Dept. of Physics CMR INSTITUTE OF TECHNOLOGY BANGALORE DEPARTMENT OF PHYSICS COURSE MATERIAL ENGINEERING PHYSICS PHY 12/22(NEW SCHEME) External Exam : 100 Marks Internal Test : 25 Marks AUTHOR RAVEESHA.K.H. [email protected]DEPARTMENT OF PHYSICS CMR INSTITUTE OF TECHNOLOGY C.M.R Institute of Technology, Bangalore 1
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Dept. of Physics
CMR INSTITUTE OF TECHNOLOGY
BANGALORE
DEPARTMENT OF PHYSICS
COURSE MATERIAL
ENGINEERING PHYSICS PHY 12/22(NEW SCHEME)
External Exam : 100 Marks Internal Test : 25 Marks
CMR INSTITUTE OF TECHNOLOGYIT PARK ROAD,KUNDALAHALLI
BANGALORE-560037
C.M.R Institute of Technology, Bangalore 1
Dept. of Physics
CONTENTS
Chapter Page No
1. Plancks quantum theory 3
Davisson – Germer experiment 10
Debroglies theory 14
Particle in an infinite potential well 18
2. Crystal physics 21
Expression for interplanar spacing 30
Packing factor 33
3. X – rays 37
4. Electron conduction 43
Density of states 50
5. Magnetic materials 54
6. Superconductivity 61
7. Dielectrics 68
8. Optical properties of solids 78
Ruby laser 83
Helium laser 84
9. Optical fibres 88
10. Holograms 95
CHAPTER 1: Planck’s quantum theory
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Basic definitions:
Opaque objects: They do not transmit any radiation.
Black body : It is an object which absorbs all radiations incident on it and emit those
radiations on heating. Its absorption coefficient is 100%.
White body : It reflects all the incident energy.
Black body :
A good approximation of a black body is a small hole leading to the inside of a hollow object as
shown in the above fig. Any radiation that falls inside through the hole gets reflected in every
direction and finally all the energy is absorbed. The nature of the radiation emitted from the hole
depends only on the temperature of the cavity walls. The distribution of the radiated energy varies
with wavelength and temperature as shown in the following graph.
Features of Black body spectrum:
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Intensity
4000K
3000K
2000K
Wavelength
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Interpretation of the graph:
1. A black body emits over wide range of wavelengths at different temperatures.
2. At each temperature, there exists a wavelength at which maximum energy is radiated.
3. As the temperature increases, the amount of energy radiated (the area under the curve)
increases and the peak shifts towards shorter wavelengths.
4. As temperature increases, energy emitted also increases.
Note:
Stefans law: Total energy radiated per unit area is proportional to the fourth power of the
temperature.
where J/m2/s
Weins displacement law: The product of the wavelength at which maximum energy is radiated
and the temperature is a constant.
Rayleigh –Jeans Law: Intensity of radiation from a hot body is inversely proportional to the
fourth power of the wavelength .
As a consequence, the energy radiated by a hot body must become very high at lower
wavelengths (ultraviolet region) leading to ‘ultraviolet catastrophe’. However, experimentally
the intensity of radiation decreases with decrease in temperature.
Planck’s radiation law:
In 1900, Max Planck developed a structural model for black body radiation that leads to a
theoretical equation for the wavelength distribution that is in complete agreement with the
experimental results at all wavelengths.
According to his theory
1. a black body is imagined to be consisting of large number of electrical oscillators.
2. an oscillator emits or absorbs energy in discrete units. It can emit or absorb energy by making
a transition from one quantum state to another in the form of discrete energy packets known
as photons whose energy is an integral multiple of hν where h is the planks constant and ν is
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the frequency.
3. the key point in Planck’s theory is the radical assumption of quantized energy states. This
development marked the birth of quantum theory.
Based on these ideas, Planck was able to derive an expression that agreed remarkably well
with the experimental curves. It is given by
Deduction of Weins law:
It is applicable at smaller wavelengths.
For smaller wavelengths
So Planck’s radiation law becomes
Deduction of Rayleigh Jeans Law:
It is applicable at longer wavelengths.
For longer wavelengths
Photoelectric effect:
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It is a process in which when an electromagnetic radiation of suitable wavelength is incident on
certain metals, they emit electrons.
Work function: It is the minimum energy required to remove an electron from an atom.
Threshold wavelength: It is a particular wavelength above which photoelectric emission is not
possible.
Stopping potential: It is the negative potential which has to be applied to stop the electrons which
are moving towards the positive electrode.
Laws of photoelectric emission:
1. Photoelectric current is proportional to the intensity of light.
2. For a given metal, there exists certain minimum frequency below which photoelectric
emission is not possible.
3. Kinetic energy of electrons is proportional to the frequency of radiation.
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Quartz bulb
Radiation of suitable wavelength
electrons
Galvanometer
Stopping potential
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4. Rate of emission of electrons is independent of temperarture.
Einstein’s photoelectric equation:
Incident energy = workfunction + kinetic energy
hν = Ф +
Types of photoelectric cells:
1. Photoemissive cell:
2. Photovoltaic cell :
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3.Photo conductive cell :
Note :
If V is the stopping potential , then
eV = kinetic energy =
Einsteins equation becomes
hν = Ф +
Physical significance of photoelectric effect:
1. It supports the quantum theory.
2. It confirms the fact that the light radiation consists of particles called as photons.
Compton Effect:
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Copper sheet
Cu2O film radiation
Metallic bar
Metallic transparent film radiation
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It is an effect in which when x rays are incident on electron, the scattered radiation will have the
wavelength equal to or greater than the incident wavelength.
Change in wavelength of x ray after scattering =
Here h is plancks constant
m0 is rest mass of electron
c is velocity of light
θ is angle of scattering
Physical significance:
It supports the particle nature of light.
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λ1
Incident X-ray of wavelength λ
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DUAL NATURE OF MATTER
Davisson and Germer experiment:
(Davisson and Germer were working at Bell Labs studying structure of crystals)
This experiment confirms the wave nature of electrons.
The apparatus used by Davisson and Germer is shown below. A beam of electrons from a
heated filament ‘F’ is accelerated through a potential difference V .It passes through a narrow
aperture and strikes nickel crystal .Electrons are scattered in all directions by the atoms of the
crystal. These scattered electrons are detected by a device which can be moved to any angle
relative to the incident beam and it can also measure the intensity of the scattered beam.
The results of the experiment are shown in the following graphs.
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F
+, V
Crystal
Detector
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Dept. of Physics
From these graphs, it is clear that initially at 38V, 46V, electrons are scattered uniformly in all
directions. When the accelerating voltage is set at 54V, there is an intense reflection of the beam
at =50˚. This maximum intensity caused at this angle can only be accounted for constructive
interference of electron waves. If we assume that each atom of the crystal acts as a scatterer ,
then all the electron waves which get scattered from different layers of atoms which are in phase
undergo constructive interference producing maximum intensity. By knowing the angle of
maximum intensity and the inter atomic spacing, the wavelength of the electron waves can be
calculated using the relation
where D is the interatomic distance, is the angle between the incident beam and scattered
beam.
For Nickel D=0.215 nm, = 50˚.
λ= 0.215 x sin 50˚ = 0.165 nm
Theoretically, using Debroglie’s law we can calculate the wavelength of the waves associated
with electrons of energy 54ev.
λ= 0.165 nm
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38ev 46ev 54ev 64ev
Spherical polar graphsHere the length of the position vector to a point on the graph is a measure of number of electrons scattered along that vector direction
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The theoretical and experimental values are in excellent agreement. This confirms the existence
of matter waves.
Phase velocity(Vp): It is the speed of a single pulse in a medium. Generally waves observed
in nature like light waves, sound waves, electromagnetic signals etc travel as groups. So phase
velocity is rarely used.
A single pulse ishown in this diagram .It is represented as
Y = A sin [wt – kx]
where Y is the displacement of a particle at a distance ‘x’ from the origin at a time ‘t’, A is the
amplitude , w is the angular velocity and k is the wave number.
Vp =
Group Velocity(Vg): It is the velocity with which the resultant amplitude of group of waves
propagates .
Consider two waves of same amplitude but of slightly different wavelengths travelling in the
same direction.
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Y
X
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Let the waves be represented as
Y1 = A sin (wt – kx) … (1)
Y2 = A sin [(w+Δw) t – (k + Δk) x]
= 2A cos[( )t – ( )x] sin ( )t – ( ) …. (2)
But Δw and Δk are small
2w + Δw 2w, 2k+ Δk 2k
Y = 2A cos [( ) t – ( ) x] sin (wt-kx) .....(2)
Comparing equations (1) and (2), the coefficient of sin (wt-kx) in equation (2) can be considered
as the amplitude of the wave.
Amplitude of the resultant wave =2A cos [(Δw/2) t – (Δk/2) x]
This amplitude varies as a wave .The velocity with which the variation in amplitude is propagated
is referred as group velocity
Vg = (Δw/2) / (Δk/2)
Vg = Δw / Δk =
Note: The energy carried by a wave packet travels at the group velocity, not the phase velocity.
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Y1= A Sin(ωt – kx) Y2 = A sin [(ω+∆ω)t+(K+∆K)x]
Superposition
Resultant Envelope with varying amplitude
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Relation between phase velocity and group velocity:
We have phase velocity Vp =
Vg = = = Vp + K. ………. (1)
But = X and k = ;
Substituting these in equation (1) we get
Vg = Vp -
Relation between group velocity and particle velocity:
By definition Group velocity is Vg = …………………………… (1)
w = 2Πf = 2Π
dw =
k = = 2 ; dk =
Substitute for dw and dk in equation (1)
Vg =
Using the expression E =
Also p = m
=
This shows that Group velocity and Particle velocity are equal.
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Note: The velocity of group of waves representing a particle cannot be different from particle
velocity as both are related to one physical entity.
Relation between Vg, Vp and velocity of light :
Vp =
Vp.
Debroglie’s theory:
Statement: By the law of symmetry of nature, a particle must exhibit wave like properties in
addition to its particle properties.
The wavelength of the group of waves associated with particle of mass m moving with a velocity
v is given by the expression
=
where h is the Planck’s constant
Derivation: According to debroglie theory, a moving material particle is associated with a group
of plane waves .The group velocity of the waves associated with an object of mass m moving
with a velocity v is given by
Vg = ……… (1)
But w = 2 k = ;
dw = 2 dk = 2 . d
Substituting this in equation (1) we get
d = …………………………… (2)
The total energy of the particle is given by
E = m v2 + V where V is the potential energy
The energy present in the waves associated with the particle is given by
E = hf
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Dept. of Physics
Since energy of a particle remains the same either in particle form or the wave form
hf = m v2 + V
If the particle is moving in a region free of fields V = 0
hf = m v2
Differentiating h df = m v dv
df = dv
Substituting this in equation (2)
d =
Integrating
= + Constant
Neglecting the constant.
Heisenberg’s uncertainty principle:
The position and momentum of a particle cannot be determined accurately and simultaneously.The product of uncertainty in position and momentum is always greater than or equal
to .
.
This uncertainty is not due to discrepancy with the apparatus or with the method of measurement, but because of the very wave nature of the object. This uncertainty persists as long as matter possesses wave nature.
Different forms of Heisenberg’s Principle:
.
Here ΔL is the uncertainty in angular momentum
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Δθ is the uncertainty in angular displacement
ΔE is the uncertainty in the energy
Δt is the uncertainty in the time interval during which the particle exists in the state E
Time independent Schrödinger equation
A matter wave can be represented in complex form as
Differentiating wrt x
…………………….. (1)
From debroglie’s relation
=
k = =
………………………. (2)
Total energy of a particle E = Kinetic energy + Potential Energy
E = m v2 + V
Substituting in (2)
From (1)
Significance of :
According to Max Born, is a measure of probability of finding a particle in specified region.
Normalisation: Total probability of finding a particle in a closed volume is unity.
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Dept. of Physics
A function is said to be a normalisable wave function if it is
1. Single valued
2. Continuous
3. Finite
Application of Schrödinger’s equation:
Particle in an infinite potential well problem:
Consider a particle of mass m moving along X-axis in the region from X=0 to X=a in a one
dimensional potential well as shown in the diagram. The potential energy is zero inside the region
and infinite outside the region.
Applying, Schrodingers equation for region (1) as particle is supposed to be present in region (1)
But
The general solution to this expression is given by
At x=0,
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X = 0 X = a
Region (1)
V =0
V
Region (2)
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Dept. of Physics
At x=a, D sin ka = 0 ka = n where n = 1, 2 3…
E =
To evaluate the constant D: Normalisation : For one dimension
But
0 =1
D =
Eigen function: It is the physically acceptable solution to Schrodinger’s equation. It represents
the matter wave corresponding to a quantum particle in a specific state.
Ex: For a particle in an infinite potential well, the eigen function is
Eigen Value:It represents the energy of a particle in corresponding to its Eigen function.
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Dept. of Physics
Eigen value for a particle in an infinite potential well is E =
Assignments:
1. Study the applications of De broglies theory with regard to electron microscopes.
2. Heisenberg’s theory and Bohr’s theory are contradictory. Comment.
3. How do you relate the Newtonian Mechanics and Schrödinger’s Wave mechanics?
4. Wave nature and Particle nature are the properties of our interaction with light.
Explain.
5. Shape of S orbital is said to be spherical. Understand this through probability concept.
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Contents
CHAPTER 2: CRYSTAL PHYSICS
Basic definitions:
Crystal : It is that form of an object having regular arrangement of atoms.
Lattice point : These are the points in a crystal at which atoms are located.
Bravais lattice: It is a lattice with identical atoms at all the lattice points.
Space lattice : It is the regular three dimensional arrangement of atoms in a crystal.
Unit cell : It is the smallest portion of a space lattice which can generate the
complete crystal when repeated along the three perpendicular directions.
Crystal Lattice:
In a crystal, there is a regular arrangement of atoms. It is convenient to imagine three dimensional
array of points in space about which these atoms are located. Such points are known as lattice
points and the totality of such points forms the pace lattice. If all the lattice atoms are identical,
the lattice is called a Bravias lattice. Bravais showed that total number of different space lattices
with each atom having identical environment is only fourteen.
For the above mentioned two dimensional Lattice
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where are the fundamental translation vectors ,n1 and n2 are integers.
Basis: Every lattice point could be associated with on or more atoms known as basis which when
repeated in all directions, gives the crystal structure.
Unit cell: It is convenient to describe the crystal structure by assuming the crystal to be a
combination of small repeating entities known as unit cells. A unit cell is chosen such that all the
atoms in the structure are generated by translations of the unit cell through integral distances.
A crystal may have many unit cells. Generally, a unit cell with highest symmetry will be selected.
A unit cell with all the atoms at the corners is known as primitive unit cell.
A unit cell can be completely described by three vectors (representing the length) and α, β,
γ (representing the angles between the vectors). These parameters constitute lattice parameters.
This is a cubic unit cell .The intercepts a,b,c formed along the axes X,Y,Z by the intersection of
the faces are called as lattice parameters .
are the interfacial angles.
Crystal systems:
To represent lattice atoms in a given material, the following seven coordinate systems are used.
1. Cubic 5. Triclinic
2. Tetragonal 6. Rhombhohedral
3. Orthorhombic 7. Hexagonal
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B
B
c
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4. Monoclinic
CUBIC :
TETRAGONAL:
ORTHORHOMBIC:
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a = b = c α = β = γ = 900
a = b ≠ c α = β = γ = 900
a ≠ b ≠ c α = β = γ = 900
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MONOCLINIC:
TRICLINIC :
RHOMBOHEDRAL:
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a ≠ b ≠ c α = γ = 900 ≠ β
a ≠ b ≠ c α ≠ β ≠ γ ≠900
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a ≠ b ≠ c α = γ = 900 ≠ β
Dept. of Physics
HEXAGONAL:
Bravais lattice systems:
Cubic:
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a = b = c α = β = γ ≠ 900
a = b ≠ c α = β = 900 , γ = 1200
Simple Body centered Face centered
a = b = c α = β = γ = 900
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Tetragonal:
Orthorhombic:
Monoclinic:
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Simple Body centered
a = b ≠ c α = β = γ = 900
Simple Base centered Body centered Face centered
a ≠ b ≠ c α = β = γ = 900
Simple Base centered
a ≠ b ≠ c α = γ = 900 ≠ β
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Triclinic:
Rhombhedral:
Hexagonal:
Coordination number:
It is the number of nearest equidistant neighboring atoms for any atom in the lattice.
Simple cubic structure:
It has got lattice points at all the corners. Coordination number is 6.
Number of atoms per unit cell is 1
Ex: Polonium
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a ≠ b ≠ c α ≠ β ≠ γ ≠900
a = b = c α = β = γ ≠ 900
a = b ≠ c α = β = 900 , γ = 1200
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Dept. of Physics
Body centered cubic lattice:
It has got lattice points at all the corners and one at the geometrical centre of the cube.
Coordination number is 8. Number of atoms per unit cell is 2.
Ex: Li, Na, K, Cr
Face centered cubic lattice:
It has lattice points at all the corners and also at the centre of all the faces. The Coordination
number is 12.
There are 4 atoms per unit cell = 4
Ex: Al, Pb, Ag, Ni
Hexagonal close packed:
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It has lattice points at each corner, one atom each at the centre of the hexagonal face and three
atoms within the body of the unit cell.
Coordination number =12
Number of atoms per unit cell = 6atoms.
Miller indices:
Miller introduced a system to represent a plane in a crystal .He defined a set of three numbers to
specify a plane in a crystal.
Procedure:
1. Determine the intercepts of the plane along the X,Y and Z axes.
2. Find the reciprocal of these numbers.
3. Find the least common denominator (l.c.d) and multiply each by this l.c.d.The resulting
integers are called Miller indices and denoted as (h,k,l).
Example: If the intercepts of a plane are given by 4, 1, 2 then take the reciprocal.
l,c,d = 4
Miller indices 1, 4, 2
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Dept. of Physics
Definition: Reciprocals of the intercepts made by the plane on crystallographic axis when
reduced to small numbers.
Expression for interplanar spacing in terms of Miller indices:
Let ABC be one of the parallel planes represented by the Miller indices [h,k,l].Let its intercepts
be x,y,z. Imagine another plane passing through the origin O .OD is the perpendicular from O to
the plane ABC and OP is the interplanar distance .Let the angle made by OP with X,Y and Z axis
be and respectively.
Now [h, k, l] = where a, b, c are constants.
[x,y,z] = …………..(1)
Also from figure d=x cos
cos , cos , cos
Squaring and adding after Substituting for x, y, z from (1)
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Normal to the plane ABC
Normal to the plane ABC
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d2
If a = b =c, then
Expression for space lattice constant ‘a’ for a cubic lattice:
Density of material = Total mass of molecules belonging to unit cell / Volume of the unit cell
Mass of each molecule = Molecular weight / NA
Let the number of molecules in a unit cell be n.
Total mass of each molecule =
Density =
a =
Structure of Nacl:
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It is a face centered cubic structure. Na+ ( ) and Cl- ( ) ions occupy alternate corners and face
centered positions. Each ion has 6 ions of other type as its nearest neighbors. So its coordination
number is 6. It consists of two interpenetrating FCC sublattices; one made up of sodium atoms
and the two sub lattices are displaced by The positions of four sodium atoms are (0 0 0),
, , , while those of the chlorine atoms are )2
1
2
1
2
1( ,(0 0 ),( 0 0 ),
(0 0) . Each ion has 6 ions of other type as its nearest neighbors .So its coordination
number is 6 .Its lattice constant is a = 5.63 Å
Structure of Cesium chloride:
Structure of Diamond:
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Cs+
Cl-
It is a cubic structure.Coordination number is 8 .
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Diamond structure consists of two inter penetrating face centered cubic lattices. Each carbon
atom is surrounded by 4 other carbon atoms situated at the corners of a regular tetrahedron.
The unit cell for this structure is an FCC with a basis made up of two carbon atoms associated
with each lattice site .The positions of two basis atoms are( 0 0 0 )and .Each atom is
surrounded by four nearest atoms which form a regular tetrahedron.
Structure of Zinc Sulphide:
Packing factor:
It is the ratio of total volume occupied by the atoms in the unit cell to the total volume of the unit
cell.
For simple cubic structure:
Number of atoms per unit cell = 1
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Zn
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Dept. of Physics
Volume of one atom =
Volume of the unit cell = a3
Here a = 2R,
Volume of the unit cell = 8R3
Packing factor =
For BCC structure:
BCC:
Number of atoms per unit cell = 2
Volume of two atoms = 2.
Volume of the unit cell = a3
For BCC, a =
Volume of the unit cell =
Packing factor = 0.68
For FCC structure:
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Dept. of Physics
Number of atoms per unit cell = 4
Volume occupied by four atoms = 4 X
For FCC, a =
Volume of the unit cell = a3 = 16 R3
Packing factor = (16/3) R3 / 16 R3 = 0.74
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Dept. of Physics
Assignments:
1. How do you relate the properties of crystals which you have studied in this chapter with
their applications ?
2. Study the different techniques used to determine the structure of a crystal.
3. How important is the study of crystal physics in understanding the DNA structure?
4. Discuss the techniques which were used by Watson and Crick to propose the double
Helix structure of DNA
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Dept. of Physics
Contents
Chapter 3: X-rays (Discovered by Roentgen in 1895,Wavelength range 10 Ǻ – 1 Å )
Production :
X-rays are produced when fast moving electrons are suddenly stopped by a solid target. Coolidge
tube is as shown in the figure. The pressure inside is 10 -5mm of Hg. The cathode is Tungsten
filament heated by a high tension battery. The electrons emitted by filament through thermoionic
emission are accelerated towards the target. The target must be cooled to remove the heat
generated.
Properties of X-rays:
1. They are not deflected by electric and magnetic fields.
2. They have no charge.
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Electron beam
X-rays
Target
Cooling plant
Coolidge tube apparatus
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Dept. of Physics
3. They cause fluorescence.
4. They have high penetrating power.
5. They affect photographic plates
X- Ray spectrum:
The graph of Intensity of X- rays against wavelength is as shown. The smoothly varying curves
represent the continuous spectrum. But as the applied voltage is increased sharp peaks are seen.
This feature is known as characteristic spectrum representing the characteristics of the target
atoms.
Features:
1. For each potential, there is a minimum wavelength.
2. As voltage is increased, λmin is shifted towards smaller values.
3. At lower voltages the graph is continuous. Continuous spectrum is formed due to the fact that
electromagnetic radiations are emitted in all frequencies when a charged particle is
accelerated.
4. Characterstic spectrum is due to the transition of electrons within the target atoms that have
been hit by electrons. Suppose an atom in the target is bombarded by a high speed
electron and K-shell electron is removed, a vacancy is created in K-shell. This vacancy is
filled up by an electron from L,M,N shells .These possible transitions result in the
lines.
Laue spots:
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Wavelength
30Kv
λmin
Intensity 70Kv
40Kv
Line spectrum or characteristic spectrum
Continuous spectrum
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Dept. of Physics
X- Rays were passed through a crystal (like ZnS).The transmitted light was received on a
photographic plate. After exposure the photographic plate looked as shown in the figure. The
central dark spot arises due to direct beam. The central spot is surrounded by many fainter spots
arranged in a definite pattern .This indicates that the incident X-ray beam has been diffracted
from the various crystal planes .These spots are called as Laue’s spots.
Bragg’s law:
Let us consider a set of parallel lattice planes of a crystal separated by a distance ‘d’.Suppose a
narrow beam of X-rays of wavelength λ is incident upon these planes at an angle θ as shown in
the figure.
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Coolidge tube
slitsZnS crystal
X-ray beam
Photographic plate
Atomic planes
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Developed photographic plate
Dept. of Physics
Consider the ray PQ incident on the first plane. It is reflected along QR .The rays P1Q1and Q1R1
are the incident and reflected rays. QT and QS are the normals.
Total path difference between the two rays = T Q1 + Q1S = 2d sinθ
From triangles Q T Q1 ,
Q Q1 S Q1 S = d sinθ
If the path difference is nλ, then constructive interference takes place and maximum
intensity is produced.
2d sinθ =nλ
X-ray diffraction spectrometer : Apparatus: A source of X-ray, slits, crystal mounted on a circular turn table spectrometer with
vernier scale.
Construction: X –ray beam after reflection from the crystal enters the ionization chamber
mounted on a mechanical arm which can turn co axially with the turn table .This ionization
chamber is coupled with the turn table so that if the turn table rotates through an angle ‘θ’, the
ionization chamber rotates through ‘2θ’.The ionization current produced by X-rays is recorded by
the electrometer.
Working: The ionization current is measured for different values of glancing angle ‘θ’. A plot is
then obtained between ‘θ’ and ionization current .For certain values of ‘θ’, the intensity of
Ionization current increases abruptly.
Whenever the crystal receives X-rays at an angle of incidence satisfying Bragg’s law
2d sinθ = nλ ,constructive interference takes place and maximum intensity occurs .The rise in
current occurs more than once as ‘θ’ is varied because the law is satisfied for various values of ‘n’
i.e., 2d sin θ = 1λ ,2λ,3λ etc.
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Dept. of Physics
Application of X-rays :
1. To detect cracks and cavities in different structures.
2. Used to study the structure of alloys.
3. To detect homogeneity of welded points.
4. To study the structure of solids and organic molecules.
5. To study bone structures.
6. To treat cancer.
7. To study the structure of genes.
Moseley’s law:
According to this law, the frequency of a spectral line in x-ray spectra varies as the square of
atomic number of the element emitting it.
- Frequency
Z - Atomic number
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Coolidge tube (Source of X-ray)
slit
Electrometer
Turn table on which powdered crystal is taken
Vernier scale
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Dept. of Physics
Applications:
1. From this law it was understood that it is the atomic number which determines the physical
and chemical properties of elements.
2. The discrepancy in the position of certain elements like Argon and Potassium:
i.e., should come before
3. It helps in predicting the existence of undiscovered elements.
Assignments:
1. Study the application of X – ray diffraction technique in the field of Bio technology.
2. Collect information about CHANDRA X- RAY SPACE TELESCOPE launched few
years back by NASA.
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Dept. of Physics
Contents
CHAPTER 4: Electron conduction in solids:
Classical free electron theory:(Drude – Lorentz theory)
Postulates:
1. A metal is assumed to possess a three dimensional array of ions in between which there
are freely moving valence electrons confined to the metallic boundary.
2. These free electrons are treated as equivalent to gas molecules and they are assumed to
obey the laws of kinetic energy of gases. In the absence of any electric field the energy
associated with electrons is equal to
Kinetic energy =
3. The electric current in a metal is due to the drift of electrons in a direction opposite to
Electric field.
4. The electric field due to all the ions is assumed to be constant.
Drift velocity:
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Dept. of Physics
The net displacement in the position of electrons per unit time caused by the application of
electric field is known as drift velocity.
Explanation:
Consider a cylindrical metal connected to a voltage source. The free electrons experience a force F = qE
From Newton’s second law F = ma = m
If u = 0 , v = vd , t = then
qE = m
vd =
Where e – charge on the electron, E – Electric intensity, - Mean collision time.
Mean Collision Time: It is the average time taken between two consecutive collisions of
electrons.
Relaxation time: It is the time taken for the drift velocity to decay to (1/e) times after the
removal of electric field.
Mean free path: The average distance traveled by the electrons between two successive
collisions.
Expression for the electric current through a metal :
Consider a cylindrical conductor with area of cross section A , electron concentration ‘n’
connected to a voltage source. Let the drift velocity be Vd.
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Dept. of Physics
The number of electrons crossing unit area of a imaginary cylinder of length vd per second
is given by n A vd
Total charge crossing unit area per second = neAVd
By definition Electric current =
Electric current = neAVd
Expression for electrical conductivity :
Step 1: Derive the expression for Vd.
Step 2: Derive the expression for Electric Current.
Step 3 : From the definition of current density J =
From Ohms law J = E
=
Variation of resistivity with temperature:
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V
T
For metals
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Dept. of Physics
Matthisen’s rule: It states that the total resistivity of a metal is due to the sum of resistivity due
to scattering of electrons with lattice vibrations which is temperature dependent and resistivity
due to the scattering of electrons by impurity atoms/ defects which is temperature independent.
=
Note:
1. Thermal conductivity: K =
2. Electrical conductivity:
3. Widemann Franz law: The ratio of the thermal conductivity to the electrical conductivity of
metals is proportional to the absolute temperature.
Mobility of electrons:
It is defined as the ratio of the drift velocity to the electric field applied.
It can be shown that .
Failures of Classical free electron theory:
1. Prediction of low specific heats for metals:
Classical free electron theory assumes that conduction electrons are classical particles similar to
gas molecules. Hence,they are free to absorb energy in a continuous manner. Hence metals
possessing more electrons must have higher heat content. This resulted in high specific heat given
by the expression CV = .
This was contradicted by experimental results which showed low specific heat for metals.
2. Temperature dependence of electrical conductivity:
From the assumption of kinetic theory of gases
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Dept. of Physics
Also mean collision time τ is inversely proportional to velocity,
However experimental studies show that
3. Dependence of electrical conductivity on electron concentration:
As per free electron theory,
The electrical conductivity of Zinc and Cadmium are 1.09 x 107 /ohm m and .15 x 107 /ohm m
respectively which are very much less than that for Copper and Silver for which the values are
5.88x107 /ohm m and 6.2 x 107 /ohm m. On the contrary, the electron concentration for zinc and
cadmium are 13.1x1028 /m3 and 9.28 x1028 /m3 which are much higher than that for Copper and
Silver which are 8.45x1028 /m3 and 5.85 x1028 /m3.
These examples indicate that does not hold good.
4. Mean free path, mean collision time found from classical theory are incorrect.
Quantum free electron theory:
Assumptions:
1. The energy of conduction electrons in a metal is quantized.
2. The distribution of electrons amongst various energy levels is according to Pauli’s exclusion
principle and Fermi – Dirac statistical theory.
3. The average kinetic energy of an electron is equal to
4. The attraction between the electrons and ions, the repulsion between electrons are ignored.
Fermi – Dirac theory:
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Dept. of Physics
According to this theory, the free electrons are quantum particles .The distribution of electrons
amongst various energy levels is according to Pauli’s exclusion principle. the number of
conduction electrons per unit energy range per unit volume is given by
n(E)de = g(E)dE . f (E)
where g (E) is density of states
f(E) is the Fermi probability factor .
Fermi energy ( ):
It is the highest energy possessed by an electron at zero Kelvin.
Fermi probability factor: It represents the probability of occupation of an energy level.
f (E) =
Density of energy of states:
It represents the number of energy levels per unit energy range per unit volume.
g (E)=
To show that energy levels below Fermi energy are completely occupied:
For E < EF, at T = 0,
f (E) = =
To show that energy levels above Fermi energy are empty:
For E > , at T=0
f (E) = =
At ordinary temperatures, for E = EF,
f(E) =
Fermi energy for T > 0k, Ef = Ef0
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Dept. of Physics
Success of quantum theory:
1. Specific heat:
Classical theory predicted high values of specific heat for metals on the basis of the assumption
that all the conduction electrons are capable of absorbing the heat energy as per Maxwell -
Boltzmann distribution i.e., CV=
But according to the quantum theory, only those electrons occupying energy levels close to
Fermi energy (EF ) are capable of absorbing heat energy to get excited to higher energy levels.
Thus only a small percentage of electrons are capable of receiving the thermal energy and specific
heat value becomes small.
It can be shown that CV = .
This is in conformity with the experimental values.
2. Temperature dependence of electrical conductivity.
According to classical free electron theory,
Electrical conductivity
Where as from quantum theory
Electrical conductivity
This is in agreement with experimental values.
3. Dependence of electrical conductivity on electron concentration:
According to classical theory,
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T= 0 K
T> 0 K
EF
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Dept. of Physics
But it has been experimentally found that Zinc which is having higher electron concentration
than copper has lower Electrical conductivity.
According to quantum free electron theory,
Electrical conductivity where VF is the Fermi velocity.
Zinc possesses lesser conductivity because it has higher Fermi velocity.
Application of Quantum free electron theory :
Thermionic emission:
It is the process of emission of electrons from the surface of metallic conductors on heating to
high temperature.
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EF
Φ
Fermi level
Highest energy level beyond which electrons are free
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Dept. of Physics
At T = 0K all the levels up to the Fermi level are filled. As the temperature is increased, the
electrons are excited thermally and move to higher energy states. For the electrons to be ionized,
they must acquire a minimum energy known as work function.
The current density J = AT2 where
A – Emission constant ,T– Temperature, Φ – work function, K – Boltzmann constant.
Density of states:
It is defined as the number of energy levels per unit energy range per unit volume.
To determine the density of states, we first count the number of states that have energy below this
energy level. This is done using the diagram given below in quantum number space.
The lattice consists of points with positive integer coordinates (n1,n2,n3) and occupies one octant
of three dimensional space .Each point corresponds to one energy level for a particular value of
n1,n2,n3 such that it is the square of the distance of the point from the origin.
So for a 3 dimensional cube of a length L
E = ……………………(1)
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n1
n2
n3
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Dept. of Physics
Therefore all lattice points within the octant of radius R correspond to energy, less than or equal
to E .If each cubic cell in the figure is of unit volume , and one point (one energy level)
corresponds to each cubic cell , then the total number of points in the octant of radius R is equal
to the volume of the octant.
Total number of energy levels less than energy E = Total number of points or total number of
cells
= volume of the octant
=
Since each level can accomodate two electrons of opposite spin
Total number of energy levels less than energy E is N =
Substituting for R
N =
Density of states g(E) = Number of energy levels of energy E in the range
E = dN/dE =
g(E)(dE) = dE
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Dept. of Physics
Assignments:
1. Study the applications of quantum theory to understand the properties of metals.
2. The density of states is a universal constant. Explain.
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Dept. of Physics
ContentsCHAPTER 5: Magnetic materials :
Diamagnetism:
Langevein’s theory:
The atoms of the diamagnetic material do not possess magnetic moment .They have completely
filled shells. Diamagnetism is the result of Lenz’s law operating in atomic scale.
When a diamagnetic material is kept in a magnetic field, the magnetic flux through the surfaces
bounded by the molecular circulatory currents is increased and a current is induced in each
elementary circuit as to oppose the external field. This reduces the density of flux lines. Hence
diamagnetic materials get repelled by the magnetic field.
They are characterized by negative susceptibility, magnetic permeability less than one.
Ex: Cu, Au, Ge, diamond, Nacl, Al2O3
The magnetic moment induced by the external field B is given by
The negative sign shows that the induced moment is opposite to the applied field.
According to Langevein theory, diamagnetism is attributed to the influence of the magnetic field
on the orbital momentum of the electrons.
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Dept. of Physics
Diamagnetic susceptibility = χ =
Paramagnetic materials:
Paramagnetism occurs in materials where the atoms or molecules possess a feeble magnetic
moment.
The orbital and spin motion of electrons contributes to that.
Langevin’s Theory of Paramagnetic materials:
When a paramagnetic material is kept in a magnetic field, atoms with individual magnetic
moments tend to align in the direction of magnetic field and the specimen acquires magnetization
in the direction of magnetic field.
Characteristics:
1. Low magnetization, low susceptibility.
2. Susceptibility is small, positive and varies inversely with temperature.
3. Permeability is greater than 1.
Paramagnetic susceptibility χ =
Where C is curie constant .
This result namely the magnetic susceptibility of atoms varies as is known as Curies law.
Ex: CuSO4 , O2
Paramagnetic susceptibility = χ =
Weiss theory of Paramagnetism:
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Absence of magnetic field Presence of magnetic field
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Dept. of Physics
Langevin theory failed to explain the complex relation between susceptibility and temperature
exhibited by paramagnetic substances. Also this theory does not explain the relationship between
para and ferromagnetism.
Weiss introduced the concept of internal molecular field in order to explain the dependence of
susceptibility. In a gas, the molecules are influenced by their magnetic moments and
consequently, there should exist a field with which they interact.
Weiss derived the expression for susceptibility as
Paramagnetic susceptibility = χ =
Here θc is known as Curie point.
This result is in agreement with the experimental results.
Ferromagnetism:
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.
Ex: Fe, Ni,gd,Dy
According to Weiss law, the resultant field in a ferromagnetic material is the sum pf applied field
and field due to all the magnetic dipoles .
where γ is Weiss molecular constant.
Ferromagnetic susceptibility χ =
B – H graph in Ferromagnetic materials
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Dept. of Physics
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.
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BsatBr
-Hc
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Dept. of Physics
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.
Ceramic magnets:
These are the magnetic materials with metallic and non metallic elements. They possess
ferromagnetic properties like domain structure, hysteresis curve etc.
They are expressed by the general formula MO Fe2 O3 .They possess strong ferromagnetic
properties such as domain structure, hystresis.
Properties: 1.High magnetic permeability
2. High electrical resistance
3. High remnant magnetism, Coercivity
Ex: Ferrites – Manganese ferrite, Nickel Ferrite
Applications:
1. Hard ferrites are used in the production of permanent magnets.
2. Soft ferrites are used to make cores of transformers.
3. They are used in magnetic films, magnetic discs, magnetic tapes.
Soft magnetic materials:
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Dept. of Physics
These are temporary magnets which can retain magnetism for a short interval of time. They
possess small hysteresis loss.
Properties:
- Low remnant magnetism
- High permeability
- High susceptibility
Ex: Soft iron, Si, Steel, Alloys
Uses: They are used in the construction of cores of transformers.
Hard magnetic materials :
These are the magnetic materials which can retain magnetism permanently.
They possess large hysteresis loop, large remnant magnetization, and high coercivity.
Ex: Carbon, tungsten.
Uses: They are used in making permanent magnets, microphones, loud speakers.
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Dept. of Physics
Assignment:
1. List out the importance of magnetic materials in electronic circuits.
2. An atom is a magnet. Comment.
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Dept. of Physics
Contents
CHAPTER 6: SUPER CONDUCTIVITY :[KAMERLINGH IN 1914]
It is a phenomenon in which some materials loose their resistance completely below certain
temperature.
Temperature dependence of resistivity:
Critical temperature: (TC)
It is the temperature at which a normal material transforms to superconducting state.
Material TC (K)
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T
For metals
T
For superconductors
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Dept. of Physics
HgBa2 Ca2Cu3O8 134
Bi-Sr-Ca-Cu-O 105
YBa2Cu3O7 92
Nb3Ge 23.2
Nb 9.46
Pb 7.18
Hg 4.19
Zn 0.88
BCS Theory :[Bardeen , Cooper, Schrieffer]
According to this theory superconductivity occurs when an attractive interaction known as
electron-lattice-electron interaction is established resulting in the formation of cooper pairs.
In a lattice, an electron passing close to a lattice atom is attracted towards it and displaces it. This
lattice atom will interact with another electron and in turn forms an electron – lattice –
interaction. This system of two electrons of equal and opposite momentum attached to a lattice
atom is known as a cooper pair. The electrons are bound to the lattice atom through the exchange
of phonons (Lattice vibrations).When electrons flow in the form of cooper pairs they do not get
scattered as the energy required to break it up is large enough. This reduces the resistance.
Properties of superconductors:
1. When a superconductor is placed in a magnetic field, it expels the magnetic flux out of its body
and behaves like a diamagnet.This effect is known as Meisseners effect.
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Lattice atom
ElectronElectron
Phonons
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Dept. of Physics
2. They have abnormal specific heats.
3. Isotope effect:
Isotopes of an element possess different critical temperatures.
The critical temperature is inversely proportional to the isotopic mass.
where
Ex: for is 4.185K
For is 4.16K
Types of superconductors
Type 1 Superconductor:
These are pure superconductors.
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SuperConductor
Normal state
Superconducting state
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Dept. of Physics
When kept in magnetic field, initially they continue to exhibit superconductivity and the negative
magnetic moment increases. At critical magnetic field there is a sharp transition to normal
state .These possess low critical magnetic fields.
Ex: Al,Pb
Type 2 superconductor:
These are generally alloys.
When kept in magnetic field, initially they continue to exhibit superconductivity and the negative
magnetic moment increases. At HC1, the flux lines start penetrating .As the magnetic field is
increased, the super conductivity coexists with magnetic field and this phase is known as mixed
state(vortex state). At higher critical magnetic field HC2, the penetration is complete and the
material transforms to normal state.
Ex: Nb3Ge, YBaCu2O3
Applications of superconductivity:
1. Super conducting magnets:
Superconducting magnets are used to develop strong magnetic fields required in various
techniques such as MRI scanning, detection of ore deposits etc.
A superconducting solenoid consists of superconducting filaments embedded in copper matrix.
The matrix prevents mechanical fractures that may happen in the superconducting material due to
the flow of large currents.
High field magnetic applications
Nuclear magnetic resonance (medical diagnostics)
Magnetic levitation
Ore refining
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Superconducting state
Vortex state
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Dept. of Physics
Magnetic shielding
2. Maglev vehicles:
These are the vehicles which are set afloat above the track reducing the friction. With such an
arrangement, great speeds could be achieved with low energy consumption.
The vehicle consists of superconducting magnets built at the base. Large currents are passed
through aluminum guide way. Due to the interaction between the magnetic fields produced by the
superconducting magnet and the aluminum guide way, the vehicle is set afloat. These magnetic
fields also propel the vehicle.
3. Lossless power transmission:
Since there is no resistance to the flow of current in a superconductor, they can transfer electrical
power without any loss. In ordinary conductors, 30-40% of the power is lost on account of Joules
heating effect.
DC Josphsons effect:
When the distance between the two superconducting bars is reduced below 1nm, the voltmeter
suddenly due to the passage of electric current in the energy gap.
AC Josephsons effect:
When the superconducting bars are insulators, on application of a voltage between the
superconducting bars, a high frequency electromagnetic radiation emanates from the gap.