21PHY12-Questions & Answers
21PHY12-Questions & Answers
Module-1 : Syllabus
1.1Free Oscillations: Definition of SHM, Characteristics; Examples and Derivation of No numerical
𝒅𝟐 𝒚 𝒌 problems
+ y = 𝟎 differential equation of motion for SHM starting from Hooke’s law.
𝒅𝒕𝟐 𝒎
Mechanical simple harmonic oscillator: Mass suspended to spring (vertical vibrations) - Numerical
Description, Mention of Expression for time period/frequency, Definition problems
of force constant and its significance, Derivation of expressions for force constants for
𝒌 .𝒌
series (𝒌𝑺 = 𝟏 𝟐 ) and parallel combination of springs (𝒌𝑷 = 𝒌𝟏 + 𝒌𝟐 )
𝒌𝟏 + 𝒌𝟐
Definition of free oscillations with examples, mention the equation of motion, Natural Numerical
frequency of vibration - Qualitative discussion. problems
1:2 Damped oscillations: Definition with examples. Derivation of decaying amplitude, Numerical
Discussion of 3 .cases viz, over damping, critical damping ,under damping. problems
Quality factor-Definition, equation and its significance,
1.3 Forced oscillations: Definition with examples. Derivation of expressions for Numerical
amplitude and phase of forced vibrations. problems
Discussion of 3 cases (i) p≪w, (ii) p= w and iii) p» w
Resonance: Definition, Examples, Condition for resonance and expression for maximum
amplitude (just mention) and Sharpness of Resonance: Definition and significance,I
I mention the effect of damping on sharpness of resonance
Module-1
𝒅𝟐 𝒚 𝒌
1. Derivation of differential equation of motion for SHM from Hook’s law 𝟐 + 𝒚 = 𝟎
𝒅𝒕 𝒎
2. Derivation of expressions for force constants for series and parallel combination of springs.
𝒌 𝒌
𝒌𝑺 = 𝟏 𝟐 and 𝒌𝑷 = 𝒌𝟏 + 𝒌𝟐
𝒌𝟏 +𝒌𝟐
3. Definition of control volume and Law of conservation of mass, energy and momentum (Statements
with equations)
4. Reddy shock tube- construction ,Working and its applications
5. Derivation of expression for decaying amplitude and phase of forced vibrations and discussion
following 3 cases :
i) p≪ 𝝎 ii) p= 𝝎 iii) p≫ 𝝎
6. Definition of Mach number and classification of Subsonic, Supersonic, Transonic and Hypersonic
waves based on Mach number.
7. Definition of Shock waves and their properties and uses.
8. Derivation of decaying amplitude and discussion of 3 cases namely Over damping, Critical damping
and Under damping.
OSCILLATIONS
Oscillations are periodic motions. If the oscillations occur without the action of an external
periodic force then such oscillations are called free oscillations. The motion of an object is
said to be SHM, if the restoring force (or acceleration) is directly proportional to the
displacement and acts in the direction opposite to that of motion.
O
C• • • •D
A x
A
Equilibrium position
Examples of SHM :
1. A mass suspended to a spring when pulled down and left free executes SHM
vertically.
2. A pendulum set for oscillations.
Harmonic Oscillations: Any motion, which repeats itself at regular intervals is called
Harmonic Oscillations. The oscillatory motion in which the force acting on the body is
directly proportional to the negative of the displacement is called SHM.
𝒅𝟐 𝒚 𝒌
Differential equation of motion for SHM + 𝒎 𝒚 = 𝟎 from Hook’s law and mention of its
𝒅𝒕𝟐
solution .
F = −𝑘 𝑦 F = −𝑘 𝑦
F=0
F
m
Type equation here.
y
m Equilibrium position
y
Let a mass ‘m’ suspended by a spring of spring constant ‘ k ’ rests about its equilibrium
position as shown in the diagram.
Pull the mass through a distance ‘ y ‘ and release. The mass execute SHM about the
equilibrium position. Then the restoring force acting on the body due to elongation
/contraction is given by Hook’s law as
F = − k y …(1)
𝑤ℎ𝑒𝑟𝑒 − 𝑣𝑒 𝑠𝑖𝑔𝑛 indicate that force and displacement are opposite to each other.
According to Newton’s 2nd law the restoring force (inertial force) produce an
acceleration ‘ a ‘ given by F = 𝒎𝒂 ….(2)
𝑑2 𝑦
∴ from eqns 1 & 2 ,we get 𝑚𝑎 = − k y , but a = 𝑑𝑡 2
𝑑2 𝑦
∴ 𝑚 𝑑𝑡 2 = − k x
𝑑2 𝑦 𝑘
= −𝑚 y
𝑑𝑡 2
𝒅𝟐 𝒚 𝒌
+ 𝒎 y = 𝟎 ….(3)
𝒅𝒕𝟐
this eqn is called differential equation of Simple Harmonic Motion.
The solution of equation 3 is y = a sin(𝝎𝒕) …..(4), where A is amplitude , 𝜔𝑡 is
phase at time t. 𝝎 is also called the natural frequency of vibration.
Differentiate equation (4) w.r.t ‘t’
𝑑𝑦
= a 𝜔 cos 𝜔𝑡
𝑑𝑥
𝑲
𝝎= √
𝒎
2𝜋 𝑚
Note: 1. The time period of oscillation is given by T = = 2𝜋√ 𝑘
𝜔
Mechanical SHM: (Mass suspended to a spring):
Rigid support Consider a spring whose one end is fixed to rigid support.
Let a mass m be attached to its lower end due to which a
Load mg acts on the spring vertically downwards. The
Equilibrium level of the spring with the load is at O.
Any displacement upwards from O taken positive and below
is considered as negative. Suppose the mass m is pulled down
m B within the elastic limit by a distance –y. Let the force required to
do it be –F. Then the upwards restoring generated within the
-y O spring will be +F. since by Hooke’s law,
restoring force α - displacement
A -ve sign indicates that the restoring force acts in a direction
m
Opposite to the displacement.
W = mg F α –y
F = - ky Where K- force constant/ stiffness factor.
|−𝑭| 𝑭
k= ≈ for y=1,K=F thus , the force constant is defined as “ It is the magnitude of the
𝒚 𝑿
applied force that produces unit extension(or compression) in the spring while it is loaded
within the elastic limit”.
Significance:
1. K is a measure of stiffness.
2. In the case of springs, It represents how much force it takes to stretch the spring
over a unit length. Thus, springs with larger values for force constant will be stiffer,
It is also called Spring constant.
amplitude.
2. Frequency (ν) is the number of oscillations per second and is the reciprocal of
period.
𝟏 1 𝐾 2𝜋
𝝂 = 𝑻 or 𝝂 = 2𝜋 √𝑚 ……………..Hz and angular frequency is given by,𝜔 = 𝑇
𝑲
∴ 𝝎 = √ …………..radian/second
𝒎
𝐹1 𝐹2 F
𝑘1 𝑘2 𝑘𝑝
m
y y
m m
Consider two springs of constants 𝒌𝟏 𝒂𝒏𝒅 𝒌𝟐 are suspended in parallel with a load ‘m’
Let the mass is pulled through a distance ‘x’ and released. The mass execute Up And Down
motions. Let 𝑭𝟏 𝒂𝒏𝒅 𝑭𝟐 be the restoring forces that act in the springs of constants
𝒌𝟏 𝒂𝒏𝒅 𝒌𝟐 respectively. Then 𝑭𝟏 = −𝒌𝟏 𝒚 𝒂𝒏𝒅 𝑭𝟐 = −𝒌𝟐 𝒚
and net restoring force acting on mass, F = 𝑭𝟏 + 𝑭𝟐 = −(𝒌𝟏 + 𝒌𝟐 )𝒚 ….(1)
also if 𝒌𝑷 be the spring constant of the system of springs in parallel ,then F = = −𝒌𝒚 …(2)
𝑚
From Eqns 1&2 ,we get , 𝒌𝑷 = 𝒌𝟏 + 𝒌𝟐 and T = 2𝜋√𝐾
𝑝
Note:
Let 𝑭𝟏 𝒂𝒏𝒅 𝑭𝟐 be the restoring forces that act in the springs of constants 𝒌𝟏 𝒂𝒏𝒅 𝒌𝟐
𝑭
respectively. Then 𝑭𝟏 = −𝒌𝟏 𝒚𝟏 or 𝒚𝟏 = − 𝒌𝟏 ……(2)
𝟏
𝑭
𝑭2 = −𝒌2 𝒚𝟐 or 𝒚2 = − 𝒌2 …….(3)
𝟐
𝐹1
𝒌𝟏 F
𝐹2 𝑦1 𝑘𝑆
𝑘2
𝑦2 m
m
y
y
m
Also if 𝒌𝑺 be the spring constant of series combination and F the net restoring force acting
𝑭
on the mass ,then F= −𝒌𝑺 𝒚 or 𝒚 = − 𝒌 …. (4)
𝑺
𝑭 𝑭 𝑭
∴ From eqns 1,2,3&4,we get, = 𝒌𝟏 + 𝒌2
𝒌𝑺 𝟏 𝟐
𝟏 𝟏 𝟏 𝒌𝟏 .𝒌𝟐 𝑚
Then = + or 𝒌𝑺 = and T = 2𝜋√
𝒌𝑺 𝒌𝟏 𝒌𝟐 𝒌𝟏 + 𝒌𝟐 𝐾𝑠
Over damping
Displacement
Critical damping
Under damping
time
Quality factor (Q- factor): “It is defined as the number of cycles required for the energy to
fall off by a factor of 𝒆𝟐𝝅 (≅ 535)”.
The energy loss rate of a weakly damped harmonic oscillator is characterizes in terms of a
parameter Q , which is known as quality factor. Or To describe the amount of damping with
a quantity called Quality factor.
𝑾
Q= it is a unit less quantity.
𝟐𝒃
𝑤
2b = sub in equation given below
𝑄
𝒅𝟐 𝒙 𝒘 𝒅𝒙
∴ + 𝑸 𝒅𝒕 + 𝝎𝟐 𝒙 = 𝟎
𝒅𝒕𝟐
Significance of Q- factor: It is defined as the number of cycles required for the energy to fall
off by a factor of 𝒆𝟐𝝅 (≅ 535). Larger number of cycles gives larger values for Q which
means, the sustenance of oscillations is more thereby overcoming the resistive forces.
Thus, Q-factor describes how much under damped is the oscillating system.
Forced oscillations(Vibrations) : These are the oscillations executed by the body with the
frequency of the external periodic force with constant amplitude, but not with its natural
frequency.
Consider a body of mass m displaced through a distance x at any instant of time t ,when an
external periodic force F Sin(pt) of angular frequency p acts on it opposite to its direction.
𝑑𝑥
Then the damping force acting on the body opposite to the its direction (p)is −𝑟 𝑑𝑡 ,where r
is damping constant.
Also the restoring force acting on the body is – 𝑘𝑥 , where k is force constant.
𝑑𝑥
∴ The net resultant restoring force acting on the body = −𝑟 𝑑𝑡 – 𝑘𝑥 + F Sin(pt) ……(1)
𝑑2𝑥
According to Newton’s 2nd law, the resultant force on the body = m ….(2)
𝑑𝑡 2
𝑑2𝑥 𝑑𝑥
From eqn 1&2 ,we get, m = −𝑟 𝑑𝑡 – 𝑘𝑥 + F Sin(pt)
𝑑𝑡 2
𝑑2𝑥 𝑑𝑥
∴ m +𝑟 + 𝑘𝑥 = F Sin(pt) This is eqn of forced vibration motion
𝑑𝑡 2 𝑑𝑡
𝑑2𝑥 𝑟 𝑑𝑥 𝑘 𝐹
On re-arranging ,we get , + 𝑚 𝑑𝑡 + 𝑚 𝑥 = 𝑚 Sin(pt) …(3)
𝑑𝑡 2
𝑟 𝑘 𝑘
Let = 2𝑏 & WKT 𝜔2 = 𝑚 ∵ 𝜔 = √𝑚
𝑚
𝑑2𝑥 𝑑𝑥 𝐹
∴ +2𝑏 𝑑𝑡 + 𝜔2 𝑥 = 𝑚 Sin(pt)……………(A)
𝑑𝑡 2
The solution of this differential equation is x = 𝑎 𝑆𝑖𝑛(𝑝𝑡 − 𝛼) ……(4)
Where a and 𝛼 represent amplitude and phase of the vibrating body.
Resonance : Resonance is the frequency with which the body oscillates when the natural
frequency of the body is equal to the frequency of the external periodic force acting on the
body.
At resonance the energy transfer from external periodic force is maximum and the
amplitude is also maximum.
Ex:
1. Helmholtz resonator.
2. A radio receiver set tuned to the broadcast frequency of a transmitting station.
3. The vibrations caused by an excited tuning fork in an other nearby identical tuning
fork.
Conditions for resonance:
1. The frequency of the applied force (p) must be equal to the natural frequency(𝜔) of
oscillations of the body.
𝑟
2. b = must be minimum or Damping caused by the medium must be minimum.
2𝑚
𝐹/𝑚
At resonance the amplitude is given by 𝑎𝑚𝑎𝑥 = ∵ p= 𝜔
2𝑏𝜔
𝐹/𝑚
The amplitude of the body near resonance a = the state of vibration under this
2𝑏𝑝
condition is known as Resonance.
Sharpness of Resonance:
The process of varying the frequency of the applied force to match the resonance frequency
of a vibrating body is called “tuning”.
I/II SEM Page 12
RAMESH R 21PHY12/22
Sharpness of resonance is the rate at which the amplitude changes corresponding
to a small change in the frequency of the applied external force, at the stage of resonance.
𝐹
𝐶ℎ𝑎𝑛𝑔𝑒 𝑖𝑛 𝑎𝑚𝑝𝑙𝑖𝑡𝑢𝑑𝑒 𝑎𝑚𝑎𝑥 −𝑎 ( )
𝑚
i.e, Sharpness of resonance = = =
𝑐ℎ𝑎𝑛𝑔𝑒 𝑖𝑛 𝑓𝑟𝑒𝑞𝑢𝑒𝑛𝑐𝑦 𝑝−𝜔 2𝑏𝜔𝑝
Undamped( b=1)
a
Heavily damped(b=3)
The variation of amplitude of forced oscillations with respect to damping is as shown in the
graph .
From the graph it is clear that the maximum amplitude at resonance is a function of
damping. Higher the damping lower will be the amplitude at [Link] the
sharpness will be higher at lower damping and vice-versa is the significance.
Significance of Sharpness of resonance:
The amplitude of oscillations of an oscillating body or system rises to a maximum when
the frequency of the external periodic force matches with the natural frequency of the
oscillating system. However , the rise of the amplitude will be very sharp when the
damping is very small.
SHOCK WAVES
Q: Define Mach number, subsonic waves supersonic waves and Mach angle (Classification
of
objects based on Mach number)
1. Mach Number(M) is the ratio of the speed of an object (V) through a fluid to the speed of
𝑽
sound(a) in the fluid at that point and is given by M =
𝒂
2. Subsonic waves are the mechanical waves whose speed is less than that of sound in the
same medium. Mach number of Subsonic waves is less than 1.
Ex: Motor cycle, Bus, Train , aero planes etc produce subsonic waves.
3. Supersonic waves are the mechanical waves whose speed is greater than that of sound in
the same medium. for which the Mach number of Supersonic waves is greater than 1.
Ex: Fighter planes, Rockets, Missiles, tornado etc produce supersonic waves
4. Mach angle(𝝁) is the half the angle of cone of sound waves formed and is given by
𝟏
𝝁 = 𝑺𝒊𝒏−𝟏 ( )
𝑴
Classification of types of fluid flow
0 < 𝑀 < 0.3 03 < 𝑀 < 0.8 0. 8 < 𝑀 < 1.2 1.2 < 𝑀 < 5 5<𝑀
0 0.3 0.8 1.2 5
Q: Control Volume.
Control volume is a model on the basis of which the shock waves are analyzed. It is an
thin envelope that surrounds the shock front within which, there is a sharp increase in the
pressure, temperature and density in the compressed medium.
Pressure, Volume, density and temperature changes within the control volume are large
𝑃1 𝑃2
𝑉1 𝑉2
𝜌1 𝜌2
ℎ1 ℎ2
𝑚1 𝑚2
𝑝𝑟𝑒 𝑠ℎ𝑜𝑐𝑘 𝑤𝑎𝑣𝑒 𝑠𝑖𝑑𝑒/ 𝑝𝑜𝑠𝑡 𝑠ℎ𝑜𝑐𝑘 𝑤𝑎𝑣𝑒 𝑠𝑖𝑑𝑒
} {
𝑢𝑝 𝑠𝑡𝑟𝑒𝑎𝑚 𝑠𝑖𝑑𝑒 𝑑𝑜𝑤𝑛 𝑠𝑡𝑟𝑒𝑎𝑚 𝑠𝑖𝑑𝑒
Control volume
It is an one dimensional confinement in the medium with two surfaces i.e., pre- shock and
post- shock ,It is assumed that ,within this volume, the energy is constant.
1. Reddy Shock tube is a device used to produce and study shock waves in the laboratory.
2. Schematic labelled diagram of the original Reddy shock tube is as shown in the diagram.
𝑃2 𝑃1 x =7 cm
49 cm 51 cm
Construction :
1. RST consists of a steel tube of length 100 cm and diameter 2.9 cm.
2. A diaphragm of thickness 0.1cm divides the tube in to two compartments of length 49 cm
fitted with piston called Driver section filled with driver gas. The other compartment of
length 51 cm is called Driven section filled with driven gas.
3. Sensor S fitted to driver section measures the rupture pressure 𝑃2 ,temparature𝑇2 .
4. Two sensors 𝑆1 & 𝑆2 separated by a distance ∆𝑋 fitted to driven section measures the
pressures 𝑃4, 𝑃5 and temperatures 𝑇4 , 𝑇5 respectively.
Working :
1. Driver section is filled with gas at high pressure ( 𝑃2 )and Driven section is filled with gas
of low pressure( 𝑃1 ) .
2. Diaphragm is ruptured to produce shock waves by pushing the piston and the rupture
pressure 𝑃2 & temperature is measured using sensor S.
3. The time’𝒕′ taken by the shock wave to travel the distance ‘ x ’ is measured using sensors
𝑆1 , 𝑆2 and CRO(Cathode Ray Oscilloscope). The speed of the shock waves is calculated
𝒙
using V = .
𝒕
4. Then if a is the speed of sound at laboratory temperature, the match number of the shock
𝑽
waves is calculated using M =
𝒂
5. The Mach number increases with the increase of the thickness of the diaphragm.
Weak shock waves are produced by burst of crakers / balloons, & Motor vehicles
Strong shock waves are produced by , Supersonic jets ,Rockets, Fighter planes
Q: Uses of Shock waves.
1. Shock waves (SW)are used in the treatment of kidney stones.
2. SW are used in the pencil industry for softening of pencil wood and dry painting.
3. Sw are used in the extraction of sandal wood.
4. Sw are used to rejunevate/activate dried bore wells.
5. Sw are used for needleless drug delivery.
6. Sw are used to push DNA in to the cell.
7. SW are used for the treatment of orthopedic diseases.
8. SW are used to heal broken bones quickly.
*****
PROBLEMS ON OSCILLATIONS
2) Find the displacement at the end of 3 seconds and also the amplitude of oscillations
of a body executing simple harmonic motion in a straight line, if its period is 10
seconds and if its velocity is 1 m/s, at the time 2 seconds after crossing the
equilibrium position. Assume that there are no resistive forces.
Given: T= 10 𝑠, 𝑣 = 1 𝑚/𝑠, 𝑡 = 𝑡1 = 2 𝑠, a = ? , ‘ x ’ 𝑎𝑡 𝑡 = 3 𝑠
2𝜋
Using 𝑣 = a𝜔𝑐𝑜𝑠𝜔𝑡 and 𝜔 = 𝑇
𝑣𝑇 1𝑥10
We get a = 2𝜋𝑡 = 2𝑥180𝑥2 = 5.150 m
2𝜋𝑐𝑜𝑠 ( ) 2𝜋𝑐𝑜𝑠 ( )
𝑇 10
2𝜋𝑡 2𝑥180𝑥3
Also x = 𝑎𝑠𝑖𝑛𝜔𝑡 = 𝑎𝑠𝑖𝑛 ( ) = 5.15𝑠𝑖𝑛 ( ) = 4.898 m
𝑇 10
4) Evaluate the resonance frequency of a spring of force constant 2467 N/m, carrying
a mass of 100 gm.
Given: k = 2467 𝑁/𝑚, m = 100 𝑔𝑚 = 100 𝑥10−3 kg , ν= ?
𝑘
Using 𝜔 = √𝑚 and 𝜔 = 2𝜋𝜈,
1 𝑘 1 2467
We get , ν= 2𝜋 √𝑚 = 2𝜋 √100 𝑥10−3 =24.998 Hz = 25 Hz
5) Given the force constant as 9.8 N/m for a spring ,estimate the number of
oscillations it would complete in 1 minute, if it is set for oscillations with a load of
89.37 gm. Assume there are no external forces acting on it.
Given: k = 9.8 𝑁/𝑚, m = 89.37 𝑔𝑚 = 89.37 𝑥10−3 kg,
t = 1 𝑚𝑖𝑛𝑢𝑡𝑒 = 60 𝑠 , n = ?
𝑘
Using 𝜔 = √𝑚 , 𝜔 = 2𝜋𝜈
1 𝑘 1 9.8
We get , ν= 2𝜋 √𝑚 = 2𝜋 √89.37 𝑥10−3 = 1.67 Hz
∴ n = 𝜈𝑡 = 1.667 𝑥 60 = 100 oscillations
6) A mass of 4.3 gm is attached to a spring of force constant 17 N/m. This mass spring
system is executing simple harmonic oscillations. Find out the frequency of the
external force which excites resonance in the system. Ignore the mass of the spring.
Given: k = 17 𝑁/𝑚, m = 4.3 𝑔𝑚 = 4.3 𝑥10−3 kg, ν = ?
𝑘
Using 𝜔 = √𝑚 , 𝜔 = 2𝜋𝜈
1 𝑘 1 17
We get , ν= 2𝜋 √𝑚 = 2𝜋 √4.3 𝑥10−3 = 10.03 Hz= 10 𝐻𝑧
7) A mass of 200 gm is attached to a spring of negligible mass and the system is set for
vibrations. If the damping constant for the system is 0.16 kg/s. then what will be
the time required for the vibration amplitude to decay to 1/e of its starting
amplitude. Estimate the number of vibrations the body executes meanwhile, it the
force constant is 126 N/m.(Assume the damping to be small)
8) A tuning fork has a natural frequency of 512 Hz. A periodic force per unit mass
5x10−2 N/kg acts on it. Calculate the maximum amplitude attained by the fork if the
damping per unit mass is 2x10−2 rad/s
𝑟
Given: F/𝑚 = 5𝑥10−2 𝑁/𝑘𝑔, 𝜈 = 512 𝐻𝑧,2b = = 2x10−2 rad/s, 𝑎𝑚𝑎𝑥 = ?
𝑚
𝐹/𝑚 𝐹/𝑚 5𝑥10−2
Using , 𝑎𝑚𝑎𝑥 = 2𝑏𝜔 = 2𝑏2𝜋𝜈 = (2𝑥10−2 )2𝜋512 = 7.77 x10−4m= 0.777𝑚𝑚
1 𝑘 1 17
Se get, ν = √ = √ = 10.007 Hz
2𝜋 𝑚 2𝜋 4.3𝑥10−3
1. The distance between the two pressure sensors in a shock tube is 100 [Link] time taken
by a shock wave to travel this distance is 200 [Link] the velocity of sound under
the same conditions is 340 m/s. find the Mach number of the shock wave.
Given: x =100 mm=100x10−3 m,t =200μS=200𝑥10−6 S,a=340 m/s ,M=?
𝑋 𝑉
Using, ,V= and M =
𝑡 𝑎
M = 1.228 x 10−10 m
3. The distance between two pressure sensors in a shock tube is 150 mm. The
Time taken by a shock wave to travel this distance is 0.3 [Link] the velocity
of sound under the same condition is 340m/s. Find the Mach number of the
shock wave.
4. The distance between the two pressure sensors in a shock tube is 100 mm. The time
taken by a shock wave to travel this distance is 100 microsecond. If the velocity of sound
under the same conditions is 340 m𝑠 −1 , find the Mach number of the shock wave.
(4Marks)
Module- 2 : Syllabus
4.1 Quantum Mechanics: Introduction to black body radiation spectrum, Wien’s, R-J law, No numerical problems
Stefan-boltsman law, Planck’s law.
Deduce Wiens law and R-J law from Planck’s law. No numerical problems
Wave nature of particles-De Broglie hypothesis followed by wavelength equations, extended to Numerical
accelerated electron problems
Heisenberg's uncertainty principle-Statement and mention the three uncertainty relations. Numerical
Applications of uncertainty principle- to show the non confinement of electrons in the nucleus problems
(by considering diameter of nucleus). Energy relativistic equation shall not be considered.
Schrodinger's time independent wave equation -Setting up of Schrodinger's time independent No numerical problems
wave equation using 𝚿 = A𝑒 𝑖(𝑘𝑥−𝜔𝑡)
Significance of Wave function -qualitative statement regarding wave function, Probability No numerical problems
density, Max born interpretation, Normalization, and Properties of wave
Function
Application Schrodinger's wave equation to particle in 1D potential well of infinite height and Numerical
obtain the energy Eigen values and Eigen functions. Probability densities problems
Tutorial classes , ~ Involvement of students in respect of their doubts about the
module and numerical problems
Module-2
1. Explain Black body radiation spectrum.
2. Deduce Wien’s law and R-J law from Planck’s law.
3. What are de-Broglie waves? Deduce the expression for de- Broglie wavelength of an electron.
4. State and explain HUP and hence (using HUP) show that electrons are non-exist in the nucleus.
5. Set up 1D Schrodinger time independent wave equation using Ψ = 𝑨𝒆𝒊(𝒌𝒙−𝝎𝒕)
6. Application of Schrodinger time independent wave equation for a particle in 1D potential well
of infinite depth.
7. Wave function and its properties.
MODULE-2
QUANTUM MECHANICS
Quantum mechanics is an important tool to study atomic and subatomic states. In contrast
to classical mechanics, Quantum mechanics deals with the physics of atomic and nuclear
systems. The atomic phenomenon cannot be explained in terms of classical notations,
hence Quantum mechanics put forward to explain atomic systems.
Q:What is meant by Black Body radiation spectra ? explain it briefly.
Black body: A black body is one which absorbs all the radiation incident on it
irrespective of wavelength and on heating it emits all the radiation.
Rayleigh-Jean’s law
Wein’s law
𝟎 𝝀𝒎 𝝺
1. If we plot intensity of the thermal radiations emitted by a Black Body against the
corresponding wave lengths at different temperatures, we get Black body radiation
(BBR)spectra as shown in the graph.
2. From the graph it is clear that the wavelength (𝜆𝑚 ) corresponding to the maximum
intensity 𝑬𝒎 varies inversely as the absolute temperature(T ) of the black body. This is
𝟏
called Wein’s displacement law , 𝒊𝒆: 𝝀𝒎 ∝ 𝑻 or 𝝀𝒎 𝑻 = 𝒄𝒐𝒏𝒔𝒕𝒂𝒏𝒕 According to this law
′𝜆𝑚 ′ shifts towards shorter wavelength side with the increase of ‘ T ’ of the body.
3. Wein’s law states that the energy density in the wave length interval λ & λ +dλ
is 𝑼𝝀 dλ = 𝑪𝟏 𝝀−𝟓 𝒆−𝑪𝟐 /𝝀𝑻 dλ where 𝐶1 & 𝐶2 are constants. Wein’s law explained
only the shorter wavelength region of BBR spectra below 𝜆𝑚 and it failed to
explain the longer wavelength region of the BBR spectra beyond 𝜆𝑚 .
4. Rayleigh-Jean’s law states that the energy density in the wave length interval λ &
𝟖𝝅𝒌𝑻
λ +dλ is 𝑼𝝀 dλ = dλ, where k = Boltzmann’s constant. Rayleigh-Jean’s law
𝝀𝟒
explained the longer wavelength region of BBR spectra beyond 𝜆𝑚 and it failed
explain the shorter wavelength region of BBR spectra below 𝜆𝑚 .
5. Stefan- Boltzmann radiation law states that total energy density E of radiation emitted
from a black body is directly proportional to the fourth power of its absolute
temperature T. Energy density E is defined as the total energy emitted at all wavelengths
per unit area of the emitted surface.
i.e., E ∝ T4
E = σ T4 where σ = 5.67 X 10-8 Jm-2s-1k-4
This law agrees well with the experimental results.
6. Planck’s law states that, “ the emission or absorption of radiation by matter takes place not
as a continuous process but discrete units of energy called ‘quanta’. If ν is the frequency of
radiation, E=hν, the particle which has this quanta of energy is called Photon.
Assumptions :
1. The BB chamber is filled with simple harmonic oscillators or resonators which can
vibrate with all possible frequencies.
2. An oscillator can have a discrete set of energies which are integral multiples of a finite
quantum of energy, E=hν, where n is quantum number.
3. An oscillator radiates or absorbs energy only when it changes quantum states. If it
remains in one quantum state, no energy is absorbed or emitted.
Using above assumptions ,Planck’s derived a relation given by,
the energy density in the wavelength interval λ & λ +dλ is
𝟖𝝅𝒉𝒄 𝟏
𝑬𝝀 dλ = 𝒉𝒄 dλ .
𝝀𝟓 ( )
𝒆 𝝀𝒌𝑻 −𝟏
Planck’s law explained the BBR spectra completely ie: both shorter and longer
wavelength sides of the spectra.
Q:Deduce/derive Wein’s law & Rayleigh-Jeans law from planck’s law of radiation or
Reduce Planck’s law to Wein’s law and Rayleigh-Jeans law
8𝜋ℎ𝑐 1
Planck’s law of radiation is given by 𝑈𝜆 dλ = ℎ𝑐 dλ ……………(1)
𝜆5 ( )
𝑒 𝜆𝑘𝑇 −1
a) Wein’s law:
ℎ𝑐
( )
For shorter wave lengths, ‘λ ‘is very small ,hence 𝑈𝜆 & 𝑒 𝜆𝑘𝑇 are
ℎ𝑐 ℎ𝑐 ℎ𝑐
( )
Large i.e: 𝑒 𝜆𝑘𝑇 ≫ 1 so that 𝑒 (𝜆𝑘𝑇) − 1 = 𝑒 (𝜆𝑘𝑇) ……….(2)
8𝜋ℎ𝑐 1
∴ from eqn 1 &2,we get 𝑈𝜆 dλ = ℎ𝑐 dλ
𝜆5 ( )
𝑒 𝜆𝑘𝑇
𝑪𝟐 ℎ𝑐
∴ 𝑼𝝀 dλ = 𝑪𝟏 𝝀−𝟓 𝒆−𝝀𝑻 dλ 𝑇ℎ𝑖𝑠 𝑖𝑠 𝑤𝑒𝑖𝑛’𝑠 𝑙𝑎𝑤 .where 𝐶1 = 8𝜋ℎ𝑐 & 𝐶2 =
𝑘
b) Rayleigh-Jeans law:
8𝜋ℎ𝑐 1
∴ from eqn 1 &3,we get 𝑈𝜆 dλ = ℎ𝑐 dλ
𝜆5
𝜆𝑘𝑇
𝟖𝝅𝒌𝑻
𝒊𝒆: 𝑼𝝀 dλ = dλ , 𝑇ℎ𝑖𝑠 is Rayleigh-Jeans law
𝝀𝟒
3. This failure of R-J’s law beyond ultra-violet region is called “ultraviolet catastrophe”.
The K.E of an electron of mass ‘m’, charge ‘e’ accelerated in a potential ‘V’ volt is given
1
by 𝑚𝑣 2 = 𝑒𝑉 , multiplying both Nr. and Dr. of LHS by ‘m’
2
𝑚2 𝑣 2
we get, = 𝑒𝑉
2𝑚
𝑖𝑒; 𝑚2 𝑣 2 = 2𝑚𝑒𝑉
𝑃2 = 2𝑚𝑒𝑉 ∵ 𝑚𝑣 = 𝑃
𝑷 = √𝟐𝒎𝒆𝑽
𝒉 𝒉
But λ = ∴ 𝝀=
𝑷 √𝟐𝒎𝒆𝑽
𝟔.𝟔𝟐𝟓𝒙10−34
=
√𝟐𝒙 𝟗.𝟏𝒙𝟏𝟎−𝟑𝟏 𝒙𝟏.𝟔𝒙𝟏𝟎−𝟏𝟗 𝑽
𝟏.𝟐𝟐𝟖𝒙𝟏𝟎−𝟗
= m
√𝑽
1.228 𝟏𝟐.𝟐𝟖
= 𝑛𝑚 = Å
√𝑽 √𝑽
Properties of Matter waves :
1. Matter waves cannot be observed.
2. Waves associated with microscopic particles such as electrons can be measured.
3. Matter waves are not electromagnetic waves in nature.
4. They propagate as group of waves.
Q: State & explain Heisenberg’s Uncertainty Principle (HUP). Mention its significance.
HUP states that “It is impossible to determine simultaneously both the position and
momentum of a particle with accuracy”. The product of the uncertainties in the
simultaneous measurement of the position (Δ𝑥) in the position and momentum(ΔP𝑥) of a
particle is equal to or greater than ( h/4𝛑) “
𝒉
i.e.: Δ𝑥 ΔP𝑥 ≥ ,Where h is Planck’s constant.
𝟒𝝅
The significance of HUP is that, it is impossible to determine simultaneously both the position and
momentum of the particle accurately at the same instant.
𝒉
NOTE : Other HUP relations are ∆𝑬.∆𝒕 ≥ , 𝑤ℎ𝑒𝑟𝑒 ∆𝐸 = 𝑒𝑛𝑒𝑟𝑔𝑦, ∆𝑡= time,
𝟒𝝅
𝒉
& ∆𝑳.∆𝜽 ≥
𝟒𝝅
where , ∆𝐿 = 𝑢𝑛𝑐𝑒𝑟𝑡𝑎𝑖𝑛𝑖𝑡𝑦 𝑖𝑛 𝑎𝑛𝑔𝑢𝑙𝑎𝑟 𝑚𝑜𝑚𝑒𝑛𝑡𝑢𝑚 & ∆𝜃 =
𝑢𝑛𝑐𝑒𝑟𝑡𝑎𝑖𝑛𝑖𝑡𝑦 𝑖𝑛 𝑑𝑖𝑠𝑝𝑙𝑎𝑐𝑒𝑚𝑒𝑛𝑡.
Physical significance of HUP:
1. It introduces the concept of probability.
2. It can be used to find life time of electrons in an excited states.
3. It can be used to show that electrons do not exist inside the nucleus.
Q: Show that electrons do not present in the nucleus using Heisenberg’s Uncertainty Principle.
In radioactivity three kinds of particles are emitted α,β,γ- rays. β-particles are electrons, hence
it was thought that electrons may reside inside the nucleus. If Electron to be present in the
nucleus, maximum uncertainty in position Δ𝑥=10-14 m (diameter)
According to HUP,
ℎ
The minimum uncertainty in momentum ΔP𝑥 ≥
4𝜋 𝛥𝑥
6.625 𝑥 10−34
≥
4 𝑥 3.14 𝑥 10−14
ΔP𝑥 ≥ 0.5 x 10-20 kg m/s = P(say)
The minimum energy of the electron in the nucleus is given by
𝑃2
∴ E ≥ 2𝑚
(0.5𝑥 10−20 )2
≥ 2𝑥9.11𝑥10−31
≥ 1.372 x10−11 J
𝟏.𝟑𝟕𝟐𝒙𝟏𝟎−𝟏𝟏
≥ MeV
1.6 𝑥 10−13
≥ 𝟖𝟓 𝑴𝒆𝑽
But the maximum kinetic energy of the electrons(𝛃-particle) emitted from the nucleus
does not exceed 4MeV, hence electrons do not present in the nucleus.
A satisfactory interpretation of the wave function 𝛹 associated with a moving particle was
given by Max Born in [Link] Born postulated that the square of the magnitude of the wave
function |𝛹|2 ( or 𝛹𝛹 ∗ If 𝛹 is complex)
Evaluated at a particular point represents the probability of finding the particle at that point.
|𝛹|2 is called probability density and 𝛹 is called the probability amplitude.
According to Max Born interpretation the probability of finding the particle in space is given by
+∞
∫−∞ |𝛹|2 𝑑𝑣 = 1
Any wave function that obeys this equation is said to be’normalised’. Every acceptable wave
function must be normalisable.
The normalized function must be Finite, Single valued and continuous everywhere.
Q: Set up 1D time independent Schrodinger wave equation for a free particle.
One dimensional wave function 𝚿 for the de-Broglie wave of a particle moving
along the positive direction of 𝑥-axis is given by 𝚿 = A𝑒 𝑖(𝑘𝑥−𝜔𝑡)
= A𝑒 𝑖𝑘𝑥 𝑒 −𝜔𝑡 ,
Where A𝑒 𝑖𝑘𝑥 represent the time independent part of the wave function and is
represented by 𝜓 = A𝑒 𝑖𝑘𝑥 …… (1) differentiating eqn (1) w.r.t ‘𝑥 ‘ twice we get
𝑑𝜓
= 𝐴(𝑖𝑘) 𝑒 𝑖𝑘𝑥 and
𝑑𝑥
𝑑2𝜓
=A(𝑖𝑘) (𝑖𝜔) 𝑒 𝑖𝑘𝑥
𝑑𝑥 2
= 𝑖 2 𝑘 2 A𝑒 𝑖𝑘𝑥 …….(2)
From eqns 1 & 2 we get
𝑑2𝜓 4𝜋2 𝟐𝝅
=− 𝜓 ……..(3) ∵ 𝒊𝟐 = −1 & 𝒌 =
𝑑𝑥 2 𝜆2 𝝀
ℎ
But, de-Broglie wave length λ = 𝑚𝑣
1 𝑚2 𝑣 2
∴ =
𝜆2 ℎ2
2𝑚(½𝑚𝑣 2 )
=
ℎ2
also,the kinetic energy in terms of the total energy (E) & the potential energy( V) is given
by (½𝑚𝑣 2 =(E−𝑽)
1 2𝑚(𝐸−𝑽)
∴ = ……(4)
𝜆2 ℎ2
𝑑2 𝜓 4𝜋2 2𝑚(𝐸−𝑽)
From eqns 3 & 4 ,we get =− 𝜓
𝑑𝑥 2 ℎ2
𝒅𝟐 𝝍 𝟖𝝅𝟐 𝒎(𝑬−𝑽)
+ 𝝍 = 𝟎 ……(5)
𝒅𝒙𝟐 𝒉𝟐
This is Schrodinger time independent equation for a particle
For a free particle ,V=0
𝑑2𝜓 8𝜋2 𝑚𝐸
∴ + 𝜓=0
𝑑𝑥 2 ℎ2
This is Schrodinger time independent equation for free particle.
Q: Obtain normalized wave function for a free particle in a infinite walled potential
Box/Well using Schrodinger 1D time independent equation.
∞ ∞
V=∞ V=0
Box/Well ●
particle
𝑥=0 𝑥=a
Consider a particle of mass ‘m’ moving by reflection at infinitely high walls of a Box/well
of width ‘a’ moving between 𝑥=0 & 𝑥=a Potential V=0 inside the Box/well and V=∞
outside the Box/well .one dimensional Schrodinger equation for particle is given by
𝑑2𝜓 8𝜋2 𝑚(𝐸−𝑽)
+ 𝜓 = 0 ……(1).
𝑑𝑥 2 ℎ2
For a particle inside the Box/well V=0
𝑑2𝜓 8𝜋2 𝑚𝐸
∴ + 𝜓 = 0 ….(2)
𝑑𝑥 2 ℎ2
8𝜋2 𝑚𝐸
Putting = 𝐾 2 …..(3) in equation (2) ,
ℎ2
2
𝑑 𝜓
we get + 𝐾 2 𝜓 = 0 ……(4)
𝑑𝑥 2
The general solution of the quadratic equation (4) is of the form ψ (𝑥)=C Cos(K𝑥) +D sin(K𝑥)
……(5)
where A & B are constants determined from boundary conditions as follows :
ψ (𝑥)=0 at 𝑥=0 from eqn (5), 0= C x 1 + D x 0
∴ C=0
also, ψ (𝑥)=0 at 𝑥=a ∴ from eqn(4) 0=C Cos(Ka)+D Sin(Ka)
0= D Sin(Ka)
Sin(Ka) = 0 as D≠ 0
∴ Sin(Ka) =0= Sin(n𝜋)
𝑛𝜋
ie: Ka=n𝜋 or K= 𝑎 …..(6)
8𝜋2 𝑚𝐸 𝑛2 𝜋 2
From eqns 3 & 6 ,we get =
ℎ2 𝑎2
𝑛2 ℎ 2
∴ E = 8𝑎2 𝑚 or
𝒏𝟐 𝒉𝟐
In general En= …(7)
𝟖𝒂𝟐 𝒎
where n=1,2,3..called quantum number.
The values of En are called Eigen energy values which satisfy Schrodinger wave equation.
𝑛𝜋
Substituting the values of C=0 & K= in eqn 5, we get
𝑎
𝜓𝑛 (𝑥) = A Sin( 𝑛𝜋𝑥
𝑎
) …….(8)
To find ’D’ by normalization:
+∞
Applying the normalization condition ∫−∞ 𝐼𝛹𝐼 2 𝑑𝑥 = 1 to eqn 8 for x=0 & x=a, we get
𝑎
∫0 𝐷2 𝑆𝑖𝑛2 ( 𝑛𝜋𝑥
𝑎
)𝑑𝑥 = 1
𝑎
𝐷2 ∫0 ½[1 − 𝐶𝑜𝑠 ( 2 𝑛𝜋𝑥
𝑎
)]𝑑𝑥 = 1 ∵ 𝑆𝑖𝑛2 (𝜃)=½[1-Cos(2𝜃)]
𝑎 𝑎
½𝐷2 [∫0 1𝑑𝑥 − ∫0 𝐶𝑜𝑠( 2 𝑛𝜋𝑥
𝑎
)𝑑𝑥 ] = 1
𝑎 2𝑛𝜋𝑥 𝑆𝑖𝑛(𝑚𝑥)
½𝐷2 { [𝑥]𝑎0 − [2𝑛𝜋 Sin( )]𝑎0 } = 1 ∵ ∫ 𝐶𝑜𝑠(𝑚𝑥) 𝑑𝑥 =
𝑎 𝑚
2 𝑎 𝑎
½𝐷 { [𝑎 − 0] − [2𝑛𝜋 Sin(2n𝜋) − Sin(0)] }=1
2𝑛𝜋
½𝐷2 { [𝑎 − 0] − [0 − 0] }=1
𝐷2 𝑎 = 2 ⇨ 𝐷2 = 2/𝑎 or D =√𝟐/𝒂 …(9)
From eqns 8 &9, the normalized Eigen functions are 𝑔𝑖𝑣𝑒𝑛 𝑏𝑦 𝝍𝒏 (𝑥)= √𝟐/𝒂 Sin( 𝒏𝝅𝒙
𝒂
) …..(10)
Eigen energy values and Eigen wave functions :
Any wave function 𝚿 which satisfies Schrodinger’s equation and having properties that they are
single valued, finite everywhere, continuous every where and also their first order derivatives
should posses above properties are called Eigen wave functions or Eigen functions
Eigen value is the energy of a particle in corresponding to its Eigen functions.
Eigen energy values are the energy values which satisfy Schrodinger wave equation and
𝑛2 ℎ 2
are given by En=
8𝑎2 𝑚
ℎ2
For n=1 gives E1 = 8𝑎2𝑚 = Eo called end point /ground state energy .
4ℎ2
n=2 gives E2 = 8𝑎2𝑚 = 4 Eo called 1st excited state energy
9ℎ2
n=3 gives E3 = 8𝑎2𝑚 =9 Eo ,called 2nd excited state energy & so on
Eigen wave functions are the wave functions which have single finite value and continuous
Everywhere and is given by 𝜓𝑛 (𝑥)= √2/𝑎 Sin( 𝑛𝜋𝑥
𝑎
)
𝑛 = 3 𝝍3 𝐼𝝍3 𝐼 2
.
𝑛 = 2 𝝍2 𝐼𝝍2 𝐼 2
𝑛 = 1 𝝍1 𝐼𝝍1 𝐼 2
𝑥=0 𝑥=a 𝑥=0 𝑥=a
2 2 2
𝐸𝑖𝑔𝑒𝑛 𝑓𝑢𝑛𝑐𝑡𝑖𝑜𝑛𝑠 𝝍1 , 𝝍2 , 𝝍3 , … . 𝑎𝑛𝑑 𝑡ℎ𝑒𝑖𝑟 𝑝𝑟𝑜𝑏𝑎𝑏𝑖𝑙𝑖𝑡𝑦 𝑑𝑒𝑛𝑠𝑖𝑡𝑖𝑒𝑠 𝐼𝝍1 𝐼 , 𝐼𝝍2 𝐼 , 𝐼𝝍3 𝐼 …
are represented as shown in the [Link] probability of finding the particle at the
anti-nodes is maximum and at nodes is zero.(The particle never found at nodes)
ℎ
Formulae needed : λ = where P = mv = √2𝑚𝐸 =√2𝑚𝑒𝑉 ,
𝑃
1 𝑃2 ℎ𝐶 ℎ
E = 𝑚𝑉 2 = ;Photon energy E = hν = ; ∆𝑥. ∆𝑃𝑥 ≥ and
2 2𝑚 𝜆 4𝜋
ℎ ℎ𝐶∆𝜆
∆𝑝 = 𝑚. ∆𝑣 ; ∆𝐸. ∆𝑡 ≥ 𝑎𝑛𝑑 ∆𝐸 = ; also ∆𝐸 = ℎ ∆𝜈 ;
4𝜋 𝜆2
𝑥 𝑛2 ℎ 2
P = ∫𝑥 2 𝐼𝛹𝐼 2 dx ; 𝐸𝑛 =
1 8𝑚𝑎2
1. Compare the energy of a photon with that of an electron when both are associated with
wavelength 0.2 nm.
Given: 𝜆𝑃 = 𝜆𝑒 = 0.2 𝑛𝑚 = 0.2𝑥10−9 𝑚 , h=6.63x10−34 Js, m=9.1x10−31 kg ; C=3x108 m/s,
𝐸𝑃
=?
𝐸𝑒
ℎ𝐶 ℎ2
Using 𝐸𝑃 = and 𝐸𝑒 =
𝜆𝑃 2𝑚𝜆𝑒 2
𝐸𝑃 𝐶2𝑚𝜆𝑒 2
We get , =
𝐸𝑒 ℎ𝜆𝑃
3𝑥108 𝑥2𝑥9.1𝑥10−31 ( 0.2𝑥10−9 )2
=
6.63𝑥10−34 𝑥 0.2𝑥10−9
= 1.647x 102
2. Calculate the kinetic energy of an electron of wavelength 18 nm.
Given: 𝜆 = 18 𝑛𝑚 = 18𝑥10−9 𝑚 , h=6.63x10−34 Js, m=9.1x10−31kg ; E= ?
ℎ
Using λ =
√2𝑚𝐸
ℎ2
We get ,𝐸 =
2𝑚𝜆2
( 6.63𝑥10−34 )2
=
2𝑥9.1𝑥10−31 𝑥( 18𝑥10−9 )2
= 7.454x10−22 J
7.454𝑥10−22
=
1.6𝑥10−19
= 4.66x10−3 eV
3. An excited atom has an average life time of 10−8 seconds. During this period. it emits
photon and returns to the ground state. What is the minimum uncertainty in the frequency
of this photon ?
ℎ
Using λ =
𝑚𝑣
6.63𝑥10−34
=
9.1𝑥10−31 𝑥0.01𝑥 3𝑥108
= 2.43 x10−10 m
5. An electron is bound in one dimensional infinite well of width [Link] the
energy value and de-Broglie wavelength in the first excited state.
Given: a = 0.12nm = 0.12x10−9 m ; n = 2 ; h=6.63x10−34 Js; 𝑚 = 9.1𝑥10−31 𝑘𝑔 ;
𝐸2 = ? & λ =?
𝑛2 ℎ 2
Using 𝐸𝑛 =
8𝑚𝑎2
22 (6.63𝑥10−34 )2
𝐸2 =
8𝑥9.1𝑥10−31 𝑥(0.12𝑥10−9 )2
= 1.68x10−17 J
ℎ
Also , λ =
√2𝑚𝐸2
6.63𝑥10−34
=
2𝑥9.1𝑥10−31 𝑥1.68𝑥10−17
= 1.19 x10−10 m
6. Calculate the de-Broglie wavelength associated with an electron of energy 1.5eV.
7. A spectral line of wavelength 5461Å has a width of 10−4Å. Evaluate the minimum time
spent by the electrons in the upper energy state.
ℎ𝐶 ℎ
Using ∆𝐸 = and ∆𝐸. ∆𝑡 ≥
𝜆 4𝜋
𝜆
We get , ∆𝑡 ≥
4𝜋.𝐶
5461𝑥10−10
≥
4𝑥𝜋𝑥3𝑥108
= 1.45 x 10−16 S
6.63𝑥10−34
=
1𝑥1
= 6.63x10−34 𝑚
Comment : Wavelength is inversely proportional to the mass ,as 𝜆𝑒 ≫ 𝜆0
9. A quantum particle confined to one-dimensional box of width ‘a’ is in its first excited
𝑎
state. What is the probability of finding the particle over an interval of ( 2 ) marked
symmetrically at the centre of box.
𝑎 3𝑎
Given: 1st excited state , n=2 ;the interval ( , )
4 4
2
𝑥2 3𝑎/4 2
Using P = ∫𝑥1 𝐼𝛹𝐼2 dx = ∫𝑎/4 [√𝑎 𝑆𝑖𝑛 ( 2𝜋𝑥
𝑎
)] 𝑑𝑥 𝑎/2
3𝑎
𝟐
= ∫𝑎4 𝒂 𝑆𝑖𝑛2 ( 2𝜋𝑥
𝑎
)𝑑𝑥 0 a/4 a/2 3a/4 a
4
3𝑎
𝟐
= 𝒂
∫𝑎4 ½[1 − 𝐶𝑜𝑠 ( 4 𝑎𝜋𝑥 )]𝑑𝑥 ∵ 𝑆𝑖𝑛2 (𝜃)=½[1-Cos(2𝜃)]
4
3𝑎 3𝑎
𝟐
= ½ 𝒂 ∫𝑎4 1𝑑𝑥 − ∫𝑎4 𝐶𝑜𝑠( 4 𝑎𝜋𝑥 )𝑑𝑥
4 4
3𝑎 3𝑎
𝑎 4𝜋𝑥
= 𝑎 { [𝑥] 𝑎
4
− [4𝜋 Sin( 𝑎
)]𝑎
4
}
4 4
3𝑎 𝑎
4𝜋 𝑎 4𝜋
= 𝑎 { [3𝑎
4
− 𝑎4] − [4𝜋
𝑎
Sin( 4
𝑎
)− 2𝜋 Sin( 𝑎
4
)] }
𝑎
= 𝑎 { [3𝑎
4
− 𝑎4] − [4𝜋
𝑎
Sin(3𝜋)− 2𝜋 Sin(𝜋)] }
𝑎
= 𝑎 { [2] − [0 − 0 } = ½ = 0.5 or 50%
10. A particle moving in one dimension box is described by the wave function 𝛹 = 𝑥[√3] 𝑓𝑜𝑟
0<𝑥<1 and Ψ =0 elsewhere. Find the probability of finding the particle within the
interval (0,½).
1
Given : 𝛹 = 𝑥[√3] ; (𝑥1 , 𝑥2 )( 0, 2 ) ; P = ?
𝑥
Using Probability, P = ∫𝑥 2 𝐼𝛹𝐼 2 dx
1
1
1
𝑥3 1 1
= ∫0 3𝑥 2 2
dx = [3. ]20 = ( )3 – (0)3 = = 0.125 or 12.5 %
3 2 8
11. Find the energy of the neutron in eV whose de-Broglie wavelength is 1Å.
ℎ
Using , λ =
√2𝑚𝐸
ℎ2
We get , E = joules
2𝑚𝜆2
ℎ2
= eV
2𝑚𝑒𝜆2
(6.63𝑥10−34 )2
=
2𝑥1.678𝑥10−27 𝑥1.6𝑥10−19 𝑥(1𝑥 10−10 )2
= 0.082 eV
12. An electron is confined to a box of length 10−9 m, calculate the minimum uncertainty in it’s
velocity.
ℎ
Using ∆𝑥. ∆𝑝 ≥ and ∆𝑝 = 𝑚. ∆𝑣
4𝜋
ℎ
We get , ∆𝑣 ≥
4𝜋𝑚∆𝑥
6.63𝑥10−34
≥
4𝜋 𝑥9.1𝑥10−31 𝑥10−9
= 58 x103 m/S
13. Compute the de-Broglie wavelength for a neutron moving with one tenth part of the
velocity of light.
𝐶 3 𝑋 108
Given; V = = = 0.3 𝑥 108 𝑚/𝑠;h=6.63x10−34 Js, m=1.678x10−27kg ;
10 10
C = 3 X 108 m/s ; λ = ?
ℎ
Using λ =
𝑚𝑉
6.63𝑥10−34
= = 1.317x 10−14 m.
1.678𝑥10−27 𝑥0.3 𝑥 108
14. An electron has a de-Broglie wavelength 3 nm and rest mass 511keV. Determine its group
velocity and kinetic energy.
ℎ ℎ
Using λ = ,we get 𝑉𝑔 = V =
𝑚𝑣 𝑚𝜆
6.63𝑥10−34
=
9.08𝑥10−31 𝑥3𝑥 10−9
= 2.43x 106 m/s
1 1
𝑎𝑙𝑠𝑜, 𝐸𝐾 = 2 𝑚𝑉 2 = 2 𝑥 9.08𝑥10−31 𝑥 (2.43𝑥 106 )2
= 2.681x 10−18 J
15. A spectral line of wavelength 546.1 nm has a width 10−5 nm. Estimate the minimum time
spent by electrons in the excited state during transitions.
ℎ𝐶 ℎ
Using ∆𝐸 = and ∆𝐸. ∆𝑡 ≥
𝜆 4𝜋
𝜆
𝑤𝑒 𝑔𝑒𝑡 , ∆𝑡 ≥
4𝜋.𝐶
546.1𝑥10−9
≥ = 1.45x 10−16 S
4𝜋𝑥3𝑥108
16. Calculate the momentum of the particle and de-Broglie wavelength associated with an
electron with a kinetic energy of 1.5KeV.
17. An electron is bound in one dimensional potential well of width 0.18 nm. Find the energy
value in eV of the second excited state.
𝑛2 ℎ 2 𝑛2 ℎ 2
Using 𝐸𝑛 = J OR 𝐸𝑛 = eV
8𝑚𝑎2 8𝑚𝑎2 𝑒
32 (6.63𝑥10−34 )2 32 (6.63𝑥10−34 )2
𝐸2 = 𝐸2 = −19
8𝑥9.11𝑥10−31 𝑥(0.18 𝑥10−9 )2 8𝑥9.11𝑥10−31 𝑥(0.18 𝑥10−9 )2 𝑥1.6𝑥10
= 1.675 x10−17 J = 104.7 eV
1.675 𝑥10−17
= =104.7 eV
1.6𝑥10−19
18. Calculate the energy in eV, for the first excited state of an electron in an infinite potential
well of width 2 Å .
𝑛2 ℎ 2 𝑛2 ℎ 2
Using 𝐸𝑛 = J OR 𝐸𝑛 = eV
8𝑚𝑎2 8𝑚𝑎2 𝑒
22 (6.63𝑥10−34 )2 22 (6.63𝑥10−34 )2
= = −19
8𝑥9.1𝑥10−31 𝑥(2𝑥10−10 )2 8𝑥9.1𝑥10−31 𝑥(2𝑥10−10 )2 𝑥1.6𝑥10
= 6.038x10−18 J = 37.74 eV
6.038𝑥10−18
= =37.74 eV
1.6𝑥10−19
19. Calculate the de-Broglie wavelength associated with neutron of mass 1.674 X 10−27 kg
with one tenth part of the velocity of light .
1 1
Given : v = 10 C = 10 x 3x108 m/s = 3x107 m/s; h=6.63x10−34 Js; 𝑚 = 9.11𝑥10−31 𝑘𝑔 ; 𝜆 = ?
ℎ
Using λ =
𝑚𝑣
6.63𝑥10−34
=
9.11𝑥10−31 𝑥 3𝑥107
= 2.43 x10−11 m
20. Calculate the de-Broglie wavelength of an electron moving with K.E of 50KeV.
= 5.495 x 10−12 m
221. A particle of mass 940 MeV/𝐶 2 has kinetic energy 0.5 KeV. Find its de-
Broglie wavelength , C is velocity of light.
ℎ
Using; 𝝺 =
√(2𝑚𝐸)
6.63𝑥10−34
=
√(2𝑥1.671𝑥10−27 𝑥0.5 𝑥103 𝑥1.6𝑥10−19 )
= 1.282x10−12 m
22. The first excited state energy of an electron in an infinite well is 240 eV.
what will be its ground state energy when the width of the potential
Well is doubled.
Given: 𝐸2 = 240 eV ; 𝐸1 = ?
𝑛2 ℎ 2
Using 𝐸𝑛 =
8𝑚𝑎2
22 ℎ2
𝐸2 =
8𝑚𝑎2
4ℎ2
240 =
8𝑚𝑎2
4ℎ2
𝑎2 =
8𝑚𝑥240
ℎ2
∴ a = √(480𝑚 )
12 ℎ2 480𝑚𝑥ℎ2
𝑎𝑙𝑠𝑜 , 𝐸1 = = = 15 eV
ℎ2 8𝑚𝑥4𝑥ℎ2
8𝑚(2√( ) )2
480𝑚
𝑂𝑅
𝑛2 ℎ 2 𝐸2 𝑎22 𝐸1 𝑎12 ℎ2
Using ; 𝐸𝑛 = ,we can show that = =
8𝑚𝑎2 22 12 8𝑚
𝐸2 𝑎22 240𝑎22
∴ 𝐸1 = = = 15 eV
𝑎12 22 4𝑎22 𝑥4
23. Calculate the de-Broglie wavelength associated with neutron of mass 1.674
x10−27kg with one tenth part of the velocity of light .
𝐶 3 𝑋 108
Given; V = = = 0.3 𝑥 108 𝑚/𝑠;h=6.63x10−34 Js,
10 10
m=1.674x10−27kg ; C = 3 X 108 m/s ; λ = ?
ℎ 6.63𝑥10−34
Using λ = =
𝑚𝑉 1.674𝑥10−27 𝑥0.3 𝑥 108
= 1.320x 10−14 m.
= 1.677x10−17 J = 104.83 eV
6.038𝑥10−18
=
1.6𝑥10−19
= 104.81 eV
25. Find deBroglie wavelength of a particle of mass 0.58 MeV/𝑪𝟐 has a kinetic
energy 90 eV , where C is the velocity of light.
0.58 𝑥 106 𝑒𝑉
Given: m = 0.58 MeV/𝐶 2 =
(3𝑥108 )2
0.58 𝑥 106 𝑥1.6𝑥10−19 𝐽
= = 1.0324x10−30 𝑘𝑔
(3𝑥108 )2
E = 90eV = 90𝑥1.6𝑥10−19 𝐽 ; 𝜆 = ?
ℎ
Using; 𝝺 =
√(2𝑚𝐸)
6.63𝑥10−34
=
√(2𝑥1.0324𝑥10−30 𝑥 90𝑥1.6𝑥10−19 )
= 1.2142𝑥10−10 m
ℎ ℎ𝑣 ∆𝜆 ℎ𝑐
Using ∆𝐸. ∆𝑡 ≥ and ∆𝐸 = ∵E=
4𝜋 𝜆2 𝜆
𝜆2
We get , ∆𝑡 =
4𝜋𝑐∆𝜆
(5896 𝑥10−10 )2
∴ ∆𝑡 =
4𝜋𝑥3 𝑥 108 𝑥10−5 𝑥10−10
= 9.221 x 𝟏𝟎−𝟖 S
28. Compare the energy of a photon with that of a neutron when both are associate
with a wavelength 0.25 nm,mass of neutron is 1.675 X 𝟏𝟎−𝟐𝟕 kg.
Given : 𝜆𝑝 = 𝜆𝑛 = 0.25 𝑛𝑚 = 0.25 x 10−9 m , 𝑚𝑛 = 1.675 X 10−27 kg
𝜆𝑝
h = 6.625 x 10−34 JS , C = 3 x 108 𝑚𝑠 −1 , 𝜆 = ?
𝑛
ℎ𝑐 6.625 𝑥 10−34 𝑥3 𝑥 108
Using , 𝐸𝑝 = = = 7.95 x 10−16 J
𝜆 0.25 𝑥 10−9
ℎ2 (6.625 𝑥 10−34 )2
Also , 𝐸𝑛 = 2
= 2 = 2.096 x10−21 J
2𝑚𝜆 2𝑥1.675 𝑋 10−27 𝑥 (0.25 𝑥 10−9 )
𝑬𝒑 𝟕.𝟗𝟓 𝒙 𝟏𝟎−𝟏𝟔
∴ = = 3.793 x 𝟏𝟎𝟓
𝑬𝒏 𝟐.𝟎𝟗𝟔 𝒙𝟏𝟎−𝟐𝟏
29. An electron is bound in an one dimensional potential well of width 1 Å , but of
infinite wall height. Find its energy values in the ground state and also in the
first excited states.
Given: a = 1Å = 1x10−10 m ; h=6.63x10−34 Js; 𝑚 = 9.1𝑥10−31 𝑘𝑔 ;
𝐸1 & 𝐸2 = ?
𝑛2 ℎ 2
Using 𝐸𝑛 = 8𝑚𝑎2
For ground state, n = 1
12 (6.63𝑥10−34 )2
∴ 𝐸1 = 8𝑥9.1𝑥10−31 𝑥(1𝑥10−10 )2
= 6.038x10−18 J
For 1st excited state, n = 2
22 (6.63𝑥10−34 )2
∴ 𝐸2 =
8𝑥9.1𝑥10−31 𝑥(1𝑥10−10 )2
−17
= 2.415x10 J
*****
Module- 3 : Syllabus
3.1 Laser: Brief discussion of spontaneous and stimulated processes - Explanation of the I No numerical problems
process of induced absorption, spontaneous and stimulated emission.
Einstein's coefficients (expression for energy density) -derivation of energy density in terms of Numerical
Einstein's coefficients problems
Requisites of a Laser system - a brief explanation about active medium, resonant cavity and No numerical problems
exciting system.
Conditions for laser action-To explain population inversion and meta stable state Numerical
problems
Principle: mention different modes of vibrations of CO2 explain construction and working of No numerical problems
CO 2 laser with energy level diagram experimental setup.
Principle, Construction and working of semiconductor Lasers - Explain principle, construction Numerical
and working of homo junction semiconductor laser with energy level problems
diagram and experimental setup.
Application of Lasers in Defense (Laser range finder) - qualitative explanation about application No numerical problems
of laser as laser range finder.
No numerical problems
Medical Application of Lasers in Eye surgery and Skin treatment- qualitative explanation
3.2 Optical fiber: Description of propagation mechanism of light through an optical fiber. Numerical
Angle of acceptance and numerical aperture(NA)Theory with condition for propagation problems
Modes of propagation and V- number and types of optical fibers( qualitative) Numerical
problems
Attenuation: Definition of attenuation, name the three types of attenuation, Causes of Numerical
attenuation: Explain absorption, scattering and radiation losses. Mention the expression for problems
attenuation coefficient
Application of optical fiber: Point to point communication: Explain with the help of block No numerical
diagram. Merits and de merits of optical fiber communication. problems
Optical fiber sensors: intensity based displacement sensor and Temperature sensor based No numerical
on phase modulation problems
Tutorial classes , ~ Involvement of students in respect of their doubts about the
module and numerical problems
Module-3
1. Derivation of expression for energy density in terms of Einstein’s coefficients.
2. C𝒐𝟐 laser- Principle, construction and working.
3. Semiconductor laser- Principle, construction and working.
4. Applications of laser in defense and Medical field.
5. Theory of optical fiber/Derivation of Expressions for acceptance angle and Numerical Aperture
of optical fiber.
6. Attenuation and causes for attenuation.
7. Types of optical fibers.
8. Explanation of Point to Point communication using optical fibers.
9. Explain Optical fiber sensors.
LASERS
Q: Explain Einstein’s explanation of interaction of radiation with matter (or)
Explain Induced absorption , Spontaneous emission &Stimulated emission.
Consider a system of energy density 𝑈𝜈 𝑎𝑛𝑑 Let N1 & N2 be the population of the
energy states E1 & E2 respectively so that (E2 −E1) = hν & E2 >E1
According to Einstein, radiation interacts with matter in 3 ways namely:
1) Induced absorption:
𝐸2 𝑁2 𝑨∗ •
hν ⇝ ⇒
𝐸1 •𝑨 𝑁2
Induced absorption is the phenomenon in which an atom(A) in the lower energy state E 1
absorb the incident photon of energy ‘hν’ & excite to the higher energy state E2
if (E2 −E1) = hν .
Mathematically it(induced absorption) is represented as
hν +A → 𝑨∗ or photon +atom→ 𝑎𝑡𝑜𝑚∗
[Link] emission:
𝐸2 𝑨∗ • 𝑁2
⇒ hν ⇝
𝐸1 𝑁1 𝑨•
Spontaneous emission is the phenomenon in which an atom (A) in the excited state of
energy E2 de-excite to the lower energy state E1 without any external influence by
emitting a photon of energy hν =(E2 −E1).
Mathematically, it is represented as 𝑨∗ → A + hν
Also, Rate of Spontaneous emission = 𝐴21 𝑁2
[Link] emission:
𝐸2 𝑨∗ • 𝑁2
hν ⇝ ⇨ hν ⇝+ hν ⇝
𝐸1 𝑁1 •A
𝐸2 𝑁2 •
Stimulated emission is the phenomenon in which an atom (𝑨∗ ) in the excited state of
energy E2 de-excite to the lower energy state E1 under the influence of an external photon
(hν) by emitting an identical photon of energy hν =(E2 −E1).
Mathematically,𝑖𝑡 𝑖𝑠 𝑟𝑒𝑝𝑟𝑒𝑠𝑒𝑛𝑡𝑒𝑑 𝑎𝑠 𝒉𝝂 + 𝑨∗ → A +2 hν
Also, Rate of Stimulated emission= 𝐵21 𝑁2 𝑈𝜈 ,where 𝑈𝜈 = 𝑒𝑛𝑒𝑟𝑔𝑦 𝑑𝑒𝑛𝑠𝑖𝑡𝑦 &
𝐵21 = 𝐸𝑖𝑛𝑠𝑡𝑒𝑖𝑛′ 𝑠 𝑆𝑝𝑜𝑛𝑡𝑎𝑛𝑒𝑜𝑢𝑠 𝑒𝑚𝑖𝑠𝑠𝑖𝑜𝑛 𝑐𝑜𝑒𝑓𝑓𝑖𝑐𝑖𝑒𝑛𝑡.
Q: Explain the terms : Active medium ; Population Inversion ; Pumping ; Meta stable state
and Laser Cavity( Optical resonator) Or Explain the requisites of a laser system.
𝐸2 𝑁2 • •
. hν ⇝ ⇨ ⇨ hν ⇝ hν ⇝ ⇨ 2hν ⇝ ⇝
𝐸1 • 𝑁1 • •
Spontaneous emission
8𝜋ℎ𝜈3 1
But .the energy density given by Planck’s law is 𝑈𝜈 = 3
……(4)
𝐶 ( 𝑒 ℎ𝜈/𝐾𝑇 −1)
Comparing eqns 3 & 4 ,we get 𝑩𝟏𝟐 = 𝑩𝟐𝟏
Thus coefficient of Induced absorption = coefficient of stimulated emission.
𝟖𝝅𝒉𝝂𝟑 𝑨𝟐𝟏 ℎ𝜈
and = = 𝑈𝜈 ( 𝑒 𝐾𝑇 − 1)
𝑪𝟑 𝑩𝟐𝟏
𝑨𝟐𝟏 𝟏
Thus, energy density 𝑼𝝂 =
𝑩𝟐𝟏 –𝟏] [𝒆 𝒉𝝂/𝑲𝑻
This is the expression for energy density in terms of Einstein’s coefficients or relation
between Einstein’s coefficients.
Q:Explain the fundamental mode of vibration in CO2 molecule.
In CO2 molecule there are three fundamental modes of vibrations, namely
1. Symmetric mode :
Molecular axis
O C O
Symmetric mode is the mode in which both the oxygen atoms oscillate simultaneously to
& fro about the stationary carbon atom along the molecular axis.
2. Asymmetric mode:
Molecular axis
O C O
Asymmetric mode is the mode in which both the oxygen atoms move in one direction and
the carbon atom move in the opposite direction along the molecular axis.
3. Bending mode:
Molecular axis
The internal vibrations of CO2 molecule are the combination of the above three modes.
Q:Explain the principal, construction and working of C𝑶𝟐 laser.
Construction:
1) The schematic diagram CO2 Laser is as shown in the diagram invented by CKN Patel an
Indian engineer
2) It consists of a (glass)discharge tube of length 5 m & diameter 2.5 cm filled with a
mixture of gases CO2 ,N2 ,He in the ratio [Link]
3) High DC voltage can be applied to the gas between the electrodes A&C .
4) Ends of the tube is fitted with ( NaCl ) Brewster windows to get polarized laser beam
5) Two con-focal silicon mirrors coated with aluminum are provided at the ends of the tube
which act as optical resonators.
6) Cold water is circulated through a tube surrounding the discharge tube.
Water outlet
5m
BW BW=Brewster window
𝐶4 10.6 𝜇𝑚 laser
Working: 𝐶2
1) CO2 Laser is a four level molecular gas laser which produce continuous or pulsed laser
beam.
2) It works on the principle of stimulated emission between the rotational sublevels of an
upper & lower vibrational levels of CO2 molecules.
3) Ionisation takes place due to electric discharge when high DC voltage is applied between
electrodes producing electrons.
4) The accelerated electrons excite both N2& CO2 atoms to their higher energy levels ‘ 𝓥 =1 &
C5 from their ground states 0 & C1 due to collision as follows:
e+𝑵𝟐 → 𝑵∗𝟐 +e’ and e+𝑪𝑶𝟐 → 𝑪𝑶∗𝟐 +e’
where e& e ’are the energies of electron before and after collision.
∗
5) 𝑵𝟐 molecule in excited level collide with CO2 molecules in their ground state C1 &
excite it to metastable state C5 by resonant energy transfer as level C5 of CO2 is same as
level 𝓥=1 of 𝑁2 given by 𝑵∗𝟐 +𝑪𝑶𝟐 → 𝑪𝑶∗𝟐 +𝑵𝟐
6) As this process continues due to electric discharge pumping , population inversion takes
place betweenC5 &C4 and C5 & C3.
7) The transitions/de-excitations takes place as follows:
C5 → C4 producing laser 10.6𝜇𝑚 (IR region)
C5 → C3 producing laser 9.6𝜇𝑚 (IR region)
C4 → C2
C3 → C2 Radiation less transitions
C2 → C1
8) Due to high thermal conductivity of He, it removes heat from mixture and de-populate the
lower states C3 &C2 quickly .
9) Laser beam is amplified by using optical resonators.
10) The laser output is 100kW for continuous mode and 10 kW in pulsed mode.
Q: Explain the Principle,construction and working of Semi-conductor laser.
Construction:
1. The schematic diagram of GaAs semi-conductor device is as shown in the diagram.
2. It consists of heavily doped n-region of GaAs doped with tellurium and p-region of GaAs
doped with zinc.
3. The upper and lower surfaces are metalized so that pn-junction is forward biased .
4. Two surfaces perpendicular to the Jn are polished so that they act as optical resonators
and the other two surfaces roughened to prevent lasing in that direction.
Working:
1. Semi-conductor laser are made up of highly de-generate semi-conductors having direct
band gap like Gallium Arsenide (GaAs).
2. When GaAS diode is forward biased with voltage nearly equal to the energy gap voltage,
electrons from n-region & holes from p-region flow across the junction creating
population inversion in the active jn region.
3. As the voltage is gradually increased due to forward biasing population inversion is
achieved between the valence band and conduction band which in turn result in
stimulated emission.
4. Photons produced are amplified between polished optical resonator surfaces producing
laser beam.
5. GaAs laser produce laser beam of wavelength 8870Å in IR region , GaAsP produce laser
beam of 6500Å in visible region etc.
Semiconductor laser Energy level giagram
RS
𝐸𝐹𝑒
PS CB
P-type
Ba p P Laser
Pn-jn 𝐸𝐹𝑝 h+e
n-type VB
n-type
Polished surfac(PS)
Laser
Roughened surface(RS)
MC
Transmitted laser
TARGET
Antenna
S Reflected laser
Laser
Transmitter/Receiver
TV Monitor
Target Image
OPTICAL FIBRES
Acceptance angle is the maximum angle submitted by the ray with the axis of the fiber so
that light can be accepted and guided along the fiber.
Consider the special case of a ray which suffers critical incidence at the core cladding
interface. The ray to begin with travels along AO entering into the core at an angle 𝜃𝑜 to
the fiber axis. Then it is refracted along OB at an angle 𝜃1 in the core and further proceeds
to fall at critical angle of incidence( equal to 90- 𝜃1 ), 𝑖𝑡 𝑔𝑟𝑎𝑧𝑒𝑠 𝑡ℎ𝑒 𝑠𝑢𝑟𝑓𝑎𝑐𝑒.
It is clear from the fig that, any ray that enters into the core at an angle of incidence less
than 𝜃𝑜 , will have refractive angle less than 𝜃1 because of which its angle of
incidence(=90- 𝜃1 ) at the interface, will become greater than the critical angle of
incidence and undergoes TIR. The NA represents the light gathering capability of the
optical fiber.
Condition for propagation: Let 𝑛1 , 𝑛2 & 𝑛𝑜 be the RI of core, cladding and launch medium
respectively. Now , for refraction at the point of entry of the ray AO into the core, By snell’s
𝑛1
law at A, 𝑛𝑜 𝑠𝑖𝑛 𝜃0 = 𝑛1 𝑠𝑖𝑛 𝜃1 ⇨ 𝑠𝑖𝑛 𝜃0 = 𝑠𝑖𝑛 𝜃1 ……(1)
𝑛𝑜
𝑛1 𝑐𝑜𝑠 𝜃1 = 𝑛2
𝑛
𝑐𝑜𝑠 𝜃1 = 𝑛2 ……….(2)
1
𝑛1
Rewriting equation (1), 𝑠𝑖𝑛 𝜃0 = 𝑠𝑖𝑛 √(1 − 𝑐𝑜𝑠 2 𝜃1 ) ….(3)
𝑛𝑜
𝑛1 2 √𝑛12 −𝑛22
Sub eqn (2) in (1) we get, 𝑠𝑖𝑛 𝜃0 = √(1 − ( 𝑛2 ) ) =
𝑛𝑜 𝑛 1 𝑛0
Numerical aperture is the ability of the optical fiber to accept the light and guide
along the fiber and is numerically equal to sine of the acceptance angle.
√𝑛12 −𝑛22
ie: NA = 𝑠𝑖𝑛 𝜃𝑜 = 𝑛𝑜
if 𝜃𝑖 is the angle of incidence of an incident ray, then the ray will be able to propagate if
𝑨𝒄𝒄𝒆𝒑𝒕𝒂𝒏𝒄𝒆 𝒂𝒏𝒈𝒍𝒆 :The maximum angle 𝜽𝒐 is called the acceptance angle , it is defined as
the maximum angle that a light ray can have relative to the axis of the fiber and propagate
through the fiber.
√𝑛12 −𝑛22
ie: NA = 𝑠𝑖𝑛 𝜃𝑜 = 𝑛𝑜
Q: What is meant by numerical aperture(NA) and mention the expression for it.
Numerical aperture is the ability of the optical fiber to accept the light and guide
along the fiber and is numerically equal to sine of the acceptance angle.
√𝑛12 −𝑛22
ie: NA = 𝑠𝑖𝑛 𝜃𝑜 = 𝑛𝑜
[𝑙𝑜𝑔𝑃]𝑃𝑃𝑜𝑖 = −𝛼[𝐿]𝐿0
𝟏𝟎 𝑷
∴ 𝜶 =− log( 𝑷𝒐 ) dB/km
𝑳 𝒊
𝜶𝑳
𝑷𝒐
Note: = 𝟏𝟎−𝟏𝟎
𝑷𝒊
Q: What is V-Parameter/number ?
V-Parameter/number is the quantity which represent the number of modes of the fibre
𝜋𝑑 𝜋𝑑 √𝑛1 2 −𝑛2 2
given by V = . NA = .
𝜆 𝜆 𝑛0
where d = diameter , λ = wavelength,
𝑛1 , 𝑛2 &𝑛0 RI’s of Core, Cladding & medium
Q:What is meant by modes of propagation.
The paths along which the light is guided in the fiber are called modes of
𝑉2
propagation and the number of modes of the fiber is given by N = 2
Cladding
Core
Cladding
Core
Input output
Index profile Cross section profile Modes profile
Cladding
Core
Input
Information Coder Optical
Audio-video Optical fibre REPEATER
receiver AES BES transmitter
carrier
Signal AVS AES Modulator BES OS
[ Receiver
Cum
Transmitter ]
Output
Information De-Coder Optical
Audio-video Optical fibre
transmitter BES AES receiver
Signal carrier
AES AVS De- modulator OS BES
1. Wide bandwidth-the bandwidth of OFCS is very large about 105 GHz compared
to cable communication band width 500MHz.
2. Electrical isolation- OFCS cables are electrically isolated as the optical fibers are
made of insulating glass and plastics.
3. No cross talk- OFCS works on the principle of total internal reflection as there is
no leakage of signal.
4. Economical ,light weight,strong,flexible & small size- optical fibers used in OFCS
are cheap, light weight and small size compared to conventional system.
5. Immune to electro-magnetic interference- Electrically neutral light signals in
OFCS are unaffected by external electromagnetic waves due to
current/magnetic field/lightning/electrical sparks.
6. High signal security- In OFCS the signals transmitted are highly secured as the
leakage can be easily detectable.
7. Low attenuation / transmission loss-In OFCS the transmission loss of the signal
is about 0.2dB/km.
PROBLEMS ON LASERS
𝑛𝜆 𝑁2 ℎ𝐶
Formulae needed: L = ; = 𝑒 −(ℎ𝐶/𝜆𝑘𝑇) ; E= P.t and E =n. ;
2 𝑁1 𝜆
1. Find the number of modes of standing waves in the resonator cavity of length 1 m in
He-Ne temperature of laser operating at wavelength 632.8nm.
Given: L= 1 m ; λ = 632.8 nm = 632.8𝑥10−9 m. n = ?
𝑛𝜆 2𝐿
Using L = ,we get n =
2 𝜆
2𝑥1
=
632.8𝑥10−9
= 3.161 x 106 𝑚𝑜𝑑𝑒𝑠
2. Find the ratio of populations of two energy levels in a laser if the transition between
them produces light of wavelength 6493Å,assuming the ambient temperature as 27℃.
Given: λ = 6493Å = 6493x10−10 m, t=27℃⇨ T = 273+27 =300K; h=6.63x10−34 Js;
𝑁
k=1.38x10−23 J/K ;C=3x108 m/s ;𝑁2 = ?
1
ℎ𝐶
𝑁2 −( )
Using =𝑒 𝜆𝑘𝑇
𝑁1
6.63𝑥10−34 𝑥3𝑥108
−( )
=𝑒 6493𝑥10−10 𝑥1.38𝑥10−23 𝑥300
= 𝑒 −79.99
= 7.33x10−33
3. A He-Ne gas laser is emitting a laser beam with an average power of 4.5 mW. Find the
number of photons emitted per second by the laser. The wavelength of the emitted
radiation is 6328Å.
Given: P=4.5mW = 4.5x10−3 𝑤 ,t= 1 S , C=3x108 m/s ; h=6.63x10−34 Js,
λ = 6328Å = 6328x10−10 m ; n = ?
ℎ𝐶 𝜆𝑃𝑡
Using E= Pxt and E =n. ⇨𝑛 =
𝜆 ℎ𝐶
−10
6328𝑥 10 𝑥4.5𝑥10−3 𝑥1
=
6.63𝑥10−34 𝑥3𝑥108
= 1.432x1016 photons.
4. Find the number of modes of standing waves and their frequency separation in the
resonant cavity of 1 m length of He-Ne operating at wavelength of 632.8 nm.
Given: L= 1 m ; λ = 632.8 nm = 632.8𝑥10−9 m. n = ? and
𝑛𝜆 2𝐿
Using L = , we get , n =
2 𝜆
2𝑥1
=
632.8𝑥10−9
= 3.161 𝑥 106 𝑚𝑜𝑑𝑒𝑠
5. The ratio of population of two energy states in a laser 1.059 x10−30 .If the temperature of
the system is 57°𝐶, 𝑤ℎ𝑎𝑡 𝑖𝑠 𝑡ℎ𝑒 𝑤𝑎𝑣𝑒𝑙𝑒𝑛𝑔𝑡ℎ 𝑜𝑓 𝑡ℎ𝑒 𝑙𝑎𝑠𝑒𝑟 ?
𝑁
Given: 𝑁2 = 1.059x10−30, t = 57°𝐶, ⇨ T =273+57=330K; h=6.63x10−34 Js; k=1.38x10−23
1
𝑁2
λ = −(ℎ𝐶/𝐼𝑛 (𝑁 ) 𝑘𝑇)
1
−6.63𝑥10−34 𝑥3𝑥108
=
𝐼𝑛(1.059𝑥10−30 ) 𝑥1.38𝑥10−23 𝑥330
= 6.328x10−7 𝑚
6. Calculate on the basis of Einstein’s theory the number of photons emitted per second by
He-Ne laser source emitting light of wavelength 6328Å with an optical power 10mW.
Given: P=10mW = 10x10−3 𝑤 ,t=1 s , C=3x108 m/s ; h=6.63x10−34 Js, ,
7. A 5W pulsed laser emits light of wavelength 694 nm. If the duration of each pulse is
20 ns, calculate the number of photons emitted per pulse.
8. The ratio of population of two energy levels out of which one corresponds to metastable
state is 1.059 x10−[Link] 𝑡ℎ𝑒 𝑤𝑎𝑣𝑒𝑙𝑒𝑛𝑔𝑡ℎ 𝑜𝑓 𝑙𝑖𝑔ℎ𝑡 𝑒𝑚𝑖𝑡𝑡𝑒𝑑 𝑎𝑡 330𝐾.
𝑁
Given: 𝑁2 = 1.059x10−30 , T =330K; h=6.63x10−34 Js; k=1.38x10−23 J/K ;
1
C=3x108 m/s ; λ = ?
𝑁2
Using = 𝑒 −(ℎ𝐶/𝜆𝑘𝑇)
𝑁1
𝑁2 𝑁
we get , In( ) = −(ℎ𝐶/𝜆𝑘𝑇) 𝑆𝑖𝑛𝑐𝑒: 𝑙𝑜𝑔𝑒 (𝑁2 ) = In(𝑁𝑁2)
𝑁1 1 1
𝑁2
λ = −(ℎ𝐶/𝐼𝑛 (𝑁 ) 𝑘𝑇)
1
−6.63𝑥10−34 𝑥3𝑥108
=
𝐼𝑛(1.059𝑥10−30 ) 𝑥1.38𝑥10−23 𝑥330
= 6.328x10−7 𝑚
ℎ𝐶
Using E= Pxt and E =n.
𝜆
𝜆𝑃𝑡
We get, 𝑛=
ℎ𝐶
6500 𝑥 10−10 𝑥10𝑥10−3 𝑥1
=
6.63𝑥10−34 𝑥3𝑥108
=3.268 x 1016 𝑝ℎ𝑜𝑡𝑜𝑛𝑠/𝑚3
[Link] the ratio of population of two energy levels in a medium at thermal equilibrium ,
if the wavelength of light emitted at 291 K is 6928 Å .
= 𝑒 −71.44
= 9.419x10−32 or = 9.441x10−32
6.63𝑥10−34 𝑥 3𝑥108
−( )
=𝑒 1𝑥10−6 𝑥1.38𝑥10−23 𝑥300
= 𝑒 −48.044
= 1.364 x10−21
13. A laser operating at 632.8nm emits 3.182 x 1016 photons per second. Calculate the output
power of the laser if the input power is 100 watt. Also find the percentage power converted
into coherent light energy. ( 4 Marks)
ℎ𝐶
Using E= 𝑃𝑜 xt and E =n.
𝜆
𝑛ℎ𝐶
We get, 𝑃𝑜 =
𝜆𝑡
3.182 𝑥 1016 𝑥6.625𝑥10−34 𝑥3 𝑥 10
=
632.8 𝑥 10−9 𝑥1
= 9.99x10−3 W
𝑃𝑜
Fraction of input power converted to light = 𝑥100
𝑃𝑖
9.99𝑥10−3
𝑥100 = 9.99x10−3 % = 0.001 %
100
−𝛼𝐿
𝑛𝜆 10 𝑃𝑜
Formulae needed: L = ;𝛼 =− log[ ] ; 𝑃𝑜 = 𝑃𝑖 10 10 ;
2 𝐿 𝑃𝑖
√𝑛1 2 −𝑛2 2 𝜋𝑑 𝑉2 (𝑛1 −𝑛2 )
NA = ; Sin𝜃𝑜 = NA ; V = X NA ; N = ;∆=
𝑛𝑜 𝜆 2 𝑛1
1. Find the number of modes of standing waves in the resonator cavity of length 1 m in He-
Ne temperature of laser operating at wavelength 632.8nm.
Given: L= 1 m ; λ = 632.8 nm = 632.8𝑥10−9 m. n = ?
𝑛𝜆 2𝐿
Using L = ,we get n =
2 𝜆
2𝑥1
=
632.8𝑥10−9
= 3.161 x 106 𝑚𝑜𝑑𝑒𝑠
2. A fiber with an input power of 9μW has a loss of 1.5 dB/km. If the fiber is 3000 m long,
calculate the output power.
−6
𝑤 = 3019 𝑥 10
3. The numerical aperture of an optical fibre is 0.2 when surrounded by air. Determine the
R.I of its core, given the R.I of the cladding is [Link] find the acceptance angle when the
fibre is in water of R.I 1.33.
Given: 𝑛𝑜 𝑥 NA = 0.2 , 𝑛2 = 1.59 , 𝑛′𝑜 = 1.33 , 𝑛1 =? a𝑛𝑑 𝜃′𝑜 = ?
√𝑛1 2 −𝑛2 2
For air , Using NA = , we get 𝑛1 = √(𝑛𝑜 𝑥𝑁𝐴)2 + 𝑛22
𝑛𝑜
= √( 0.22 + 1.592 )
= 1.603
√𝑛1 2 −𝑛2 2 √1.6032 −1,592
Also 𝜃 ′ 𝑜 = 𝑆𝑖𝑛−1( ) = 𝑆𝑖𝑛−1 ( ) = 8.65°
𝑛′ 𝑜 1.33
4. The angle of acceptance of an optical fibre is 30° 𝑤ℎ𝑒𝑛 kept in air. Find the angle of
acceptance when it is in a medium of refractive index 1.33.
Given: 𝜃𝑜 =30° , 𝑛′𝑜 =4/3=1.333 , 𝑛𝑜 = 1 𝑓𝑜𝑟 𝑎𝑖𝑟 , 𝜃′𝑜 =?
Using 𝑛′𝑜 𝑆𝑖𝑛 𝜃′𝑜 = 𝑛𝑜 Sin𝜃𝑜 = √𝑛1 2 − 𝑛2 2 = constsnt
We get , 𝜃′𝑜 = 𝑆𝑖𝑛−1 (𝑛𝑜 𝑆𝑖𝑛𝜃𝑜 ⁄𝑛′𝑜 )
= 𝑆𝑖𝑛−1 (1 𝑆𝑖𝑛30°⁄1.333)
=22.03°
5. Calculate the NA,V-number and number of modes in an optical fibre of core diameter
50μm,core and cladding refractive indices 1.41 and 1.4 at wavelength 820 nm.
Given: 𝑛1 = 1.41 ; 𝑛2 = 1.4 ; λ = 820 nm= 820 x 10−9 m ; d = 50μm =50x 10−6 m ;
𝑛𝑜 =1 for air NA = ? ; V = ? & N = ?
√𝑛1 2 −𝑛2 2 √(1.41)2 −(1.4)2
a. NA = = =0 .168
𝑛𝑜 1
𝑉2 (32.17)2
c. N= = = 517.5 = 518
2 2
6. The refractive indices of the core and cladding of a step index fibre are 1.45 and 1.40
respectively and its core diameter is 45μ[Link] its relative refractive index
difference, V- number at wavelength 1000 nm and number of modes.
Given: 𝑛1 = 1.45 ; 𝑛2 = 1.4 ; λ = 1000 nm= 1000 x 10−9 m ; d = 45μm =45x 10−6 m ; 𝑛𝑜 = 1; ∆ = ? ;
V=?&N=?
(𝑛1 −𝑛2 ) (1.45−1.4)
1) ∆ = = = 0.0345
𝑛1 1.45
𝜋𝑑 √𝒏𝟏 𝟐 −𝒏𝟐 𝟐 3.14𝑥45𝑥 10−6 𝑥√1.452 −1.4 2
2) V = 𝑋 = = 53.34
𝜆 𝒏𝒐 1000 𝑥 10−9 𝑥1
𝑉2 (53.34)2
3) N= = = 1422.6 =1423
2 2
7. Find the number of modes of standing waves and their frequency separation in the
resonant cavity of 1 m length of He-Ne operating at wavelength of 632.8 nm.
8. A signal with input power 200mW loses 10% of its power after travelling a distance of
3000 m. Find the attenuation coefficient of the fiber.
9. An optical fiber has core R.I 1.5 and R.I of cladding is 3% less than the core index. Calculate
the numerical aperture, angle of acceptance and internal critical acceptance angle.
1.455
𝑛2 𝑛 −1( )
3) 𝑠𝑖𝑛 𝜃𝐶 = ⇨ 𝜃𝐶 = 𝑆𝑖𝑛−1 ( 2) = 𝑆𝑖𝑛 1.5 = 75.93°
𝑛1 𝑛1
10. The angle of acceptance of an optical fiber kept in air is 30°.Find the angle of acceptance
when the fiber is in a medium of refractive index 4/3.
12. An optical signal propagating in a fiber retains 85% of input power after
travelling a distance of 500 m in the fiber. Calculate the attenuation coefficient.
Given: 𝑃𝑜 = 85% 𝑃𝑖 = 0.85 𝑃𝑖 ; L = 500m = 0.5 km; 𝛼 =? ,
10 𝑃
Using 𝛼 =− log[ 𝑜 ]
𝐿 𝑃𝑖
10 0.85 𝑃𝑖 10
=− log [ ] = − log [0.85]
0.5 𝑃𝑖 0.5
= 1.412 dB/km
13. The attenuation of light in an optical fiber is 2 dB/km. What fraction of its
intensity remains after (i) 2 km, (ii) 5 km ?
𝑑𝐵 𝑃 𝑃
Given: 𝛼 = 2 𝑘𝑚, ( 𝑃𝑜 ) =?, ( 𝑃𝑜 ) =?
𝑖 𝐿=2𝑘𝑚 𝑖 𝐿=5𝑘𝑚
−𝛼𝐿
𝑃
Using ( 𝑃𝑜 ) = 10 10
𝑖 𝐿
−𝛼𝐿 −2𝑥2
𝑃
(𝑃𝑜 ) = 10 10 = 10 10 = 0.3981
𝑖 𝐿=2𝑘𝑚
−𝛼𝐿 −2𝑥5
𝑃
( 𝑃𝑜 ) = 10 10 = 10 10 = 0.1
𝑖 𝐿=5𝑘𝑚
14. The refractive indices of the core and cladding of a step-index optical fibre
are 1.45 and 1.40 respectively and its core diameter is 45μm. Calculate its
fractional refractive index change and numerical aperture.
Given: 𝑛1 = 1.45 ; 𝑛2 = 1.4 ; ; d = 45μm =45x 10−6 m ; ∆ = ? ; & NA = ?
(𝑛1 −𝑛2 ) (1.45−1.4)
1) ∆ = = = 0.0345
𝑛1 1.45
√𝒏𝟏 𝟐 −𝒏𝟐 𝟐 √1.452 −1.42
2) NA = 𝒏𝒐
= 1
= 0.3775
15. Calculate the numerical aperture and angle of acceptance for an optical fibe
having refractive indices 1.563 and 1.498 for core and cladding respectively.
[Link] a slab waveguide made of AlGaAs having RI for core and clad 3.6 and 3.55
respectively. Find how many modes can propagate in this waveguide if d = 5 ( 4 Marks)
Given: 𝑛1 = 3.6 ; 𝑛2 = 3.55 ; d = 5λ =45x 10−6 m ; 𝑛𝑜 1; ∆ = ? ; V = ? & N = ?
MODULE-4
Blow up syllabus
5.1 Quantum free electron theory: Review of classical free electron theory (Just mention who No numerical problems
proposed it and what for it was proposed), mention the expressions for electrical conductivity
based on classical free electron theory, and explain the failures of classical free electron theory
(in terms of relation between conductivity and temperature, and relation between conductivity
and free electron density, with specific examples)
Assumptions of quantum free electron theory, definition of density of states and mention the Numerical
expression for density of states (No derivation) problems
Qualitative discussion of Fermi level, Fermi energy, Fermi-Dirac statistics, Fermi factor, Fermi Numerical
factor at different temperatures Fermi factor (3 cases). problems
Derivation of the expression for Fermi energy at zero Kelvin. Mention the expression Fermi Numerical
velocity and Fermi temperature. Expression for electrical conductivity in terms of problems
velocity, mean free path and effective mass [No derivation).
/'
Success of quantum free electron theory (in terms of relation between conductivity and No numerical problems
temperature, and relation between ~ conductivity and free electron density, with specific
examples)
5.2 Semiconductors: Fundamentals of semiconductor. Description of Fermi level in
I No numerical problems
intrinsic semiconductor. Mention of expression for electron and hole concentration in intrinsic
semiconductors. Derivation of relation between Fermi energy and energy gap for an intrinsic
semiconductor.
Derivation of the expression for electrical .conductivity of semiconductors, Explanation of Hall Numerical
effect with Hall voltage and Hall field, derivation of the expression for Hall coefficient. problems
5.3 Dielectrics: Fundamentals of dielectrics. Polarisation, mention the relation No numerical problems
between dielectric constant and polarization. Types of polarization. Polar and non-polar
dielectrics
Definition of internal field in case of solids and mention of its expression for one dimensional Numerical
case. Mention the expressions for internal field for three dimensional cases and Lorentz field. problems
internal field andDerivation of Clausius-Mossotti equation
Description of solid, liquid and gaseous dielectrics with one example each. Qualitative No numerical problems
explanation of applications of dielectrics in transformers.
Tutorial classes , ~ Involvement of students in respect of their doubts about the
module and numerical problems
Module-4
1. CFET and its failures.
2. Assumptions of QFET ,Success of QFET – relations between 𝝈 & 𝑇 , 𝝈 & 𝑛
3. Define Fermi energy, explain variation of Fermi factor with temperature.
4. Derive the expression for Fermi energy at 0k.
5. Derivation of relation between Fermi energy and Energy gap for an intrinsic semiconductor.
6. Derivation of an expression for electrical conductivity of semiconductor.
7. Derivation of an expression for Hall coefficient, express Hall voltage interms of Hall coefficient.
8. Relation between dielectric constant and Polarization, types of polarization and Polar and non-
polar dielectrics.
9. Internal field in solid dielectrics with one dimensional equation.
10. Derivation of Clausius- Mosotti equation.
11. Types of dielectrics -Solids, Liquids & gases with one example each. Qualitative explanation of
I/II SEM application of dielectric in Transformers. Page 67
RAMESH R 21PHY12/22
MODULE-4
Concept of free electrons:
All the metals consists of atoms, the outermost electrons of these atoms are called
Valance electrons. These valance electrons are weakly bound to their atoms where as they
are freely moving within the body of the metal. These electrons are responsible for
number of properties of metals like electrical conductivity, thermal conductivity and these
electrons are called as conduction electrons.
Classical free electron theory(CFET)/ Drude-Lorentz theory.
CFET is a theoretical model given by [Link] and Lorentz to explain some of the
outstanding properties of metals.
Assumptions:
1. All the metals consists of free moving valance electrons called free electrons. When E.F
is applied these electrons move opposite to the direction of applied field.
2. The free electrons are treated equivalent to gas molecules and thus obey laws of
3 2 1
kinetic theory of gases. i.e., 2 kT =2 m𝑣𝑡ℎ
3. The electrical potential due to ionic cores is taken to be essentially constant
throughout the metal.
4. The attraction between electrons and lattice ions, and repulsion between electrons
themselves are considered insignificant.
Mean free path and Mean collision time:
When E.F is not applied to a metal, the free electrons are randomly moving and they are
colliding with lattice ions.
“ The average distance travelled by conduction electrons between two successive collisions
is called Mean free path (𝝀)".
“ The average time elapsed between two successive collisions is called mean collision
time(𝝉).
Drift velocity: The average velocity with which all free electrons drifts in the direction
opposite to that of applied E.F in a metal is called Drift velocity.
−𝒆𝝉𝑬
∴ 𝒗𝒅 =
𝒎
Mobility(μ) of electrons is defined as the drift velocity (𝒗𝒅 )acquired by the electrons per unit
𝒗𝒅 𝝈 𝒆𝝉
electric field(E). ie: μ = ⇨μ= ⇨μ=
𝑬 𝒏𝒆 𝒎
Q:Expression for electrical conductivity and hence electrical resistivity from CFET.
𝒏𝒆𝟐 𝝉
Electrical conductivity, 𝝈 = where n= concentration of electrons, e= charge on
𝒎
electron,𝜏 = mean collision time, m= mass of the electron.
1
Also, Electrical resistivity, 𝜌 =
𝜎
𝒎
∴ 𝝆=
𝒏𝒆𝟐 𝝉
𝑛𝑒 2 𝜏
𝐹𝑟𝑜𝑚 𝜎 = , we get 𝜎 ∝ 𝑛 , according to CFET 𝝈 𝑜𝑓 tri-atomic metals must be more
𝑚
than that of di-atomic and mono-atomic metals but from experimental results as shown in
the tabular column, it has been found that 𝝈 of mono-atomic metals of low n are more than
that of di and tri-atomic metals of large n .Thus CFET fail to explain dependence of 𝝈 on
concentration n.
Q:State/Mention the assumptions of (Somerfield’s)quantum free electron theory(QFET)
The assumptions of QFET are:
[Link] energy of free electrons are quantized.
2. Free electrons obey Pauli’s exclusion principle.
3. The distribution of free electrons in energy levels is governed by Fermi-Dirac
statistics.
4. Free electrons move in uniform potential field due to ionic cores in a metal .
5. The electrostatic electron-ion attractions and electron-electron repulsions
are negligible.
Q:What is meant by Density of states ? Explain.
Density of states g(E) is defined as the number of electronic states present in a unit energy
𝟖√𝟐𝝅𝒎𝟑/𝟐
range ,given by, g(E) 𝒅𝑬 = 𝑬𝟏/𝟐 𝒅𝑬. It is a continuous function and the
𝒉𝟑
product g(E)dE=dN gives the number of states per unit volume in an energy range
(dE)between E and E+dE The number of electrons per unit volume , n= ∫ 𝑔(𝐸)𝑓(𝐸)𝑑𝐸 and
the variation of g(E) with E is shown in the graph.
g(E)
0
E
Fermi energy(𝑬𝑭 ): is defined as the energy of the highest occupied Fermi level in a metal at 0K.
(or)
“Fermi energy is the highest energy possessed by an electron at zero Kelvin and
corresponding level is Fermi level”. Therefore at absolute zero, all the energy levels
above Fermi level are empty and that of below are completely filled.
Q:What is meant by Fermi factor ?Explain the variation of Fermi factor with temperature & energy.
Fermi factor is the probability of occupation of a given energy state by an electron in a metal
𝟏
at thermal equilibrium. It is given by the relation f(E) = (𝑬−𝑬 ,where 𝐸𝐹 𝐹𝑒𝑟𝑚𝑖 𝑒𝑛𝑒𝑟𝑔𝑦,
𝟏+𝒆 𝑭 )/𝒌𝑻
E = energy of State, k = Boltzmann constant and T = temperature
The variation of f(E) with temperature and energy is discussed below:
When T = 0K
Case-1: If E < 𝐸𝐹 ⇨ (𝑬 − 𝑬𝑭 )𝑖𝑠 − 𝑣𝑒 ,then 𝒆(𝑬−𝑬𝑭)/𝒌𝑻 = 𝒆−∞ = 0
𝟏 𝟏
∴ f(E) = = =1,
𝟏+𝒆(𝑬−𝑬𝑭)/𝒌𝑻 𝟏+𝟎
Thus the probability of occupation up to Fermi level is 100%.
Case-2: If E > 𝐸𝐹 ⇨ (𝑬 − 𝑬𝑭 )𝑖𝑠 + 𝑣𝑒 ,then 𝒆(𝑬−𝑬𝑭)/𝒌𝑻 = 𝒆∞ = ∞
𝟏 𝟏 1
∴ f(E) = = = =0,
𝟏+𝒆(𝑬−𝑬𝑭)/𝒌𝑻 𝟏+∞ ∞
𝟎
Case-3: If E = 𝐸𝐹 ⇨ (𝑬 − 𝑬𝑭 ) = 0 ,then 𝒆(𝑬−𝑬𝑭)/𝒌𝑻 = 𝒆𝟎 indeterminate.
f(E) Note: 𝑇1 = 500𝑘 < 𝑇2 =1000k
When T > 0K
𝟏
∴ f(E)=
𝟏+𝒆(𝑬−𝑬𝑭)/𝒌𝑻
1 T = 0K
Fermi velocity(𝒗𝑭 ): of an electron is defined as it’s velocity when it’s energy is equal to
1 𝟐𝑬
the Fermi energy. ie: 𝑚𝑣𝐹2 = 𝐸𝐹 ⇨𝒗𝑭 = (√ 𝒎𝑭 )
2
𝐸 8√2𝜋𝑚3/2
n = ∫0 𝐹0 𝐸1/2 𝑑𝐸
ℎ3
8√2𝜋𝑚3/2 𝐸𝐹0
= ∫0 𝐸1/2
ℎ3
8√2𝜋𝑚3/2 2 𝐸𝐹0
= [3 𝐸 3/2 ]
ℎ3 0
8√2𝜋𝑚3/2 2 3/2
= (𝐸𝐹0 )
ℎ3 3
3/2 ℎ3 3𝑛
(𝐸𝐹0 ) = 3/2
( )
(8𝑚) 𝜋
𝒉𝟐 𝟑 𝟐/𝟑
𝑬𝑭𝟎 = 𝟖𝒎 ( 𝝅 ) 𝒏𝟐/𝟑 or 𝑬𝑭𝟎 = 5.85 x𝟏𝟎−𝟑𝟖 𝒏𝟐/𝟑
PROBLEMS
1 𝑚 1 𝑛𝑒 2 𝜏
Formulae needed : f(E) = 𝐸−𝐸𝐹 ; 𝜌 = ; 𝜎= ;𝜎 = ;
𝑛𝑒 2 𝜏 𝜌 𝑚
1+𝑒 𝑘𝑇
𝑥𝐷𝑁𝐴 1 𝑒𝐸𝜏 𝜎 1
n= ;𝜇 = ;½ m𝑉𝐹 2 = 𝐸𝐹 ; 𝑉𝑑 = ; λ = 𝑉. 𝜏 ; n = =
𝑀 𝑛𝑒𝜌 𝑚 𝜇𝑒 𝜌𝜇𝑒
1. Find the relaxation time of conduction electrons in a metal of resistivity 1.54 x10−8 Ω-m, if
the metal has 5.8 x1028 Conduction electrons per 𝑚3 .
3. Find the temperature at which there is 1.0% probability that a state with an energy 0.5eV
above Fermi energy will be occupied.
𝑛𝑒 2 𝜏
Also, 𝜎 =
𝑚
2.54𝑥1028 𝑥( 1.6𝑥10−19 )2 𝑥2 𝑥 10−14
=
9.1𝑥10−31
= 1.42x107 Ωm.
5. Calculate the Fermi velocity and the mean free path for the conduction electrons in silver,
given that its Fermi energy is 5.5 eV and relaxation time for electrons is 3.97 X10−14S.
2𝑥5.5 𝑥 1.6𝑥10−19
=√
9.1𝑥10−31
= 1.391x 106 m/s and
Also, λ =𝑉𝐹 . 𝜏𝑟 = 1.391x 106 x 3.97 X10−14 = 5.522𝑥 10−8 m
6. The Fermi level of potassium is 2.1eV. What are the energies for which the probabilities of
occupancy at 300 K are 0.99 and 0.5 ?
1
Also, 𝐸2 = 2.1𝑥1.6𝑥10−19 + 1.38x10−23 𝑥300 𝐼𝑛 [ 0.5 – 1]
= 3.36 𝑥10−19 −0
−19
= 3.36 𝑥10 𝐽
3.36 𝑥10−19
= eV
1.6 𝑥10−19
= 2.1 eV
7. The Fermi level for a metal is 2.1eV, calculate the energies for which the probability of
occupancy at 300 K are 98% and 50%.
1
Using f(E)= ,
1+𝑒 (𝐸−𝐸𝐹 )/𝑘𝑇
1
we get E = 𝐸𝐹 + 𝑘𝑇 𝐼𝑛 [ 𝑓(𝐸) – 1]
1
∴ 𝐸1 = 2.1𝑥1.6𝑥10−19 + 1.38x10−23 𝑥300 𝐼𝑛 [ 0.98 – 1]
= 3.36 𝑥10−19 − 0.16 𝑥10−19
= 3.2x10−19 𝐽
3.2𝑥10−19
= eV
1.6𝑥10−19
=2eV
1
Also , 𝐸2 = 2.1𝑥1.6𝑥10−19 + 1.38x10−23 𝑥300 𝐼𝑛 [ 0.5 – 1]
= 2.1𝑥1.6𝑥10−19 −0
−19
2.1𝑥1.6𝑥10
= eV
1.6𝑥10−19
= 2.1 eV
8. A uniform silver wire has resistivity 1.54 x10−8 𝛺𝑚 at room temperature for an electric
field 2 V/m. Calculate relaxation time and drift velocity of the electrons, assuming that
there are 5.8 X 1022 conduction electrons per 𝑐𝑚3 of the material.
Given: 𝜌 = 1.54 x 10−8 Ω-m ; E = 2 V/m ; 𝑛 = 5.8 𝑋 1022 /𝑐𝑚3 = 5.8 𝑋 1022 𝑥10−6 /
𝑚3 ; 𝑚 = 9.1𝑥10−31 𝑘𝑔 ; 𝑒 = 1.6𝑥10−19 𝐶 ; 𝜏 = ? & 𝑉𝑑 = ?
𝜌𝑚
𝑈𝑠𝑖𝑛𝑔: 𝜏 =
𝑛𝑒 2
1.54 𝑥 10−8 𝑥9.1𝑥10−31
=
5.8 𝑋 1022 𝑥10−6 ( 1.6𝑥10−19 )2
= 9.44 x10−18 S
𝑒𝐸𝜏
𝑉𝑑 =
𝑚
1.6𝑥10−19 𝑥2𝑥9.44 𝑥10−18
=
9.1𝑥10−31
= 3.32 x 10−6 m/s
9. Calculate the probability of an electron occupying an energy level 0.02 eV above the Fermi
level at 300K.
1
Using f(E) =
1+𝑒 (𝐸−𝐸𝐹 )/𝑘𝑇
1
= −19 )/1.38𝑥10−23 𝑥 300
1+𝑒 (0.02𝑥1.6𝑥10
1
=
1+𝑒 0.773
1
=
1+2.166
1
=
3.166
=0.32 or 32 %
10. Calculate the concentration at which the acceptor atoms must be added to a germanium
sample to get a P-type semiconductor with conductivity 0.15 per Ohm-metre. Given the
mobility of holes=0.17 𝑚2 /Vs.
𝜎
Using, n =
𝜇𝑒
0.15
=
0.17𝑥1.6𝑥10−19
= 5.515 x1018 electrons
11. Calculate the mobility of electrons in copper assuming that each atom
Contribute one free electron for conduction. Resistivity of copper=1.7 X 10−8
Ωm, atomic weight =63.54,density =8.96 X 103 kg/𝑚3 ( CBCS-Jun/Jul16)
Given: 𝜌 = 1.7 x 10−8 Ω-m ; M = 63.54 ; D = 8.96 x 103 kg/𝑚3 ; 𝑁𝐴 =6.025 x 1026 /kg mole
; 𝑚 = 9.11𝑥10−31 𝑘𝑔 ; 𝑒 = 1.6𝑥10−19 𝐶 ; 𝑥 = 1𝑒𝑙𝑒𝑐𝑡𝑟𝑜𝑛/𝑎𝑡𝑜𝑚, 𝑛 = ? ; 𝜇 = ?
𝑥𝐷.𝑁𝐴
𝑈𝑠𝑖𝑛𝑔 n =
𝑀
1𝑥8.96 𝑥 103 𝑥.6.025 𝑥 1026
=
63.54
28
= 8.5x10 atoms.
1
𝜇=
𝑛𝑒𝜌
1
= = 4.325x10−3 𝑚2 /vs
8.5𝑥1028 𝑥1.6𝑥10−19 𝑥1.7 𝑥 10−8
12. For intrinsic gallium arsenide, the room temperature electrical conductivity is
10−6 /Ω[Link] electron and hole mobilities are respectively 0.85 𝑚2 /𝑉𝑠 and
0.04 𝑚2 /𝑉𝑠. 𝐶alculate the intrinsic carrier concentration at room temperature.
𝐸𝑔 0.66
𝐸𝐹 = = = 0.33 𝑒v
2 2
𝜋𝑚∗𝑒 𝑘𝑇 3/2
𝐸 −𝐸𝑔
( 𝐹 )
Using ; 𝑛𝑒 = 4√2 ( 2 ) 𝑒 𝑘𝑇
ℎ
(0.33−0.66)𝑥1.6𝑥10−19 )
𝜋𝑥0.55𝑥 9.1 𝑥 10−31 𝑥1.38𝑥10−23 𝑥300 3/2
= 4√2 ( ) x𝑒 1.38𝑥10−23 𝑥300
(6.625𝑥10−34 )2
= 5.657x1.807x1024 x2.892x10−6
𝑛𝑒 = 2.956x1019 /𝑚3
14. For intrinsic Gallium Arsenide , the electric conductivity at room temperature
is 10−6 𝑜ℎ𝑚−1 𝑚−1 . The electron and hole mobilities are respectively 0.85 𝑚2 /𝑉𝑆 𝑎𝑛𝑑
0.04 𝑚2 /𝑉𝑆. Calculate the intrinsic carrier concentration at room temperature.
1
Using f(E) =
1+𝑒 (𝐸−𝐸𝐹 )/𝑘𝑇
1
= −19 )/1.38𝑥10−23 𝑥 200
1+𝑒 (0.02𝑥1.602𝑥10
1
=
1+𝑒 1.161
1
=
1+3.193
1
=
4.193
= 0.2385 or 23.85 %
16. Gold has one free electron/[Link] density,atomic weight and resistivity are
19300 kg/𝑚3 ,197 and 2.21 x 10−8 Ω𝑚 . Calculate the free electron concentration
and mobility of conduction electron.
Given : D=19300 kg/𝑚3 , M =197 , 𝜌 = 2.21 x 10−8 Ω𝑚 , 𝑥 = 1 electron/atom,
𝑁𝐴 = 6.02 x 1028 /Kmol , e=1.6 x 10−19 C , n =? , 𝜇 = ?
𝑥 𝐷 𝑁𝐴
Using, n = 𝑀
18. The electron concentration in a semiconductor is 5 x 1017 𝑚−3 . Calculate the conductivity
of the material if the drift velocity of electron is 350 m𝑠 −1 in an electric field of 1000 V𝑚−1 .
Given: 𝑛 =5 x 1017 𝑚−3, 𝑉𝑑 = 350 m𝑠 −1, 𝐸 = 1000 V𝑚−1. 𝜎 =?
𝑛𝑒 2 𝜏 𝑒𝐸𝜏
Using 𝜎 = and 𝑉𝑑 =
𝑚 𝑚
𝑛𝑒𝑉𝑑 5 𝑥 10 𝑥1.6𝑥10−19 𝑥350
17
We get 𝜎 = = =0.028/Ωm.
𝐸 1000
19. Calculate the Fermi velocity and the mean free path for the conduction electrons
in silver, given that its Fermi energy is 5.5V and the relaxation time for electrons
is 3.83 x 10−14 S.
Given: 𝐸𝐹 = 5.5 𝑒𝑉 = 5.5 𝑥 1.6𝑥10−19 𝐽 ; 𝜏 = 𝜏𝑟 = 3.83 X10−14 S ; 𝑚 = 9.1𝑥10−31 𝑘𝑔 𝑉𝐹 = ? :
λ=?
2𝐸𝐹
Using ½ m𝑉𝐹 2 = 𝐸𝐹 ,we get 𝑉𝐹 = √
𝑚
2𝑥5.5 𝑥 1.6𝑥10−19
=√
9.1𝑥10−31
= 1.391x 106 m/s and
Also, λ =𝑉𝐹 . 𝜏𝑟 = 1.391x 106 x 3.83 X10−14 = 5.328𝑥 10−8 m
PHYSICS OF SEMICONDUCTORS
Semiconductors have conductivity in the range intermediate between those of good
conductors and insulators. Elements such as Silicon, Germanium are the examples of
semiconductors.
Q: Mention of expression for electron & hole concentration in an intrinsic
semiconductor.
We know that the number of energy levels between the energy interval E and E+dE
8√2𝜋(𝑚𝑒∗ )3/2
is given by g(E)dE = (
ℎ3
) 𝐸1/2 𝑑𝐸 ,where 𝑚𝑒∗ = effective mass of
electron. Also, the probability of occupation of an energy level is given by Fermi factor
1
f(E) = 𝐸−𝐸𝐹 where 𝐸𝐹 = 𝐹𝑒𝑟𝑚𝑖 𝑒𝑛𝑒𝑟𝑔𝑦 & 𝑘 = 𝐵𝑜𝑙𝑡𝑧𝑚𝑎𝑛𝑛 𝑐𝑜𝑛𝑠𝑡𝑎𝑛𝑡
( )
1+ 𝑒 𝑘𝑇
𝟑/𝟐 −𝑬𝑭
𝝅𝒎∗𝒉 𝒌𝑻 ( )
𝒏 𝒉 = 𝟒√ 𝟐 ( ) 𝒆 𝒌𝑻
𝒉𝟐
Describe Fermi level in intrinsic semiconductor and hence obtain the expression .
(Or)
Relation between Fermi energy and Energy gap for an intrinsic semiconductor.
At 0K, all the energy levels of valence band are completely filled and all the levels of
conduction band are empty. But at ordinary room temperature and above some of the
electrons from valence excite and fill bottom levels of conduction band. As a result bottom
levels of conduction band and top levels of valence band are filled. Due to this the average
1
energy of the conduction electrons is 2 𝐸𝑔 ,where 𝐸𝑔 is the energy gap.
Thus for an intrinsic semiconductor the Fermi Level lies at the middle of the energy
gap/band.
WKT,
The concentration of electron charge carriers is given by
𝐸 −𝐸𝑔
𝜋𝑚𝑒∗ 𝑘𝑇 3/2 ( 𝐹 )
𝑛𝑒 = 4√2 ( ) 𝑒 𝑘𝑇 ….(1)
ℎ2
∗ 3/2 −𝐸𝐹
𝜋𝑚ℎ 𝑘𝑇 ( )
𝑛ℎ = 4√2 ( ℎ2
) 𝑒 𝑘𝑇 …….(2)
But for an intrinsic semiconductor, 𝑛𝑒 = 𝑛ℎ …….(3)
𝐸 −𝐸𝑔 −𝐸𝐹
( 𝐹 ) ( )
From equations 1,2 &3,we get ( 𝑚∗𝑒 3/2
) 𝑒 𝑘𝑇 =( 𝑚∗ℎ 3/2
) 𝑒 𝑘𝑇
2𝐸𝐹−𝐸𝑔
( ) 𝑚∗ℎ 3/2
𝑒 𝑘𝑇 =( )
𝑚∗𝑒
3 𝑚∗ℎ 𝐸𝑔
𝐸𝐹 = kT ln( ∗
)+
4 𝑚𝑒 2
𝑬𝒈
Practically, 𝑚𝑒∗ = 𝑚ℎ∗ , ln= 0 ∴ 𝑬𝑭 = , Thus ,the Fermi level is in the middle of the band gap
𝟐
for an intrinsic semiconductor.
Hall Effect:
When magnetic field is applied perpendicular to the direction of the current in a conductor,
a potential difference develops along a direction perpendicular to both current and
magnetic field. This effect is known as Hall effect. The potential difference developed is
known as Hall voltage. (Or)
Y 1
d I
0 w X
Z B 2
Consider a rectangular conductor of cross section w x d =a in which current “I” flows along
x-axis. when a magnetic field ‘B’ is applied along z-axis, Hall voltage 𝑉𝐻 develops along y-
axis between the terminals 1&2.
If 𝐸𝐻 be the Hall electric field and ‘ 𝑣 ’be the drift velocity (of charges)
Then under equilibrium conditions,
Force on charges due to Hall electric field = Force on charges due to magnetic field
ie: 𝑞𝐸𝐻 = q 𝑣B
𝑉𝐻
∴ 𝐸𝐻 = 𝑣B also 𝐸𝐻 = 𝑑
𝑉𝐻
∴ = 𝑣B or 𝑉𝐻 = 𝑣Bd ……..(1)
𝑑
𝐼
Wkt, I = nqa𝑣 or 𝑣 = 𝑛𝑞𝑎 …..(2)
𝐼𝐵𝑑
∴ from eqns 1&2 ,we get 𝑉𝐻 = 𝑛𝑞𝑎 but a = w x d
𝐼𝐵
∴ 𝑉𝐻 = 𝑛𝑞𝑤 ……..(3)
1
The quantity 𝑛𝑞 is the reciprocal of charge density and is called the Hall coefficient ‘𝑅𝐻 ’
𝟏
𝑖𝑒; 𝑹𝑯 = 𝒏𝒒 …..(4)
𝑰𝑩
From eqns 3&4 we get 𝑽𝑯 = 𝑹𝑯 ( 𝒘 ) ………(5)
𝑅𝐻 and charge density can be determined as 𝑉𝐻 ,B,d and a are all measurable quantities.
Uses of Hall effect:
[Link] effect is used to find the nature of the charges( Positive or Negative) which in turn determine
whether the semiconductor is N-type or P-type.
2. Hall effect is used to find the density of charge carriers.
[Link] effect is used to find the mobility of charge carriers.
[Link] effect is used to find Hall voltage, Hall angle & Hall coefficient.
[Link] effect sensors work on the principle of Hall effect used to detect/sense magnetic fields
ranging from 1𝜇𝑇 𝑡𝑜 1 𝑇. (𝐸𝑎𝑟𝑡ℎ′ 𝑠 𝑚𝑎𝑔. 𝑓𝑖𝑒𝑙𝑑 50𝜇𝑇)
6. Hall effect device is used as multipliers as Hall voltage is the product of current and
magnetic field.
PROBLEMS ON SEMICONDUCTORS
1. Calculate the Fermi velocity and the mean free path for the conduction electrons in
silver, given that its Fermi energy is 5.5 eV and relaxation time for electrons is 3.97
X10−14 S. (𝐷𝑒𝑐 2011)
2𝑥5.5 𝑥 1.6𝑥10−19
=√
9.1𝑥10−31
= 1.391x 106 m/s and
Also, λ =𝑉𝐹 . 𝜏𝑟 = 1.391x 106 x 3.97 X10−14 = 5.522𝑥 10−8 m
𝜎
Using, n =
𝜇𝑒
0.15
=
0.17𝑥1.6𝑥10−19
= 5.515 x1018 electrons
𝜋𝑚∗𝑒 𝑘𝑇 3/2
𝐸 −𝐸𝑔
( 𝐹 )
Using ; 𝑛𝑒 = 4√2 ( 2 ) 𝑒 𝑘𝑇
ℎ
(0.33−0.66)𝑥1.6𝑥10−19 )
𝜋𝑥0.55𝑥 9.1 𝑥 10−31 𝑥1.38𝑥10−23 𝑥300 3/2
= 4√2 ( ) x𝑒 1.38𝑥10−23 𝑥300
(6.625𝑥10−34 )2
= 5.657x1.807x1024 x2.892x10−6
𝑛𝑒 = 2.956x1019 /𝑚3
[Link] the Hall coefficient and electron mobility of germanium for a given sample( length=
1cm, breadth = 5mm, and thickness =1 mm).A current of 5 ma flows from a 1.35V supply
and develops a Hall voltage of 20 mV across the specimen in a magnetic field of 0.45Wb/𝑚2
Given: I=5mA=5x10−3 A,V=1.35V,L=1cm =1x 10−2m, w =5mm=5x10−3 𝑚,
d =1mm=1x10−3 𝑚, 𝑉𝐻 = 20𝑚𝑉 = 20𝑥10−3 𝑉, B= 0.45 𝑊𝑏/𝑚2, 𝑅𝐻 = ? , 𝑛 = ?
𝑅𝐴 𝑉
Using 𝜌 = , R = 𝐼 and A = w x d ,we get
𝐿
𝑉𝑤𝑡 1.35𝑥5𝑥10−3 𝑥1𝑥10−3
𝜌= = = 0.135 Ω-m.
𝐼𝐿 5𝑥10−3 𝑥1𝑥 10−2
1.18𝑉𝐻 𝑤 1.18𝑥20𝑥10−3 𝑥5𝑥10−3
𝑅𝐻 = = = 0.0524 𝑚3 /𝐶
𝐼𝐵 5𝑥10−3 𝑥0.45
𝑅𝐻 0.0524
Also, 𝜇 = = = 0.3882 𝑚2 /𝑉𝑠
𝜌 0.135
Dielectric polarizability(𝜶) is defined as the induced dipole moment of an atom per unit
𝝁 𝑷
electric field intensity. 𝜶 = 𝑬 = where N = 𝑵𝒖𝒎𝒃𝒆𝒓 𝒐𝒇 𝒅𝒊𝒑𝒐𝒍𝒆𝒔 𝒑𝒆𝒓 𝒖𝒏𝒊𝒕 𝒗𝒐𝒍𝒖𝒎𝒆.
𝑵𝑬
POLAR DIELECTRICS and NON-POLAR DIELECTRICS
Polar dielectrics are the dielectric material doesn’t possess any free electrons. All the
electrons are bound very strongly to the respective nuclei of the parent molecule. Each
molecule or atom in the normal state consists of equal amount of positively and negatively
charges. In polar dielectrics effective center of positively and negatively charges doesn’t
coincide. Ex: HCL, nitrobenzene, hence polar dielectrics has permanent dipole..
Non-Polar dielectrics are the dielectric materials in which effective center of positively and
negatively charges coincide., which results in zero dipole in the absence of an external
electric field. Ex: Paraffin, Symmetric molecules like (monoatomic)He, Ne, Ar, Xe etc and
𝐻2 , 𝑁2 , 𝐶𝑙2 etc
The application of an electric field tends to displace these charges ,creating dipoles(and
hence polarization)
Polarisation(P) : The process of producing electric dipoles, which are oriented along the
field direction is called Polarization in dielectrics. Or It is defined as the electric dipole
moment per unit volume.
𝑬𝒍𝒆𝒄𝒕𝒓𝒊𝒄 𝒅𝒊𝒑𝒐𝒍𝒆 𝒎𝒐𝒎𝒆𝒏𝒕 𝝁
P= = 𝑽 … C/𝒎𝟐
𝑽𝒐𝒍𝒖𝒎𝒆
𝜶𝑬
P= ∵ 𝝁 = 𝜶𝑬
𝑽
𝑷 = N 𝜶𝑬 where N = 𝑵𝒖𝒎𝒃𝒆𝒓 𝒐𝒇 𝒅𝒊𝒑𝒐𝒍𝒆𝒔 𝒑𝒆𝒓 𝒖𝒏𝒊𝒕 volume.
Relation between Polarization and dielectric constatnt is given by,
𝑷 = 𝜺𝒐 (𝜺𝒓 − 𝟏)𝑬
Types of Polarization:
There are mainly three types of dielectric polarization namely,
1) Electronic polarization 𝑃𝑒 = 𝑁𝛼𝑒 𝐸
2) Ionic polarization 𝑃𝑖 = 𝑁𝛼𝑖 𝐸
3) Orientation polarization 𝑃𝑜 = 𝑁𝛼𝑜 𝐸
1. Electronic polarization: It occurs due to displacement of the positive and negative charges in
a dielectric material owing to the application of an E.F, The separation created between the
charges leads to the development of a dipole [Link] process occurs throughout the
material. Thus the material as a whole will be polarized.
𝜺𝒐 (𝜺𝒓 − 𝟏)
𝛼𝑒 = where,
𝑁
+ - + +- +
- + - - + -
+ - + +- +
“ The internal field/Local field is the E.F that acts at the site of any given atom of a solid
dielectric subjected to an external E.F, and the resultant of the applied field and the field
due to all the surrounding dipoles”.
OR
“The total electric field at an atom site in a dielectric material due to applied external
electric field and induced various fields is called internal field”.
Consider a dielectric material kept in an applied E.F Ea, then internal field is given by
𝟏.𝟐 µ
Ei = Ea + where µ = α E
𝜫𝜺𝒐 𝒅𝟑
In 3-D case, (1/𝒅𝟑 ) could be replaced by N, the number of atoms per unit volume and
(1.2/ 𝜫) by a constant γ which depends on the crystal structure.
𝜸𝑵µ 𝜸
Hence, Ei = Ea + = Ea +[ ] P since Nµ = P
𝜺𝒐 𝜺𝒐
Where 𝜸 is the proportionality constant which is known as the internal field constant.
Expression for internal field by Lorentz method / Lorentz field:
In the 3-D case , if it is a cubic lattice, then it can be shown that γ = 1/3 in which event, the
internal field is named Lorentz field given by,
𝑷
𝑬𝑳𝒐𝒓𝒆𝒏𝒕𝒛 = 𝑬 +
𝟑𝜺𝟎
This equation is known as Lorentz relation
INTERNAL FIELD(LOCAL FIELD)/LORENTZ FIELD IN SOLIDS
Internal(Local) field is the resultant field experienced by a molecule/an atom in a solid due to
the external field and the fields produced by dipoles.
Internal field is the sum of the applied field and the induced field.
CLAUSIUS-MOSOTTI EQUATION:
Consider an elemental solid dielectric which exhibits only electronic polarizability. Solids such as
diamond , silicon and germanium crystals are made up of single type of atoms.
If 𝛼𝑒 is the electronic polarizability per atom,
𝑃
∴ 𝛼𝑒 = 𝑁 𝐸 where N – no of atoms per m3
𝑖
𝜸 𝑃
WKT, Ei = E +[𝜺 ] P , 𝛼𝑒 = 𝜸
𝒐 𝑁[𝑬 +[
𝜺𝒐 ] 𝑷]
𝑷
And also wkt, E = 𝜺 (𝜺 −𝟏) and also , If the internal field is assumed to be Lorentz field, 𝜸 =
𝒐 𝒓
𝑷
𝟏/𝟑. ∴ 𝜶𝒆 = 𝑷 𝑷
𝑵 [( (𝜺 + )]
𝜺𝒐 𝒓 −𝟏) 𝟑𝜺𝒐
𝑷
N𝜶𝒆 = 𝑷 𝟏 𝟏
[ + ]
𝜺𝒐 (𝜺𝒓 −𝟏) 𝟑
𝜺𝒐
N𝜶𝒆 = 𝟏 𝟏
+
(𝜺𝒓 −𝟏) 𝟑
𝑵𝜶𝒆 𝟏 𝟏
= 𝟏 𝟏 = 𝜺𝒓 + 𝟐
𝜺𝒐 +
(𝜺𝒓 −𝟏) 𝟑 𝟑(𝜺𝒓 −𝟏)
𝟑(𝜺𝒓 −𝟏) 𝑵𝜶𝒆
=
𝜺𝒓 + 𝟐 𝜺𝒐
DIELECTRIC MATERIALS:
1. Dielectric materials are mainly used as Insulating materials and to store electrical
charges in capacitors.
2. The dielectrics in general must have high resistivity, high/low dielectric constant,
low dielectric loss, adequate chemical stability, high moisture resistance and
suitable mechanical properties.
Dielectrics may be solids, liquids or gasses .
Solid dielectrics:
1. Solid dielectrics are used as dielectric materials in capacitors for storing electrical
charges. Ex:Polymers, ceramics, mica, barium titanate etc
2. Quartz crystal is used in ultrasonic transducer, crystal oscillator, filters etc
3. Lead zirconate titanate is used in the –preparation of microphone, spark generator,
ear phones etc
Liquid dielectrics(LDs):
1. Liquid dielectrics are used as a cooling medium in transformers and some electronic
equipments.
2. Liquid dielectrics are used as filling medium in capacitors, bushings etc
3. LDs are used as an insulating and arc-quenching medium in switchgear.
4. LDs impregnated with solid materials like paper etc are used in transformers,
switch gears, capacitors and cables.
Gaseous dielectrics:
1. Compressed air is used as a dielectric insulation in air blast circuit breaker.
2. Air is used as arc-extinguishing medium.
Application of dielectrics in Transformers
1. Transformer oil is special mineral oil with high dielectric strength used for
insulation and cooling of transformer.
2. It transfer heat by convection from windings and core to cooling surface.
3. It also maintains the insulation of the windings.
Sludge formation takes place in the oil due to moisture, dirt or some foreign matter in the
oil which is harmful. Sludge formation reduce the rate of heat transfer ,Ducts are clogged
and operating temperature increases. The oil must undergo dehydration periodically and
tested at regular intervals.
PROBLEMS ON DIELECTRICS
1. If NaCl crystal is subjected to an electric field of 1000 V/m and the resulting
polarization is 4.3 x 𝟏𝟎−𝟖 C/𝒎𝟐 , calculate the dielectric constant of NaCl.
Ans: Given E = 1000 V/m , P = 4.3 x 𝟏𝟎−𝟖 C/𝒎𝟐 , 𝜺𝟎 = 𝟖. 𝟖𝟓𝟒 x 𝟏𝟎−𝟏𝟐 F/𝒎𝟐 , 𝜺𝒓 = ?
Using P = 𝜺𝟎 (𝜺𝒓 − 𝟏)𝑬 , we get
𝑷
𝜺𝒓 = 1+ 𝜺𝟎 𝑬
𝟒.𝟑 𝒙 𝟏𝟎−𝟖
= 𝟏 + 𝟖.𝟖𝟓𝟒 𝒙 𝟏𝟎−𝟏𝟐 𝒙𝟏𝟎𝟎𝟎
= 𝟏 + 4.857
= 𝟓. 𝟕𝟓𝟕
2. What is the polarization produced in sodium chloride by an electric Field of 600
V/mm if it has a dielectric constant of 6 ?
Ans: Given E = 𝟔𝟎𝟎 𝑽/𝒎𝒎 = 600 x 𝟏𝟎𝟑 V/m , 𝜺𝒓 = 𝟔 , 𝜺𝟎 = 𝟖. 𝟖𝟓𝟒 x 𝟏𝟎−𝟏𝟐 F/𝒎𝟐 , 𝑷 = ?
Using P = 𝜺𝟎 (𝜺𝒓 − 𝟏)𝑬
= 𝟖. 𝟖𝟓𝟒 𝒙 𝟏𝟎−𝟏𝟐 (𝟔 − 𝟏)𝟔𝟎𝟎 x 𝟏𝟎𝟑
= 2.656 x 𝟏𝟎−𝟓 C/𝒎𝟐
3. The dielectric constant of sulphur is 3.4. assuming a cubic lattice for its structure,
calculate the electronic polarizability of sulphur. Given sulpher density =
𝟐. 𝟎𝟕𝒈𝒎/𝒄𝒄,Atomic weight = 𝟑𝟐. 𝟎𝟕
Ans: Given D = 𝟐. 𝟎𝟕𝒈𝒎/𝒄𝒄 = 𝟐. 𝟎𝟕 x 𝟏𝟎𝟑 kg/𝒎𝟑 , 𝜺𝒓 = 𝟑. 𝟒 , 𝑴 = 𝟑𝟐. 𝟎𝟕, 𝜶𝒆 = ?
𝑵𝑨 = 𝟔. 𝟎𝟐𝟓 𝒙 𝟏𝟎𝟐𝟔 atoms/K mole, 𝜺𝟎 = 𝟖. 𝟖𝟓𝟒 x 𝟏𝟎−𝟏𝟐 F/𝒎𝟐
𝑵𝑨 𝑫 𝟔.𝟎𝟐𝟓 𝒙 𝟏𝟎𝟐𝟔 𝒙 𝟐.𝟎𝟕 𝒙 𝟏𝟎𝟑
Number of atoms per unit volume, N = =
𝑴 𝟑𝟐.𝟎𝟕
= 3.889 x 𝟏𝟎 atoms/𝒎𝟑 𝟐𝟖
(𝟏 + 𝟐𝒙𝟎. 𝟕𝟗𝟎𝟔)
= = 𝟏𝟐. 𝟑𝟐𝟕 = 𝟏𝟐. 𝟑𝟑
(𝟏 − 𝟎. 𝟕𝟗𝟎𝟔)
6. The dielectric constant of He gas at NTP is 1.0000684. Calculate the electronic
polarizability of He atoms if the gas contains 2.7 x 𝟏𝟎𝟐𝟓 atoms/𝒎𝟑 and hence
evaluate the radius of He atoms.
𝑭
Ans: Given, 𝜺𝟎 = 𝟖. 𝟖𝟓𝟒 𝒙 𝟏𝟎−𝟏𝟐 𝒎𝟐 , 𝑵 = 𝟐. 𝟕 𝒙 𝟏𝟎𝟐𝟓 𝒂𝒕𝒐𝒎𝒔/𝒎𝟑 , 𝜺𝒓 = 𝟏. 𝟎𝟎𝟎𝟎𝟔𝟖𝟒, 𝜶𝒆 = ?
& R =?
𝜺𝟎 (𝜺𝒓 −𝟏) 𝟖.𝟖𝟓𝟒 𝒙 𝟏𝟎−𝟏𝟐 (𝟏.𝟎𝟎𝟎𝟎𝟔𝟖𝟒−𝟏)
Using , 𝜶𝒆 = = = 2.243 x 𝟏𝟎−𝟒𝟏 F𝒎𝟐
𝑵 𝟐.𝟕 𝒙 𝟏𝟎𝟐𝟓
𝟏/𝟑 𝟏/𝟑
𝜶 𝟐.𝟐𝟒𝟑 𝒙 𝟏𝟎−𝟒𝟏
Also Radius ,R = (𝟒𝝅𝜺𝒆 ) = (𝟒𝝅𝒙𝟖.𝟖𝟓𝟒 𝒙 𝟏𝟎−𝟏𝟐 ) = 𝟓. 𝟖𝟔𝟒 𝒙 𝟏𝟎−𝟏𝟏 𝒎
𝟎
*****