The rate of decrease of intensity of light with distance traveled in the homogeneous medium is proportional to the initial intensity called Lambertss law. i.e. if P is the initial intensity and L is the distance propagated in the medium, then,

dP P ( negative sign indicates that it is a decrement) dL dP = P dL


(1)

Or where

is a constant called attenuation coefficient, or simply as attenuation.

Equation (i) can be rewritten as

dP = - dL P

By integrating on both side

dP = P

dL

(2)

If Pin is the initial intensity with which light is entering into the fiber and Pout be the intensity of light at the end of the fiber then equation (2) becomes,
Pout

Pin

dP = P

dL
0

The unit of attenuation for light in optical fiber is Bel.

Or

=-

P 1 log10 out Bel / unitlength P L in

In optical fiber technology, it is customary to express P is in watt and 1B = 10decibel

in terms of decibel/kilometer.

Therefore,

=-

P 10 log10 out dB / km P L in

Dept. of Physics, Jain University

43

ENGINEERING PHYSICS
Applications of Optical Fiber: A typical point to point communication system is shown in figure.

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The analog information such as voice of telephone user is converted into electrical signals in analog form and is coming out from the transmitter section of telephone. The analog signal is converted into binary electrical signal using coder. The binary data comes out as a stream of electrical pulses from the coder. These electrical pulses are converted into pulses of optical power by modulating the light emitted from an optical source like LED. This unit is called an Optical transmitter. Then optical signals are fed into the optical fiber. Only those modes of light signals, which are funneled into the core within the acceptance angle, are sustained for propagation through the fiber by means of TIR. The optical signals from the other end of the fiber are fed to the phtodetector, where the signals are converted into binary electrical signals. Which are directed to decoder to convert the stream of binary electrical signals into analog signal which will be the same information such as voice received by another telephone user. Note: As the optical signals propagating in the optical fiber are subjected to two types of degradation attenuation and delay distortion. Attenuation is the reduction in the strength of the signal because of loss of optical power due to absorption, scattering of photons and leakage of light due to fiber bends. Delay distortion is the reduction in the quality of signal because of spreading of pulses with time. These effects cause continuous degradation of signal as light propagates and hence it may not possible to retrieve the information from the light signal. Therefore, a repeater is needed in the transmission path. An optical repeater consists of receiver, amplifier and transmitter. ADVANTAGES of Optical Fiber:

Dept. of Physics, Jain University

44

ENGINEERING PHYSICS

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1. Optical fibers can carry very large amounts information. 2. The materials used for making optical fibers are silicon oxide and plastic, both are available at low cost. 3. Because of the greater information carrying capacity by the fibers, the cost, length, channel for the fiber would be lesser than that for the metallic cable. 4. Because of their compactness, and light weight, fibers are much easier to transport. 5. There is a possibility of interference between one communication channel and the other in case of metallic cables. However, the optical fiber are totally protected from interference between different communication signals, since, no light can enter a fiber from its sides. Because of which no cross talk takes place. 6. The radiation from lightning or sparking causes the disturbance in the signals which are transmitting in the metallic cable but cannot do for the fiber cable. 7. The information cannot be tapped from the optical fiber. 8. Since signal is optical, no sparks are generated as it could in case of electrical signal. 9. Because of it superior attenuation characteristics, optical fibers support signal transmission over long distances.

Limitations of Optical fiber communications system: 1. Splicing is skilful task, which if not done precisely, the signal loss will be so much. The optic connectors, which are used to connect (splicing) two fibers are highly expensive.

2. While system modifications or because of accidents, a fiber may suffer line break. To establish the connections, it requires highly skilful and time consuming. Hence, maintenance cost is high.

3. Though fibers could be bent to circles of few centimeters radius, they may break when bent to still smaller curvatures. Also for small curvature bends, the loss becomes considerable.

4. Fibers undergo expansion and contraction with temperature that upset some critical alignments which lead to loss in signal power.

Dept. of Physics, Jain University

45

ENGINEERING PHYSICS

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MODULE III
SOLID STATE PHYSICS Crystal Structure
A Crystal is a solid composed of atoms or other microscopic particles arranged in an orderly repetitive array. The study of Crystal physics aims to interpret the macroscopic properties in terms of properties of the microscopic particles of which the solid is composed. The arrangement of atoms in a Crystal is called Crystal Structure. Lattice points and Space Lattice: Points can be imagined in space about which atoms or molecules are located. Such points are called Lattice Points. The totality of such points is called Space Lattice or Crystal Lattice. A Three-Dimensional space lattice (3-D space lattice) may be defined as a finite array of lattice points in three-dimension such that each and every lattice point has identical surrounding in the array.

(2-D Space Lattice) (Lattice point)

Lattice

+ Basis

Crystal Structure

Basis and Crystal structure: -Every lattice point can be associated with one or unit assembly of atoms or molecules identical in composition called Basis or Pattern. The regular periodic three-dimensional arrangement of Basis is called Crystal Structure. Space lattice is imaginary. Crystal structure is real. Bravais and Non-Bravais lattice: - A Bravais lattice is one in which all lattice points are identical in composition. If the lattice points are not identical then lattice is called Non -Bravais lattice. The set of lattice points s together constitutes a Bravais lattice. Similarly the set of lattice points s together constitutes a Bravais lattice. But set of all lattice points s and s together constitute a Non Bravais lattice. Hence a Non-Bravais lattice could be considered as the superposed pattern of two or more interpenetrating Bravais lattices. Dept. of Physics, Jain University 46

ENGINEERING PHYSICS

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Unit cell and Lattice parameters: - In every crystal some fundamental grouping of particles is repeated. Such fundamental grouping particles is called unit cell. A unit cell is chosen to represent the symmetry of the crystal. Hence the unit cell with maximum symmetry is chosen. They are the basic building blocks of the crystal. When these unit cells are translated in three dimensions that will generate the crystal.

Each crystal lattice is described by type of unit cell. But each unit cell is described three vectors a, b and c when the length of the vectors and the angles (,,) between them are specified. They are nothing but the intercepts of the faces and the interfacial angles. All together they constitute lattice parameters.

Primitive Cell :-Some times reference is made to a primitive cell. Primitive cell may be defined as a geometrical shape which, when repeated indefinitely in three dimensions, will fill all space and it consists of lattice points only at corners. It consists of only one atom per cell. There fore unit cells may be primitive (simple) or Non-primitive.

Dept. of Physics, Jain University

47

ENGINEERING PHYSICS

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Crystal systems and Bravais space lattices:- Based on lattice parameters crystals are classified into seven basic systems. If atoms are placed only at corners seven crystal systems yield seven lattices. But few more lattices could be constructed by placing atoms at face center, body center etc., Bravais showed that there are 14 such lattices exist in nature. Hence the name Bravais space lattices. Each crystal system differs from the other in lattice parameters. 1) Cubic Crystal system (Isometric) a=b=c and = = = 90

(Simple or primitive, Face centered (FCC) and Body centered (BCC)),

2) Tetragonal Crystal system (Simple and Body centered)

a=bc

and = = = 90

3) Orthorhombic Crystal system

abc

and = = = 90

(Simple, Face centered (FCC), Body centered (BCC) and Base centered),

4) Monoclinic Crystal system (Simple and Base centered).

abc

and = = 90

5) Triclinic Crystal system (Simple).

abc

and 90

6) Trigonal Crystal system (Rhombohedral) (Simple).

a=b=c

and = = 90

7) Hexagonal crystal system (Simple).

a = b c and = = 90, =120

Dept. of Physics, Jain University

48

ENGINEERING PHYSICS

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Dept. of Physics, Jain University

49

ENGINEERING PHYSICS Directions and Planes: -

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Directions: -In crystals there exists directions and planes in which contain concentration of atoms. It is necessary to locate these directions and planes for crystal analysis. Arrows in two dimensions show directions. The directions are described by giving the coordinates of the first whole numbered point ((x, y) in two dimension,(x,y,z) in three dimension) through which each of the direction passes. Directions are enclosed within square brackets.

Planes: - The crystal may be regarded as made up of an aggregate of a set of parallel equidistant planes, passing through the lattice points, which are known as lattice planes. These lattice planes can be chosen in different ways in a crystal. The problem in designating these planes was solved by Miller who evolved a method to designate a set of parallel planes in a crystal by three numbers (h k l) called Miller Indeces.

Different lattice planes

Dept. of Physics, Jain University

50

ENGINEERING PHYSICS

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Steps to determine miller Indeces of given set of parallel planes: - Miller indices may be defined as the reciprocals of the intercepts made by the plane on the crystallog4raphic axes when reduced to smallest numbers.

Consider a plane ABC which is one of the planes belonging to the set of parallel planes with miller indices (h k l). Let x, y and z be the intercepts made by the plane along the Three crystallographic axes X, Yand Z respectively.

1)

Determine the coordinates of the intercepts made by the plane along the three crystallographic axes.

2) Express the intercepts as multiples of the unit cell dimensions, or lattice parameters along the axes 3) Determine the reciprocals of these numbers 4) Reduce them into the smallest set of integral numbers and enclose them in simple brackets. (No commas to be placed between indeces)
Eg,

1) The intercepts x=2a, y=2b & z=5c Generally x=pa, y=qb, z=rc. 2) The multiples of lattice parameters are x = a 3) Taking the reciprocals a = x 2 1 , y b = 2 1 , & z c = 5 1 a 2a = 2, b y = 2, & c z =5

4) Reducing the reciprocals to smallest set of integral numbers by taking LCM.

1 1 10 , 10 , 10 1 2 5 5 2 5 2

Miller indices of plane ABC = (h k l) =(5 5 2). Dept. of Physics, Jain University

51

ENGINEERING PHYSICS Note: - a) All parallel equidistant planes have the same Miller indices. b) If the Miller indices have the same ratio, then the planes are parallel. c) If the plane is parallel to any of the axes, then the corresponding Intercept is taken to be . Expression for Interplanar spacing in terms of Miller Indeces:

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Consider a Lattice plane ABC, which is one of the planes belonging to the set of planes with Miller indeces ( h k l ) . Let x, y and z be the intercepts made by the plane along the Three crystallographic axes X, Y and Z respectively.

Let OP be the perpendicular drawn form the origin to the plane. Let |,| and | be the angles made by OP with the crystallographic axes X, Y and Z respectively. Let another consecutive plane parallel to ABC pass through the origin. Let a, b and c be the lattice parameters. OP is called interplanar spacing and is denoted by dhkl.

From right angled triangle OCP

cos

OP OC

8 hkl

x =
8 hkl

= cos | = cos
|

OP OB OP OA

y =
8 hkl

but we know that h= b a x x= a h There fore , k = &l = y ,y= k b c O z &z= z c

cos | =

d
52

Dept. of Physics, Jain University

ENGINEERING PHYSICS

PH14/24

a cos | = k b cos | = h c d d

hkl

hkl

hkl

for the rectangular Cartesian coordinate system we have

(cos |)2 + ( cos |)2 + ( cos |)2 = 1

h2 d2 hkl k2 + d2 l
2 hkl 2 + dhkl

a
2 2

=1 c
2

d2 =
hkl

1 h2
2

k 2 l2 +
2 2

b c 1

d
hkl

= h 2 k 2 l2
2

+
2

+
2

is the expression for Interplanar spacing. For a cubic lattice a=b=c, There fore

a d hkil = h2 + k 2 + l 2

Dept. of Physics, Jain University

53

ENGINEERING PHYSICS Definitions

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1) Coordination number: - It is the number of equidistant nearest neighbors that an atom has in a crystal structure. 2) Nearest neighbor distance: - It is the distance between two nearest neighbors in a crystal structure. 3) Atomic packing factor (APF) or Packing fraction: - It is the fraction of space occupied by atoms in a unit cell. It is defined as the ratio of volume occupied by atoms in unit cell to the volume of the unit cell. If the number of atoms per unit cell are n and if Va is the volume of atoms in the unit cell and V is the volume of the unit cell then,
n V APF =
a

4) Lattice Constant: - In a cubic lattice the distance between atoms remains constant along crystallographic axes and is called Lattice Constant. Simple Cubic Structure:

In simple cubic structure each atom consists of 6 equidistant nearest neighbors. Hence its co-ordination number is 6. Eight unit cells share each atom at the corner. Hence only 1/8th of the volume of the atom lies in each cell. Since the atoms are present only at corners, the No. of atoms per unit cell is given by

n=

1 8

8 = 1 atom

We know that the APF is given by Dept. of Physics, Jain University 54

ENGINEERING PHYSICS
n V APF = V 4R 1 APF = a 3
3 3 a

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In this structure the atoms touch each other along the sides of the cube. There fore a = 2 R, Where R is the radius of each atom.

4R 3 APF = 3(2R)3 4R 3 APF = 3 (8 R 3 ) APF = 0.5235

Hence atoms occupy 52.35% off the volume of the unit cell.

Body Centered Cubic (BCC) Structure:

Each atom has 8 equidistant nearest neighbors. Hence the co-ordination number is 8. Since there are eight atoms at corners and 1 atom at the body center, the no. of Dept. of Physics, Jain University 55

ENGINEERING PHYSICS atoms per unit cell is given by


n =1+ 1 8
8 = 2 atoms

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Also in this structure the atoms touch each other along the body diagonal. There fore
(4R)2 = ( 2 a)2 + a2

Where R is the radius of the atom


16R 2 = 2 a2 + a2 = 3a2
2

a2 =

16R 3

a=

4R 3

Now the APF is given by


n V APF = V 4R 3 1 APF = a
3 a

4R 3 1 APF = 3
3

4R 3

APF =

3 8

APF = 0.6802

Hence atoms occupy 68.02% of the volume of the unit

Dept. of Physics, Jain University

56

ENGINEERING PHYSICS Face Centered Cubic (FCC) Structure:

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In FCC structure in addition to atoms at corners, atoms are present at face centers. Each atom consists of 12 equidistant nearest neighbors. Hence the coordination number is 12.

The number of atoms per unit cell is


n= 1 2 6+ 1 8 8 = 4 atoms

In this structure atoms touch each other along the face diagonal. There fore

(4R)2 = a2 + a2 16R 2 = a2 + a2 = 2a2


2

Where R is the atomic radius.

Dept. of Physics, Jain University

57

ENGINEERING PHYSICS
a2 = 16R 2 a= 4R
= 2 2R

PH14/24

The APF is given by

APF =

nVa V
4R 3

1 APF = a 1 APF =
3

4R 3 3

(2
APF = 6

2R

APF = 0.7405

Hence atoms occupy 74.05% of the volume of the unit cell.

X-Ray Diffraction The wavelength of x-ray is of the order of Angstrom (). Hence optical grating cannot be used to diffract X-rays. But the dimension of atoms is of the order of few angstroms and also atoms are arranged perfectly and regularly in the crystal. Hence crystals provide an excellent facility to diffract x-rays. Braggs X-Ray Diffraction and Braggs Law: Bragg considered crystal in terms of equidistant parallel planes in which there is regularity in arrangement of atoms. These are called as Bragg planes. There are different families of such planes exist in the crystal and are inclined to each other with certain angle. In Braggs Diffraction the crystal is mounted such that an X-ray beam is inclined on to the crystal at an angle . A detector scans through various angles for the diffracted Dept. of Physics, Jain University 58

ENGINEERING PHYSICS

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X-rays. It shows peaks for (maximum current) for those angles at which constructive interference takes place. Braggs law gives the condition for constructive interference.

Derivation of Braggs Law: Consider Monochromatic beam of X-Rays. It is incident on the crystal with glancing angle . Ray AB, which is a part of the incident beam, is scattered by an atom at B along BC. Similarly the ray DE is scattered by an atom in the next plane at E along EF. The two scattered rays undergo constructive interference if path difference between the rays is equal to integral multiple of wavelength.

Construction: -Bp and BQ are the perpendiculars drawn as shown in the fig. The path difference = PE + EQ = n ----------- (1) From Right angled triangle PBE Sin = PE BE Dept. of Physics, Jain University 59

ENGINEERING PHYSICS Where BE = d (Interplanar spacing)=dhkl Therefore PE= BE Sin = d Sin Similarly From Right angled triangle QBE QE = BE Sin = d Sin Substituting in (1) = d Sin +d Sin = n = 2 d Sin = n

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Therefore the condition for constructive interference is integral multiple of Wavelength of X- Rays is 2 d Sin = n Hence Braggs Law.

Since Bragg diffraction satisfies the laws of reflection it is also called Bragg reflection.

Braggs X-ray Spectrometer(Determination of wavelength and Interplanar spacing): It is an instrument devised by Bragg to study the diffraction of X-Rays using a crystal as Grating. It is based on the principle of Bragg Reflection.

Dept. of Physics, Jain University

60

ENGINEERING PHYSICS

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Construction: - Monochromatic X-Ray Beam from an X-Ray tube is collimated by slits s1 and s2 and is incident on the crystal mounted on the turntable at a glancing angle . The crystal can be rotated using the turntable. The reflected X-Ray beam is again collimated by slits s3 and s4 and allowed to pass through ionization chamber fixed on the Mechanical Arm. Due to ionization in the medium current flows through the external circuit, which is recorded by the Quadrant Electro Meter (E). In order to satisfy the laws of reflection the coupling between the turntable and the mechanical arm is so made that, if the turntable is rotated through an angle then mechanical arm rotates through an angle 2. Experiment: Rotating the turntable increases glancing angle. Ionization current is measured as a function of glancing angle. The Ionization current is plotted versus glancing angle. It is as shown below.

The angles corresponding to intensity maximum are noted .

The lowest

angle , corresponding to maximum intensity corresponds to the path difference . 2d sin1=n1=

Similarly for next higher angles 2d sin2=n2=2 2d sin3=n3=3 and so on sin1: sin2:sin3 = 1: 2 : 3 (1).

If equation (1) is satisfied for 1,2, and 3 etc. then the Braggs law is verified. By determining using Braggs Spectrometer and by knowing the Dept. of Physics, Jain University

61

ENGINEERING PHYSICS

PH14/24

Value of Interplanar separation (d), Wavelength () of X-Ray beam can be calculated. By determining using Braggs Spectrometer and by knowing the value of Wavelength () of X-Ray beam, Interplanar separation (d) can be calculated. Crystal structure of Sodium Chloride (NaCl): - NaCl is an ionic compound. Hence both Na and Cl are in ionic state. The molecule is under equilibrium because; the attractive force due to ions is balanced by repulsive force due to electron clouds.

The Bravais lattice of NaCl is FCC with the basis containing one Na ion and one Cl ion. The bond length is 2.813. For each atom there are 6 equidistant nearest neighbors of opposite kind. Hence the co ordination number is 6. There are 12 next nearest neighbors of the same kind. The conventional cell which consists of four molecules of NaCl is as shown in the figure. The coordinates of the ions in the conventional cell is as given below. (taking Na ion as origin)

Dept. of Physics, Jain University

62

ENGINEERING PHYSICS

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This structure could be considered as the superposed pattern of two interpenetrating Bravais lattices each made of one type of ion. Crystal structure of Diamond (Allotropic form of Carbon): - Diamond is an allotropic form of carbon. The Bravais lattice is an FCC similar to ZnS. There are 18 carbon atoms in the unit cell. 8 at corners, 6 at face centers and 4 at intermediate tetrahedral positions. The unit cell is as shown in the fig.

In the unit cell, each carbon atom bonds to four other carbon atoms in the form of a tetrahedron. Since each atom has four equidistant nearest neighbors the coordination number is 4.This structure could be considered as the superposed pattern of two interpenetrating Bravais FCC lattices each made of Carbon with one displaced from the other along 1/4th of the body diagonal. The interatomic distance is 1.54 and the lattice constant 3.56.

Dept. of Physics, Jain University

63

c r ce e d o c r ce e d o ....ciiiirttttcelllleiiiid ffffo c r ce e d o no az ra op de ac s no cer d d e de ppa eh gno a a re am eh n depo eved s nemom e op d en no az ra op de ac s no cer d d e de ppa eh gno a a re am eh n depo eved s nemom e op d en noiiiittttaziiiirallllop dellllllllac siiii noiiiittttceriiiid dlllleiiiiffff deiiiillllppa ehtttt gnolllla llllaiiiirettttam ehtttt niiii depolllleved siiii ttttnemom ellllopiiiid tttten no az ra op de ac s no cer d d e de ppa eh gno a a re am eh n depo eved s nemom e op d en ah os a re am c r ce e d o se uce om ro smo a n se c rap degrahc o nemeca ps d ehT ah os a re am c r ce e d o se uce om ro smo a n se c rap degrahc o nemeca ps d ehT ttttahtttt os llllaiiiirettttam ciiiirttttcelllleiiiid ffffo sellllucellllom ro smotttta niiii sellllciiiittttrap degrahc ffffo ttttnemecallllpsiiiid ehT ah os a re am c r ce e d o se uce om ro smo a n se c rap degrahc o nemeca ps d ehT
. ytit n a u q r ot c e v a si d n a e m u l o v t i n u r e p t n e m o m e l o pi d s a d e r u s a e m si n oi t a zi r al o P - :

sc r ce e d o no az ra oP sc r ce e d o no az ra oP sciiiirttttcelllleiiiid ffffo noiiiittttaziiiiralllloP sc r ce e d o no az ra oP

. d e s o p m o c si l a i r et a m e ht h ci h w f o m o t a e h t f o e r ut c u rt s e h t n o s d n e p e d tI .t n a t s n o c ci rt c el ei d ci t a t s d e ll a c si y ti vi t ti m r e p e vi t al e r e h t , s n oi ti d n o c d l e i f ci t a t s r e d n u ,l ai r e t a m ci p o r t o si n a r o F

yti vi tti m r e p ot yt i vi tti m r e p e t ul o s b a f o o it a r e ht y b n e vi g si yti vitti m r e p e v it a l e r e ht sti n u f o m et s y s I S n I . yti vi tti m r e p e t ul o s b A si er e h W ,

si yti s n e d x u lf ci rt c e l e e ht l ai r et a m ci p o rt o si n e vi g a r o f o sl A .t n at s n o c ci rt c e l e i D r o yt i vitt i m r e p e vit al e r d ell a c

ci rt c el ei d t u o hti w r oti c a p a c e ht f o e c n a ti c a p a c e ht si

n oi g e r e ht n e h w s e s a e r c ni r e s n e d n o c e h t f o e c n at i c a p a c e h t t a h t d e r e v o c si d y a d a r a F

l a i r et a m e h t e zi r al o p ot dl ei f ci rt c el e e ht f o yti li b a e ht f o e s u a c e b r u o i v a h e b e l b a k r a m e r ti bi h x e h ci h w , ct e ni al e c r o p , s s al g s a h c u s sl ai r e t a m g n it c u d n o c - n o n yl l a ci rt c el e e r a

DIELECTRIC PROPERTIES OF SOLIDS

ENGINEERING PHYSICS

MODULE IV

s e vi g

0C

/ C oi t a r e h t n e h t c i r t c el ei d h ti w r o ti c a p a c e h t f o e c n a ti c a p a c e h t si C d n a

n oi t a u q e e h t y b h t g n e r t s dl e i f d ei l p p a e h t o t d e t al e r

0C

fI . ci rt c el e i d hti w d el li f si s et al p e h t n e e wt e b

. s el o pi d ci rt c el e g nit a e r c

na snoC c r ce e D ttttnattttsnoC ciiiirttttcelllleiiiiD na snoC c r ce e D na snoC c r ce e D

sc r ce e D sc r ce e D sciiiirttttcelllleiiiiD sc r ce e D

. e c a p s e e r f f o yti vi tti m r e p si

.t n at s n o c ci rt c el ei d r o yti vi tt i m r e p e vit al e r si

. e c a p s e erf f o

. e m ul o v ti n u r e p s e l u c e l o m f o r e b m u n s i N d n a el u c el o m r e p t n e m o m el o p i d e g a r e v a si

= E

. y ti li b a zi r a l o p d e ll a c y t il a n o i t r o p o r p f o t n a t s n o c a si

Dept. of Physics, Jain University


er e h w o sl A er e h W

r r P=N

PH14/24

64

. s el o p i d l a u di vi d ni f o st n e m o m e l o p i d f o m u s r ot c e v e ht si d n a l ai r et a m e ht ni t n e m o m el o pi d t e n f o t n e m p ol e v e d e ht ot s d a el si h T .l ai r e t a m e h t ni hti w d e c u d ni e r a s el o p i d e c n e H . dl ei f ci rt c el e d e il p p a ot e u d l a i r et a m ci rt c el e i d f o s el u c el o m r o s m ot a ni s e g r a h c e vit a g e n f o r et n e c e vit c e ff e e ht m o rf s e g r a h c e vit i s o p f o s r e t n e c e vit c eff e f o n o it a r a p e s e ht ot e u d si d n a l ai r et a m ci rt c el ei d e h t t u o h g u o r ht s r u c c o si h T - :

P+ P+ P+ P=P P+ P+ P+ P=P P + oP + iP + eP = P P+ P+ P+ P=P

. s m si n a h c e m n oit a zi r a l o p r u o f ll a f o n oit u bi rt n o c e ht ot e u d si l a i r et a m e h t f o n oit a zi r al o p t e n e h T

e r a y e h T . s m si n a h c e m t n e r e ffi d r u o f h g u o r h t e c al p s e k at n oit a zi r al o p l a ci rt c e l e e h T

s a ti o t d e t al e r si d n a D s a t i n u e m a s e ht s a h ti e c a p s e e rf ot d e r a p m o c s a l ai r et a m e ht f o e c n e s e r p e h t m o rf g ni si r a y ti s n e d x ul f l a n o iti d d a e ht s e r u s a e m n oi t a zi r al o p e ht s A

si si h T . dl ei f d e il p p a e h t f o n o i t c e ri d e h t ni l a i r e t a m ci r t c e l e i d e h t ni t n e m o m el o pi d t e n e h t ni s tl u s e r h ci h w d l ei f ci rt c el e d e il p p a e h t ot e u d d e c u d n i e r a s el o pi d sl ai r e t a m ci rt c el e i d r al o p n o n nI

si si h T .l ai r et a m ci rt c e l ei d s s o r c s p ol e v e d t n e m o m e l o pi d t e n e c n e h d n a n oi t c e ri d dl ei f e h t ni n g il a ot d n et s el o pi d l l a d e il p p a si d l eif c i rt c e l e l a n r et x e e ht n e h W , s l ai r e t a m ci rt c e l e i d r a l o P nI

ENGINEERING PHYSICS

Dept. of Physics, Jain University

slairetam cirtceleid ralop-non fo noitaziralop

s a re am c r ce e d ra op o no az ra op s a re am c r ce e d ra op o no az ra op sllllaiiiirettttam ciiiirttttcelllleiiiid rallllop ffffo noiiiittttaziiiirallllop s a re am c r ce e d ra op o no az ra op

0 r E = 0 E + P P = 0 ( r 1) E

Since D = 0 r E

0 E

D = 0 E + P

Also

Where is Electric susceptibility

= ( r 1) =

PH14/24

65

noitaziralop cinortcelE )1

. n oi t a zi r al o p e g r a h c e c a p S . n o it a zi r al o p n oi t at n ei r O . n oi t a zi r a l o p ci n oI . n oi t a zi r a l o p ci n o rt c el E

.4 .3 .2 .1

smsinahcem noitaziraloP lacirtcelE

e ht

e ht

. n o it a ti g a l a m r e ht e u d d et n ei r o yl m o d n a r e r a s el o p i d e ht s ci rt c el ei d r a l o p nI . s e l o pi d ci rt c el e t n e n a m r e p s e s s e s s o p h ci h w ,l ai r e t a m ci rt c e l e i d r a l o p ni s r u c c o si h T - :

. e m ul o v ti n u r e p t n e m o m e l o p i d ci n oi y b n e vi g si n oi t a zi r al o P ci n oI

. ht g n e rt s d l e if d ei l p p a e ht o t l a n o it r o p o r p o sl a t n e m o m el o p i d ci n o i e ht t a ht d n u of si tI

e h t f o t n e m o m el o p i d t e n e ht e c n e H

. s e s a e r c ni r e ht r uf s n oi e ht n e e wt e b n oi t a r a p e s e h t d e il p p a si

dl e if ci rt c e l e l a n r e t x e e ht n e h w t u B . d l eif ci rt c e l e l a n r et x e f o e c n e s b a e ht n i n e v e t n e m o m el o pi d t e n s s e s s o p s d il o s ci n oI . ct e e di r ol h c m ui d o s s a h c u s s d il o s ci n o i ni s r u c c o si h T - :

ENGINEERING PHYSICS

Dept. of Physics, Jain University

. s e s a e r c ni o sl a l ai r et a m

noitaziralop cinoI )2

The electronic polarizability is given by e =

Pe = N e = N e E

electronic dipole moment = e = 4 0 R 3 E

E = 0.

E<0

where e electronic polarizability.

e E e = e E

hence

where N is no. of atoms per unit volume.

hence

where i is ionic polarisability.

where is N number of atoms per m 3

pi = N i

E>0

i = i E

0 ( r 1)

E > 0.

PH14/24

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no az ra oP no a ne rO )3 no az ra oP no a ne rO )3 noiiiittttaziiiiralllloP noiiiittttattttneiiiirO )3 no az ra oP no a ne rO )3

n e vi g si t n e m o m el o pi d e h T . g if ni n w o h s s a x d e c n at si d l l a m s a y b d et a r a p e s q d n a q + s e g r a h c hti w e l o p i d a r e di s n o C :

sd uq L dna sd oS o esac n d e anre n ro no sserpxE sd uq L dna sd oS o esac n d e anre n ro no sserpxE sdiiiiuqiiiiL dna sdiiiilllloS ffffo esac niiii dlllleiiiiffff llllanrettttnIIII roffff noiiiisserpxE sd uq L dna sd oS o esac n d e anre n ro no sserpxE
d e ll a c si dl eif t e n si h T .

ro

tniop taht gnidnuorrus selopid lla ot eud dleif


. s el o pi d ci rt c e l e g n it a e r c d e zi r a l o p

dleif lacoL dleif lanretni eht dna dleif lanretxe fo mus ehT

y b n e vi g s i l ai r e t a m ci rt c el ei d e ht ni ht i w t ni o p y n a t a dl eif ci rt c el e

t e n e ht e c n e H . y ti ni ci v e h t ni d l e if ci rt c e l e st e s e l o p i d h c a E

si ti , dl eif ci rt c el e l a n r et x e e ht ni d e c al p si l a i r e t a m ci rt c el ei d n e h W -:

dleiF lacoL ro dleiF lanretnI

.s

P P P P

y b d et o n e d si tI . d et c e l g e n e b n a c ti ll a m s y r e v si si ht

e c n i S .l ai r e t a m e ht s s o r c a t n e m o m el o pi d t e n f o t n e m p ol e v e d e ht ot s d a el si h T . l ai r et a m ci rt c el ei d e ht f o e c af r u s e h t n o e g r a h c e g a m i ri e ht e c u d n i s e g r a h c d e zi l a c o l e s e h T . s e g r a h c d e zi l a c o l d ell a c e r a e s e h T . st c e f e d e citt al t s n i a g a p u e li p r o d e p p a rt t e g y e h t n o it o m ri e ht g ni r u D . e v o m s r ei r r a c e g r a h c e s e ht d eil p p a si d l e if ci rt c el e l a n r et x e e h t n e h W . s e c n a t si d ll a m s h g u o r ht g ni v o m f o el b a p a c

e r a s r ei r r a c e g r a h c w ef a yl n o h ci h w ni sl a i r et a m ni s r u c c o si h T - :

no az ra op egrahc ecapS )4 no az ra op egrahc ecapS )4 noiiiittttaziiiirallllop egrahc ecapS )4 no az ra op egrahc ecapS )4

.t n e m o m el o pi d t n e n a m r e p si d n a e r u t a r e p m e t et ul o s b a si

y b n e vi g si y ti li b a zi r a l o p n o it a t n e i r o e h T

.t n e m o m el o pi d e ht e b ll i w r e ll a m s n oi t at n ei r o el o pi d ni s s e n m o d n a r e h t e r o m e r u t a r e p m et e ht r e h g i H n o s d n e p e d n oi t a zi r a l o p n oit at n ei r O .)o . er ut ar e p m et

P P P P

( n o it a zi r al o p n oit a t n e i r o s a ot d e r r e f e r si si h T

.l a i r et a m e ht s s o r c a s p o l e v e d t n e m o m e l o p i d e r o f e r e h T . n o it c e ri d d l ei f e ht ni n gi l a ot d n e t s el o pi d l l a d e il p p a si d l eif c i rt c el e l a n r e t x e e h t n e h w t u B . o r e z si l ai r e t a m e h t f o t n e m o m el o p i d t e n e r of e r e h T

0 =

ENGINEERING PHYSICS

T T T T

,t n at s n o c n a m ztl o B si e r e h W

k k k k

. e l o p i d f o r e t n e c e h t m o rf r e c n a t si d a t a P t n i o p a r e di s n o C . x d q =

Dept. of Physics, Jain University


yb

3k T

E = 0.

E > 0.

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ni n w o h s s a n oit c e r i d dl ei f e h t n i d e n gi l a e r a h ci h w ,l ai r e t a m ci rt c el ei d e h t ni hti w s el o p i d t n a t si di u q e f o y a r r a n a r e di s n o C . E ht g n e rt s f o dl eif ci rt c el e l a n r et x e ni d e c al p l ai r et a m ci rt c el ei d a r e di s n o C

. el o p i d d n a t ni o p e ht n e e wt e b e c n at si d e ht si r d n a e c a p s e e rf f o yti vit i m r e p si 0 , P t n i o p e h t h ti w el o pi d e ht g ni ni oj e ni l e h t d n a e l o pi d e h t n e e wt e b e l g n a e ht si e r e h W

l ai d a R e ht ot r al u ci d n e p r e p t n e n o p m o c e s r e v s n a r T r o t n e n o p m o c l ait n e g n a T e h T

y b n e vi g si tI . t ni o p e ht d n a e l o pi d e ht g ni ni o j e ni l e ht g n ol a t n e n o p m o C l a i d a R e h T

. st n e n o p m o c o wt ot n i d e vl o s e r e b n a c P t a E d l ei f ci rt c el e e h T

ENGINEERING PHYSICS

Dept. of Physics, Jain University


y b n e vi g si t n e n o p m o c )2

r 2 Cos Er = 4 0 r 3

-q

r Sin E = 4 0 r 3

3a

2a

dx

2a

Err

+q

3a

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. e r u gi f e ht

)1

y b n e vi g si F d n a D s e l o p i d t n at si di u q e ot e u d X t a dl ei f l at ot e ht , yl r al i m i S

y b n e vi g si E d n a C s e l o p i d t n at si di u q e ot e u d X t a d l ei f l at o t e h t , yl r al i m i S

y b n e vi g si B d n a A s e l o p i d t n at si di u q e ot e u d X t a dl ei f l a t o T e ht e c n e H

. y a r r A e ht ni s e l o p i d ll a e u d X t a dl ei f l a c ol e ht d ni f s u t e L

ENGINEERING PHYSICS

Dept. of Physics, Jain University


y b n e vi g si B e l o p i d o t e u d X t a dl e if e h T y b n e vi g si A e l o p i d o t e u d X t a dl e if e h T

E3 =

E3 =

E2 =

E2 =

Hence Er =

Here r = a and = 0 o

Hence Er =

Here r = a and = 180 o

EXA =

EXB =

E1 =

E1 =

+ 2 0 (3a)3 2 0 (3a)3

+ 3 2 0 (2a) 2 0 (2a)3

0 (3a)3

E1 = EXA + EXB

+ 3 2 0 a 2 0 a3

E3 = EXE + EXF

0 (2a)3

2 0 a3

E2 = E XC + E XD

2 0 a3

E XB = Er + E

2 Cos180o

0 a3

4 0 ( a)

EXA = Er + E

2 Cos0 o , E = 0. 4 0 a3

(Q r = 3a)

(Q r = 2a)

, E = 0.

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69

e ht N e r e h w ( N y b 3 a/ 1 g n i c al p e r y b d e zil a r e n e g e b n a c n oi t a u q e e v o b a e ht n oi s n e m i D - e e r h T r o F

y b n e vi g si y a r r a e ht n i s el o pi d l l a ot e u d X t a d l e if t e n e h T

ENGINEERING PHYSICS

E| =

E| =

but

E| = E1 + E2 + E3 + E4 + L L L

1 1 1 + 23 + 33 + L L L 1 = 0 a3 n =1 n3

n=1

+ + + LLL 3 3 0 a 0 (2a) 0 (3a)3

Wkt = E. 1.2 E Ei = E + 0 a3

The Local Field at ' X' is given by 1.2 E i = E + E| = E + 0 a3

1 .2 0 a3

0 a3

1.2

.t n a t s n o C dl ei F l a n r e t nI d el l a c

yb

/ 2. 1 d n a , ) e m ul o v ti n u r e p s m ot a f o r e b m u n

Ei = E +

but polarization P = NE Ei = E +

NE 0

P 0

d el l a c si dl eif l a c o L e h t d n a 3 / 1 =

e ci tt a L ci b u C a r o F . E > i E s e iti t n a u q e vi ti s o p e r a

Dept. of Physics, Jain University

EL = E +

P 3 0

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y b n e vi g si t I . dl ei f zt n e r o L d na , e c ni S

) 2( d n a ) 1( s n o it a u q e g n it a u q E

w ol e b n e vi g s a h t g n e rt s dl eif d ei l p p a e ht o t d et al e r si n o it a zi r al o p e h T

si P n o it a zi r al o p e ht e c n e H . o r e z e r a s ei ti li b a zi r al o p n o it a t n e i r o d n a ci n oi e ht , sl a i r et a m h c u s r of , s el o p i d ,t n e n a m r e p s e s s o p t n o d y e ht e c n i S . l a i r et a m ci rt c el ei d d il o s l at n e m e l E n a r e di s n o C

ENGINEERING PHYSICS

N e P 1 = N e E 3 0 N e E P = ...............eqn(1) N e 1 3 0

P = N e E L

P = N e E + 3 0 P P = N e E + N e 3 0

Where E L is Lorentz Field

f o yti vi tti m r e p si

yti li b a zi r a l o p ci n o rt c e l e si

0 r E = 0 E + P P = 0 ( r 1) E ................... eqn ( 2)

Since D = 0 r E

. ht g n e rt s d l eif ci rt c el E e ht si E d n a , e c a p s e e rf

, e m ul o v ti n u r e p s e l o pi d f o . o n e ht si N e r e h W

D =0 E + P

t n at s n o C ci rt c el ei D si

d n a yti s n e D x ul F ci rt c e l E si D e r e h W

Dept. of Physics, Jain University


P =
N e N e E = 1 0 ( r 1) E 3 0 N e E N e + =1 0 ( r 1) E 3 0

N e E = 0 ( r 1) E N e 1 3 0

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71

y b n e vi g

:noitaleR ittosoM-suisualC -suisualC

noitaziralop cinort cele ylno yllaniF .zH4101 ot zH ci n o i eh T .r e ht o n a r etf a en o e sae c ot tr at s

1 101

s m si n a h c e m

si ycneuqerf eht sA.zH1101 ot zH

601

e g n a r y c n e u q e rf e ht ni s r u c c o si h T . n oi t a x al e r ci rt c el ei d o t e u d

s e s a e c n o it a zi r al o p n oi t at n ei r O s s e c o r p r al u c e l o m e ht e c n e h d n a dl eif e ht ni s n oi t a n r e tl a e ht w ol l of o t el b a n u yl et e l p m o c e r a y e ht r e ht r uf d e s a e r c ni si y c n e u q e rf e ht fI . d l eif f o e s o ht d n i h e b g a l s el o pi d

f o s n o it a lli c s o e ht ) z H M 1 n a ht r et a e r G ( y c n e u q e rf h gi h f o s n o iti d n o c dl ei f g n it a n r etl a r e d n U

. cit at s s ni a m e r t n at s n o c ci rt c el e i d e ht e c n e h d n a d l e if e ht f o s n o it a n r etl a e h t w o ll of n a c n oi t a zi r a l o p e h t n e ht , ) z H M 1 n a ht s s e l ( w o l si dl e if e ht f o y c n e u q e rf e ht fI . s e g n a h c yti r a l o p e ht s a e s r e v e r

ot d n e t n o it a zi r a l o p e ht d l ei f g ni t a n r et l a ni d e c al p e r a sl ai r et a m ci rt c el e i d n e h W . yti t n a u q x e l p m o c a si t n at s n o c c i rt c el ei d e h t , y c n e u q e rf h gi h f o s n o iti d n o c dl ei f g n it a n r e tl a r e d n u d n u of si tI

::)ttnattsnoc ciiirttcellleiiid xelllpmoc & ssolll ciiirttcellleiiiD ,,ttnattsnoc -:)tnatsnoc cirtceleid xelpmoc & ssol cirtceleiD ,tnatsnoc :)tnatsnoc c rtce e d xe pmoc & sso c rtce e D ,tnatsnoc ) na snoc c r ce e d xe pmoc & sso c r ce e D na snoc ciiiirttcelllleiiiiD ffo ecnedneped ycneuqerF (snoiiiittiiiidnoc dlllleiiiiff gniiiittanrettlllla rednu sciiiirttcelllleiiiiD ffo seiiiittreporP c r ce e D o ecnedneped ycneuqerF (sno dnoc d e gn anre a rednu sc r ce e D o se reporP c rttce e D ffo ecnedneped ycneuqerF (sno tt dnoc d e ff gn ttanrett a rednu sc rttce e D ffo se ttreporP c r ce e D o ecnedneped ycneuqerF (sno dnoc d e gn anre a rednu sc r ce e D o se reporP
. d e n i m r e t e d e b n a c yti li b a zi r a l o p ci n o rt c e l e e ht n e ht n w o n k si l ai r et a m e ht f o t n a t s n o c ci rt c el ei d f o e ul a v e h t fi n o i t a l e r e v o b a e h t g ni s U . n oi t al e r i t t o s o M s ui s u al C d e ll a c si n o i t a u q e e v o b a e h T

ENGINEERING PHYSICS

Dept. of Physics, Jain University


e g n a r y c n e u q e rf e ht n i s e s a e c n oi t a zi r a l o p g ni zi r al o p r e ht o r e htr uf d e s a e r c ni

Polarization

Space Charge

Orientation

Electronic

Ionic

N e 3 0

N e r 1 = + 2 3 0 r

3 ( 1) + 1 = 1 r

Frequency

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72

. s r o t a r bi v d n a s r o t al li c s o ni d e s u e r a sl at s y r c ci rt c e l e o z ei P . s r oti c a p a c e g a r ot s y g r e n e e ht ni d e s u e r a sl a i r et a m ci rt c el ei D . s r e m r of s n a rt n i s r ot al u s n i d e s u si n ott o c d e h si n r a V . y d o b r e t u o ot t n e r r u c ci rt c el e f o w ol f e h t t n e v e r p o t r e d r o ni n o r I ci r t c e l e ni d e di v o r p si n oi t al u s ni s o t s e b s A d n a a ci M . n o it a l u s n i f o e s o pr u p e h t r of o sl a d n a g nit i u c ri c t r o h s ci r t c el e f o n o it n e v e r p e ht r of d e s u e r a s d a e b ci m a r e C s r ot c u d n o c l a ci rt c el e f o s n oit al u s n i e ht r o f d e s u e r a c i rt c el e i d r e b b u R d n a ci t s al P

s n oi t a cil p p a f o e g n a r e di w a d n i f sl ai r e t a m c i r t c el ei D

s a d ell a c si si h T .l ai r et a m e ht y b t a e h s a d et a pi s si d si h ci h w , n o it ci rf l a n r e t ni f o t r o s e m o s e m o c r e v o o t e v a h y e ht s el o pi d f o n oi t at o r e ht g ni r u d s n oi ti d n o c d l ei f g nit a n r etl a e ht nI - :

no sreps D c rttce e D suo amonA no sreps D c r ce e D suo amonA noiiiisrepsiiiiD ciiiirttcelllleiiiiD suollllamonA sa nwonk si sihT no sreps D c r ce e D suo amonA

e ht e c n e h d n a s e s a e r c e d n oit a zi r al o p e ht s e s a e r c ni dl ei f e ht f o y c n e u q e rf e ht s a e c n e H . s n i a m e r

ENGINEERING PHYSICS

PH14/24

er e h W

.r

*r

y b n e vi g si t n at s n o c ci rt c e l ei d x el p m o c e h T - :

. s e s a e r c e d t n a t s n o c ci rt c el ei d

e ht hti w

09 yb

e s a h p f o t u o t n e r r u c f o t n e n o p m o c e ht s e ni m r e t e d

Dept. of Physics, Jain University


)6 )5 )4 )3 )2 )1 . sl ai r e t a m g ni t al u s ni s a

73

:slairetaM cirtceleiD fo snoitacilppa tnatropmI


. dl eif

. s s o L ci rt c e l e i D s e ni m r et e d

ttnattsnoC c rttce e D xe pmoC na snoC c r ce e D xe pmoC ttnattsnoC ciiiirttcelllleiiiiD xellllpmoC na snoC c r ce e D xe pmoC
. s s ol ci rt c el ei d

ssoL cirtceleiD

ENGINEERING PHYSICS

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MODULE V
ELECTRICAL CONDUCTIVITY IN METALS
Classical free electron theory of metals: In order to explain electrical conductivity in metals, Lorentz and Drude put forward a theory called free electron theory of metals. It is based on the following assumptions. 1. Free electrons in a metal resemble molecules of a gas. Therefore, Laws of kinetic theory of gasses are applicable to free electrons also. Thus free electrons can be assigned with average velocity c, Mean free path and mean collision time . 2. The motion of an electron is completely random. In the absence of electric field, number of electrons crossing any cross section of a conductor in one direction is equal to number of electrons crossing the same cross section in opposite direction. Therefore net electric current is Zero. 3. The random motion of the electron is due to thermal energy. Average kinetic energy of the electron is given by

Where c=average velocity or thermal velocity 4. Electric current in the conductor is due to the drift velocity acquired by the electrons in the presence of the applied electric field. 5. Electric field produced by lattice ions is assumed to be uniform throughout the solid. 6. The force of repulsion between the electrons and force of attraction between electrons and lattice ions is neglected. The Drift Velocity : In the absence of the applied electric field, motion of free electron is completely random. During their motion electrons undergo collisions with the residual ions and during each collision direction and magnitude of their velocity changes in general. When electric field is applied, electrons experiences force in the direction opposite to the applied field. Therefore in addition to their random velocity, electron acquires velocity in the direction of the force. Since electrons continue to move in their random direction, with only a drift motion due to applied field, velocity acquired by the electrons in the direction opposite to the applied field is called Drift velocity and is denoted by vd. Note the vd is very small compared to c, the average thermal velocity. Electric current in a conductor is primarily due to the drift velocity of the electrons. Electronic Conduction in Solids Relaxation Time, Mean collision time and Mean free path: Mean free path (): The average distance traveled by electrons between two successive collisions during their random motion is called mean free path, it denoted by . Mean collision Time(): The average time taken by an electrons between two successive collisions during their random motion is called mean collision time, it is denoted by . The relationship between and is given by =c.

Dept. of Physics, Jain University

74

ENGINEERING PHYSICS

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Relaxation Time(r): In the presence of an applied electric field, electrons acquire drift velocity vd in addition to the thermal velocity c. if electric field is switched off, vd reduces and becomes zero after some time. Let electric field is switched off at the instant t = 0, when drift velocity vd=v0. The drift velocity of the electron after the lapse of t seconds is given by

Where r is called relaxation time. Suppose t=r , then vd=v0 , e-1=1/ev0 Thus the relaxation time is defined as the time during which drift velocity reduces to 1/e times its maximum value after the electric filed is switched off.

Dept. of Physics, Jain University

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HALL EFFECT
Suppose a material carrying an electric current is placed in a magnetic field. Then an electric field is produced inside the material in a direction which is at right angles to both the current and magnetic field. This is called Hall effect discovered by Edwin H. Hall in 1879.

Let us consider a metal. Let the current J be in the X direction as shown in figure. The current carriers which are the free electrons in the metal have a drift velocity v in the negative X direction. Let a magnetic field B be applied along the Z direction. Then the electrons will experience a force of magnitude Bev. The direction of the force is by Flemings left hand rule in the negative Y direction. This force is called Lorentz force. Under the action of this force the free electrons will move in the negative Y direction and collect on the bottom surface of the material. There will be a deficit of electrons on the top surface. This is equivalent to a collection of positive charges on the top surface. The collection of positive

Dept. of Physics, Jain University

88

ENGINEERING PHYSICS

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and negative charges on the top and bottom faces of the material results in an electric field in the negative Y direction. This electric field is called Hall field. If its magnitude is EH the force due to it on an electron is eEH in the positive Y direction. This force opposes the Lorentz force. Soon an equilibrium condition will set up when

eE H = Bev .(1)
If the current density in the X direction is J then,

J = nev ..(2)
Where n is the concentration of the free electrons. Then by combining (1) & (2) we get

EH =
Or

BJ ne

E H = RH JB 1 Where R H = ne

is called the Hall coefficient.

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MODULE VI
MAGNETIC PROPERTIES OF SOLIDS
Classification of Diamagnetic, Paramagnetic and ferromagnetic materials Diamagnetic Materials The substances which tend to move from stronger to weaker region of the magnetic field are called diamagnetic substances. These are weakly repelled by a strong magnet. In these substances, there are equal numbers of electrons spinning and orbiting in opposite directions so that the electrons of an atom remain paired in such away that their net magnetic moment is zero in the absence of any external magnetic field. Examples: Antimony, bismuth, copper, gold, lead, mercury, silver etc Properties 1. The relative permeability is less than unity 2. The susceptibility is negative 3. The susceptibility does not vary with temperature. Paramagnetic Materials The substances which tend to move from weaker to stronger regions of magnetic field are called paramagnetic substances. These are feebly attracted by a strong magnet. In these substances, the atoms or molecules with one or more unpaired electrons possess a permanent magnetic moment. But they are oriented randomly in the absence of an external magnetic field. Examples: Aluminium, chromium, manganese, platinum, sodium etc Properties 1. Low magnetization, low susceptibility 2. Susceptibility is small, positive and varies inversely with temperature 3. Permeability is greater than one

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Paramagnetic susceptibility =

C Where C is curie constant T

This result namely the magnetic susceptibility of atoms varies as

1 T

is known as Curies law.

Ferromagnetic materials The substances which are strongly attracted by a magnet are called ferromagnetic substances. These are the permanent magnets which exhibit hysteresis. It arises due to the self alignment of groups of atoms carrying permanent magnetic moment in the same direction. The magnetic moment is an account of spin of the electrons. Ferromagnetic materials are characterized by curie temperature

above which they become paramagnetic materials. Examples: iron, cobalt, nickel and their alloys. Properties 1. The relative permeability is very high 2. The susceptibility is very high and it depends on the temperature. 3. They exhibit magnetostriction and hysteresis

Ferromagnetic susceptibility =

C (T )

Where C is curie constant

B H Curve ( Hysterisis)

Br -Hc

Bsat

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1. A ferromagnetic solid can be assumed to be comprised of small number of small regions called domains each of which is spontaneously magnetized. The magnetic moments of all the exams are all aligned in a particular direction. However the different domains are so oriented as to make the net magnetization zero. 2. The process of magnetization consists in rotating the different domains in the direction of applied field so that the specimen exhibits net magnetization. 3. When a magnetic field is applied on a ferromagnetic material, the domains nearly parallel to H can grow in size at the expense of antiparallel domains and gradually all the domains align along the applied field at which the material is said to be saturated. The hysteresis can be explained as follows. 1. As H is further increased, the rate of increase of B falls and ultimately becomes zero and the flux density B reaches a saturation value indicated as Bsat in the figure. 2. As the applied field H is reduced from the saturation value to zero, the reduction of flux density does not follow the same path. 3. When H becomes zero, their remains certain amount of flux in the material called the remnant flux density Br . The material remains magnetized even in the absence of an external field. 4. To reduce the remnant flux Br to zero, it is necessary to apply H in the reverse direction and the amount Hc required to make Br zero is called the coercive force. 5. As the field is increased beyond Hc , the flux density reaches saturation. 6. When a ferromagnetic material is taken over one cycle of magnetic field, it exhibits hystresis loop. 7. The area of the hystresis loop signifies the amount of energy required for magnetization.

Soft magnetic materials:


Magnetic materials that have high permeability and low coercive force are called soft magnetic materials.

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These are temporary magnets which can retain magnetism for a short interval of time. They possess small hysteresis loss. Properties: 1. Low remnant magnetism 2. High permeability 3. High susceptibility 4. Low coercivity 5. Low hysteresis energy loss 6. Thin hysteresis loop 7. Low eddy current loss Ex: Soft iron, mild Steel, Sendust, perm alloy, pure nickel Uses: 1. They are used in the construction of cores of transformers. 2. Relatively pure iron is frequently used as the magnetic core for direct current applications. 3. The magnetic mild steel is used for relays, reed switches and pole pieces for electromagnets. 4. Iron-nickel alloys are used for audio frequency applications.

Hard magnetic materials :


Magnetic materials that have large energy product (BH) and high coercivity are called hard magnetic materials.

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Properties:
1. Large hysteresis loop 2. High coercivity 3. High remanent magnetization 4. High permeability 5. High hysteresis energy loss 6. High saturation flux density Ex: Carbon, tungsten-steel alloy, alloy steel, alloys of aluminium Uses: 1. The permanent magnets are used in instruments like galvanometers, ammeters, voltmeters, speedometers and recorders. 2. Tungsten steel are used in chucks and latches, tool holders, magnetic bearings and mixers. 3. They are used in electronic devices such as telephones and tape recorders, loud speakers and hearing aids.

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Superconductivity: Temperature dependence of resistivity of metal

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The variation of resistivity with temperature for a metal is as shown in the fig. Resistivity in the case of pure metal decreases with the decrease in temperature and becomes zero at absolute zero temperature. While in the case of impure metals the resistivity of metal will have some residual value even at absolute zero temperature. This residual resistance depends only on the amount of impurity present in the metal and is independent of the temperature.

Thus net Resistivity of a metal can be written as


= 0+ (T)
Thus net Resistivity of conductor is equal to sum temperature independent part and temperature dependent part as shown in the graph Superconductivity Kamerlingh Onnes discovered the phenomenon of superconductivity in the year 1911. When he was studying the temperature dependence of resistance of Mercury at very low temperature he found that resistance of Mercury decreases with the decrease in temperature up to a particular temperature Tc= 4.15K . Below this temperature the resistance of mercury abruptly drops to zero. Between 4.15K and Zero degree Kelvin Mercury offered no resistance for the flow of electric current. The phenomenon is reversible and material becomes normal once again when temperature was increased above 4.15K. He called this phenomenon as superconductivity and material which exhibited this property as superconductors.

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Thus the phenomenon of super conductivity is defined as: The phenomenon in which resistance of certain metals, alloys and compounds drops to zero abruptly, below certain temperature is called superconductivity The temperature, below which materials exhibit superconducting property is called critical temperature, denoted by Tc. Critical temperature Tc is different for different substances. The materials, which exhibit superconducting property, are called

Superconductors. Above critical temperature material is said to be in normal state and offers resistance for the flow of electric current. Below critical temperature material is said to be in superconducting state. Thus Tc is also called as transition temperature. Meissner Effect In 1933, Meissner and Ochsenfeld showed that when a superconducting material is placed in a magnetic field, it allows magnetic lines of force to pass through, if its temperature is above Tc and if temperature is reduced below the critical temperature Tc, it expels all the lines of force completely out of the specimen to become a perfect diamagnetic material. This is known as Meissner effect. Since superconductor exhibits perfect diamagnetism below the critical temperature Tc, magnetic flux density inside the material is zero. Therefore B=0, for T< Tc

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Relationship between flux density and the strength of the magnetizing field is given by

0 = Absolute permeability of free space


M = Intensity of magnetization of the material & H = Strength of the magnetizing field

Thus superconductor possesses negative magnetic moment when it is superconducting state.

Consider a superconducting material above its critical temperature. A primary coil and secondary coil are wound on the material. The primary coil is connected to battery and the

secondary coil is connected to a Ballistic Galvanometer. When the primary circuit is closed, current flows through it, which sets up a magnetic field in it. The magnetic flux immediately links with the secondary coil. This change in flux across the secondary coil produces the momentary current and hence the galvanometer shows the deflection.

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After certain time, the primary current becomes steady; flux linkage with the secondary coil becomes unchanging. As a result, no change in the flux linkage in the secondary coil and hence no more current driven in the secondary circuit. Now, decreases the temperature of the super conductor gradually. As soon as the

temperature crosses below the critical temperature, the B.G. suddenly shows a deflection, indicating that the flux linkage with the secondary coil has changed. The change in flux linkage is attributed to the expulsion of the magnetic flux from the body of the superconducting material as shown in figure.

Critical field We know that when superconductor is placed in a magnetic field it expels magnetic lines of force completely out of the body and becomes a perfect diamagnet. But if the strength of the magnetic field is further increased, it was found that for a particular value of the magnetic field, material looses its superconducting property and becomes a normal conductor. The value of the magnetic field at which superconductivity is destroyed is called the Critical magnetic field, denoted by Hc. It was found that by reducing the temperature of the material further superconducting property of the material could be restored. Thus, critical field doesnt destroy the superconducting property of the material completely but only reduces the critical temperature of the material

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Critical magnetic field Hc depends on the temperature of the material. The relationship between the two is given by

Isotopic effect The variation of critical temperature of an element with isotopic mass is called isotopic effect. The transition temperature is inversely proportional to the square root of the atomic mass of the isotope of a single superconductor.

TC
Critical current density

1 Ma

a= constant equal to , M= atomic weight

The application of a large value of electric current to superconducting material destroys the superconducting property. Consider a coil of wire wound on superconductor .Let I be the current Flowing through the wire. The application of the current induces a magnetic field. Thus, induced Magnetic field in the conductor destroys the superconducting property. The induced critical current is given by

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Ic = 2rHc Ic=critical current density Hc= critical field BCS theory of Superconductivity

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Bardeen, Cooper and Schrieffer explained the phenomenon of superconductivity in the year 1957. The essence of the BCS theory is as follows. We know that resistance of the conductor is due to the scattering of electrons from the lattice ions. Consider an electron moving very close to a lattice ion. Due to coulomb interaction between electron and ion, the ion core gets distorted from its mean position. It is called lattice distortion. Now another electron moving close to this lattice ion interacts with it. This results in the reduction in the energy of the electron. This interaction can be looked upon as equivalent to the interaction between two electrons via lattice. During the interaction exchange of phonon takes place between electron and the lattice. This interaction is called electron-lattice electron interaction via the phonon field. Because of the reduction in energy between the two electrons, an attractive force comes into effect between two electrons. It was shown by Cooper that, this attractive force becomes maximum if two electrons have opposite spins and momentum. The attractive force may exceed coulombs repulsive force between the two electrons below the critical temperature, which results in the formation of bound pair of electrons called cooper pairs. At temperatures below the critical temperature large number of electron lattice- electron interaction takes place and all electrons form a cloud of cooper pairs. Cooper pairs in turn move in a cohesive manner through the crystal, which results in an ordered state of the conduction electrons without any scattering on the lattice ions. This results in a state of zero resistance in the material. Persistent current Once a current is started in a closed loop of superconducting material, it will continue to keep flowing of its own accord, around the loop as long as the loop is held below the critical temperature. Such a steady current Which flows with undiminishing strength is called a persistent current. The persistent current does not need external power to maintain it because there does not exist I2R losses. In one instance, a current is maintained in a superconducting loop for more than two years. Persistent current is one of the most

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important properties of a superconductor. Superconductor coils with persistent currents produce magnetic fields and can therefore serve as magnets. Such a superconducting magnet does not require a power supply to maintain its magnetic field. Types of Superconductors Type I or Soft Superconductors: Superconducting materials, which exhibit, complete Meissner effect are called Soft superconductors. We know that below critical temperature, superconductors exhibit perfect diamagnetism. Therefore they possess negative magnetic moment.

The graph of magnetic moment Vs magnetic field is as shown in the Fig. As field strength increases material becomes more and more diamagnetic until H becomes equal to Hc. At Hc, material losses both diamagnetic and Superconducting properties to become normal conductor. It allows magnetic flux to penetrate through its body. The value of Hc is very small for soft superconductors. Therefore soft superconductors cannot withstand high magnetic fields. Therefore they cannot be used for making superconducting magnets Type II or Hard Superconductors Superconducting materials, which can withstand high value of critical magnetic fields, are called Hard Superconductors.

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The graph of magnetic moment Vs magnetic field is as shown in the Fig. Hard superconductors are characterized by two critical fields Hc1 and Hc2. When applied magnetic field is less than Hc1 material exhibits perfect diamagnetism. Beyond Hc1 flux penetrates and fills the body partially. As the strength of the field increases further, more and more flux fills the body and thereby decreasing the diamagnetic property of the material. At Hc2 flux fills the body completely and material losses its diamagnetic property as well as superconducting property completely. Between Hc1 and Hc2 material is said to be in vortex state. In this state though there is flux penetration, material exhibits superconducting property. Thus flux penetration occurs through small-channelised regions called filaments. In filament region material is in normal state. As Hc2 the field strength increases width of the filament region increases at they spread in to the entire body, and material becomes normal conductor as a whole. The value of Hc2 is hundreds of times greater than Hc of soft superconductors. Therefore they are used for making powerful superconducting magnets.

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Applications of Superconductivity 1. Superconducting Magnets:

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We know that in ordinary electromagnet strength of the magnetic field produced depends on the number of turns (N) in the winding and the strength of the current (I) flowing through the winding. To produce strong magnetic field either N or I should be increased. If N is increased size of the magnet increases and if I is increased power loss (I2R) increases, which results in production of heat. Therefore there are limitations to increase N and I. If superconducting wires are used for winding in electromagnets, even with small number of turns strong magnetic fields can be produced by passing large current through the winding, because there is no loss of power in superconductors. The type II superconductors, which have high Hc and Tc values, are commonly used in superconducting magnets. Ex: Niobiumtin, Niobium-aluminum, niobium-germanium and vanadium-gallium alloys. The superconducting magnets are used in Magnetic Resonance Imaging (MRI) systems, for plasma confinement in fusion reactors, in magneto-hydrodynamic power generation, in Maglev vehicles, etc. 2. Maglev (Magnetically Levitated vehicles)

1. In these vehicles transportation is by setting afloat the carriage above the guide way. 2. Utility of such levitation is that, in the absence of contact between the moving and stationary systems, the friction is eliminated. 3. Great speed is achieved with low energy consumption.

4. The phenomenon is based on Meissner effect.

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5. The vehicle consists of superconducting magnets built into its base. There is an Aluminium guide way over which the vehicle will be set afloat by magnetic levitation. This is brought about by enormous repulsion between two powerful magnetic fields, one produced by superconducting magnet inside the vehicle and the other one by electric currents in the Aluminium guide way. 6. Guide way is divided into a number of segments provided with coils. The flow of currents through the coils could be related to the position and instantaneous speed of the vehicle. 7. The currents in the guide way not only produce the necessary magnetic field to levitate the vehicle but also help in propelling the vehicle forward. 8. The vehicle is provided with retractable wheels. With these wheels the vehicle runs on the guide way. Once levitated in air the wheels are retracted into the body, while stopping, the wheels are drawn out and vehicle slowly settles on the guide way by running over a distance. 3. SQUID (Superconducting Quantum Interference Device)

It is an ultra-sensitive measuring instrument used for the detection of very weak magnetic fields. (~ 10-14T)

It is formed by incorporating two Josephsons junctions (J1 and J2) in the loop of a superconducting material.

An arrangement consisting of two superconductors separated by a thin oxide layer (insulator) is known as Josephsons junction. When the wavelength of the matter wave generated by the cooper pair is greater than barrier width, cooper pairs from one superconductor can tunnel through the barrier and reach the other superconductor.

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When the magnetic field is applied to this superconducting circuit, it induces a circulating current which produces just that much opposing magnetic field as to exclude the flux from the loop.

The flux remains excluded so long as the junction currents do not exceed a critical value. (Where the critical current IC, which is the maximum current across the junction under zero voltage condition)

But the circuit switches to resistive phase and thereby the flux passes into the loop. Once, the current in either of the junctions or in both exceed the critical value, the loop acts like a gate to allow or exclude the flux.

A mathematical analysis shows that, IC that is supported in the loop is a periodic function of the applied magnetic flux ( ).

Peridoic variation of the critical current IC with the total flux through the area of the squid.
It can be interpreted as the consequence of interference due to the phase difference between the reunited currents. The phase difference is caused by the applied magnetic field. Here both the interference effects and the quantization effects in superconductivity state are involved. Thus the device is named as SQUID. Applications: When the squid is brought under the influence of the external field, the flux through the loop changes. It causes a change in squid current Is. The variation in Is will be periodic in nature and hence induces an emf in an adjacent coil of an electric circuit that senses changes in the flux.

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It can be used to detect magnetic fields of heart and brain. It can be used for logic operations in an electronic circuit as well as memory devices. Temperature dependence of specific heat The specific heat of the normal metal is seen to be of the form.

C n (T ) = T = T 3
The first term in Eq. is the specific heat of electrons in the metal and the second term is the contribution of lattice vibrations at low temperatures. The specific heat of the superconductor shows a jump at Tc. Since the superconductivity affects electrons mainly, it is natural to assume that the lattice vibration part remains unaffected, i.e., it has the same value T3 in the normal and superconducting states. On subtracting this, we notice that the electronic specific heat Ces is not linear with temperature. It rather fits an exponential form.

C es (T ) = A exp( K B T )

Temperature dependence of the electronic specific heat in the normal and superconducting states This exponential form is an indication of the existence of a finite gap is the energy spectrum of electrons separating the ground state from the lowest state.

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The number of electrons thermally excited across the gap varies exponentially with the reciprocal of temperature. The energy gap is believed to be a characteristic feature of the superconducting state which determines the thermal properties as well as high frequency electromagnetic response of all superconductors.

(a) (a) Conduction band in the normal state.

(b)

(b)Energy gap at the Fermi level in the superconducting state E=10 eV.

Thermal Conductivity The thermal conductivity of superconductors undergoes a continuous change between the two phases and is usually lower in the superconducting phase suggesting that the electronic contribution drops, the superconducting electrons possibly playing no part in heat transfer. The thermal conductivity of tin at 2 K is 34W cm-1 K-1 for the normal phase and 16W cm-1 K-1 for the superconducting phase. At 4K, it is 55 W cm-1 K-1 (At 4K there is no superconducting phase for tin as Tc=3.73K).

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Thermal conductivity of a specimen of tin in the normal and superconducting state

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