Mod 3
Mod 3
8πυ 2 dυ
G (ν ) dν = C3
The total energy U (ν ) dν per unit volume in the cavity in the frequency interval
from ν to ν+d ν is therefore
U (ν ) dν = ε G (ν ) dν
8πkT 2
U (ν ) dν = 3
υ dν
c
It contains everything that classical physics can say about the spectrum of black body
Radiation
Energy density is proportional to υ 2
; at high frequencies U (ν )dν ∞
Molecules can only have discrete values of energy En, given by:
En = nhν
where n is a positive integer called a quantum number and ν is the natural
frequency of oscillation of the molecules.
Because the energy of a molecule can only have discrete values, we say
the energy is quantized. Each discrete energy level represents a specific
quantum state.
The molecules emit or absorb energy in discrete packets that later became
known as photons. The molecules emit or absorb photons by 'jumping' from
one quantum state to another.
If the jump is downward from state to an adjacent lower state, the amount
of energy radiated by the molecule in a single photon is hν. A molecule emits
or absorbs energy only when it changes quantum states.
The RayleighJeans curve agrees with the Planck radiation formula for longer
wavelengths, (low frequencies)
Planck’s constant h = 6.626×10-34 J s
Average energy of an oscillator whose
frequency of vibration is υ.
hυ
E= hυ / kT
(e − 1)
Energy radiated per unit volume in the
frequency interval υ and υ+dυ
8πhν 3 dv
U (v)dv =
c 3 e hv / k BT − 1
This is called Planck’s radiation formula.
h –Planck’s constant
c –velocity of light
kB – Boltzmann constant 1.38 x 10-23 J/K
T- Absolute temperature
At high frequencies hυ >> kT and e hυ kT ∞
At low frequencies
hυ
<< 1
kT
2
x
e x = 1 + x + + ....
2!
If x is small ex = 1+ x
1 1 kT
= =
e hυ kT − 1 1 + hυ − 1 hυ
kT
At low frequencies Planck’s formula becomes
8πhν 3 kT
U (v)dv = dv ( )
c 3
hυ
8πkTν 2
= 3
dv
c
which is Rayleigh Jeans formula.
Engineering Physics
PHY 1001
Lecture-2
M. Ummal Momeen
School of Advanced Sciences,
VIT University, Vellore Campus.
Course plan for Lecture-2
Compton effect
Derivation of Compton shift and its
IMPLICATIONS; Comparison of experimental
and theoretical prediction.
The Compton Effect is one of the most important experiments
according to quantum mechanics.
∆x∆px ≥ /2
∆E ∆t ≥ /2
Example of Baseball
A pitcher throws a 0.1-kg baseball at 40 m/s
y = A cos (ω t − kx ) 1
y = A cos (ω t − kx ) − i A sin (ω t − kx ) 2
y = Ae − i (ωt - kx )
Only real part of (2) has significance in the case of waves in a stretched string.
‘y’ means displacement , imaginary is discarded as irrelevant.
ψ = Ae −i (ωt - kx )
It convenient to change ω and k in terms of total energy ‘E’ and momentum
‘p’ of the particle being described by ‘ψ’
−
i
( Et − px )
ψ = Ae -3
Since
E= hυ = 2π υ* h/ 2π = ħ ω
∴E= ħ ω ω=E/ ħ
λ =h/p p =h/ λ = = (h/ 2π)* (2π / λ)
∴ P= ħk k = P/ ħ
(3) describes the wave equivalent of an unrestricted particles
of total energy ‘E’ and momentum ‘p’ moving in + x direction
Wave function ‘ψ’ given by (3) is correct only for free moving
particle
However motion of particle with various restriction are
interested
e.g. Electron bound to an atom by electric filed of nucleus
A particle can have as a wave only under motion,
So the total energy E of the particle is sum of K.E and its potential energy U,
Where U is in a function of position ‘x’ and time ‘t’
1 2
E = mv + U ( x, t )
2
2 2
1mv
E= +U
2 m
p2
E= +U -(4)
2m
multiplying both side of eq. 4 with wave function ψ
p2
Eψ = ψ + Uψ -(5)
2m
Aim to obtain the fundamental differential equation for ‘ψ’
∂ψ 2 ∂ 2ψ -(8)
i =− + Uψ
∂t 2m ∂x 2
in three dimensions the time - dependent form of schrodinger eq.
∂ψ 2 ∂ 2ψ ∂ 2ψ ∂ 2ψ
i =− 2 + 2 + 2 + Uψ
∂t 2m ∂x ∂y ∂z
∂ψ 2 2
i = − ∇ + U ψ
∂t 2m -(9)
Eψ = Hψ
∂
E → i → energy operator
∂t
2 2
H → − ∇ + U → Hamiltonian operator
2m
P → −i∇ → Momentum operator
Schrodinger’s time independent equation (steady state equation)
Let us consider a system of stationary wave associated a moving particle.
Let ψ be the wave function of particle along x.
iE
− t
Ψ = ψe ----- 5
∂Ψ 2 ∂ 2Ψ ----- 6
i =− + UΨ
∂t 2m ∂x 2
Schrodinger’s time independent equation
−i −i
∂Ψ ip
i
px ip
Et Et
= Ae e
= ψe
∂x
−i −i
∂ Ψ i p
2 2 2 i 2
px Et p Et
= 2 Ae e
= − 2 ψe
∂x 2
−i
2 ∂ Ψ
2
Et
p ψe
2
= − -----------(7)
∂x 2
Schrodinger’s time independent equation
−i
∂Ψ ∂ψ Et
= e
∂x ∂x
−i
∂ Ψ ∂ ψ Et
2 2
= 2 e
∂x 2
∂x
-----------(8)
Schrodinger’s time independent equation
Differentiating eq. 3 w.r.t. t
−i
∂Ψ − iE Et
ip
x
=
Ae e
∂t
−i -----------(9)
− iE Et
= ψe
Substitute equations 5, 8 and 9 in equation 6
−i
− iE Et − 2 ∂ 2ψ − t
iE iE
− t
i ( ψe ) = 2 e + Uψe
2m ∂x
− 2 ∂ 2ψ
Eψ = 2 + Uψ
2m ∂x
2 ∂ 2ψ
2 + ( E − U )ψ = 0
2m ∂x
∂ 2ψ 2m
+ 2 ( E − U )ψ = 0
∂x 2
if in 3 dimension
∂ 2ψ ∂ 2ψ ∂ 2ψ
= − 2 (E − U )ψ
2m
+ +
∂x 2
∂y 2
∂z 2
∇ ψ = − 2 (E − U )ψ
2 2m
∇ − laplacian operator
therefore
∇ ψ + 2 (E − U )ψ = 0
2 2m
∂ ∂ ∂
∇ = iˆ + j +k
∂x ∂y ∂z
Schrodinger equation obtained here is for wave function of
a freely moving particle
Let us consider
- motion of a particle
along x – direction
within the region x= 0 and x= L
rigid walls of infinite height
- particle does not loss energy when it collides on walls
Particle cannot have infinite energy so, it can not exist outside the
box.
x=0 x=L
+ 2 Eψ = 0
∂x2
d 2ψ
2
+ k 2
ψ =0 Total derivative is the same as partial
Derivative becs, ψ is the function only
dx
Of x
2m
where k = 2 E 2
ψ ( x) = A sin kx + B cos kx
A and B are constants to be determined from boundary conditions
At x = 0, ψ=0
kL = nπ ; where n = 1,2,3…..
k = nπ / L
√(2mE/ ħ2 ) = nπ / L
2m n 2π 2
En = 2
2
L
n 2π 2 2
En = 2
where n = 1,2,3.... ; are energy eigen values
2mL
2mEn
ψ ( x) = A sin x
nπ
ψ ( x) = A sin x
L
∫ ψ ( x) dx = 1
2
−∞
L
∫ ψ ( x) dx = 1
2
nπ
L
A ∫ sin
2
x dx = 1
2
0 L
A nπ
2 L L
2 2nπ L 0 2
2
A
[L] = 1 →→→ A = 2
2 L
The normalized wave function of the particle
2 nπ
ψn = sin x n = 1,2,3....
L L
0.4 0.4
0.2
|ψ4|2 0.0
0.2
0.0 ψ4
-0.2 -0.2
-0.4 -0.4
0.4 0.4
0.2 0.2
0.0
-0.2 ψ3 |ψ3| -0.2
2 0.0
-0.4 -0.4
0.4 0.4
0.2 0.2
|ψ2|2 -0.2
0.0
-0.2 ψ2 0.0
-0.4 -0.4
0.4 0.4
0.2 0.2
0.0 ψ1 |ψ1| 0.0
2
-0.2 -0.2
-0.4 -0.4
0 2 4 6 8 10 0 2 4 6 8 10
A A
At particular place in the box the probability of the
particle being present may
Vary for different quantum number
x2
Px1, x 2 = ∫ ψ ( x) dx
2
x1
2 nπ
x2
2
= ∫ sin x dx
L x1 L
x2
x 1 2nπ
= − sin x
L 2nπ L x1
n= 1 P x1,x2 =0.198 then 19.8 percent
n= 2 P x1,x2 =0.0065 then 0.65 percent
PARTICLE IN A 3-D BOX
Question: An electron is in 1D box of 1nm
length. What is the probability of locating the
electron between x=0 and x=0.2nm in its lowest
energy state?
QUESTION: AN ELECTRON IS IN 1D BOX OF 1NM LENGTH. WHAT IS
THE PROBABILITY OF LOCATING THE ELECTRON BETWEEN X=0 AND
X=0.2NM IN ITS LOWEST ENERGY STATE?
Solution:
QUESTION: WHAT ARE THE MOST
LIKELY LOCATIONS OF A PARTICLE IN A
BOX OF LENGTH L IN THE STATE N=3
Example: What are the most likely locations of a particle in a
box of length L in the state n=3
NORMALIZATION AND PROBABILITY
The probability P(x) dx of a particle being between x
and X + dx was given in the equation
39
The Wavefunction
E = hν
p=h/λ
h
λ=
mv
9
h h
de Broglie wavelength λ = =
p mv
h is Planck' s Constant
m is the mass of the particle
v is the velocity of the particle
for an electron with Kinetic Energy ' E '
accelerated by a Potential difference 'V '
h h
Then λ = =
2mE 2meV
substituting for h , m , and e we get
6.625 ×10 −34 1.226
λ = = nm
2 × 9.11× 10 −31 × 1.602 × 10 −19 ×V V
thus for V = 100 Volts
1.226
λ = = 0.1226 nm
100
The frequency
E= hυ
In other words,
υ=E/h
Example: de Broglie wavelength of an electron
Mass = 1 kg
Speed = 1 m / sec
X-rays electrons
Evidence:
– electron diffraction
– electron interference (double-slit experiment)
Applications:
– Bragg scattering
– Electron microscopes
– Electron- and proton-beam lithography
Wave-Particle Duality
c2
vp =
v
Where c = velocity of light and v = is velocity of the particle.
The above equation gives the relationship between the phase velocity and
particle velocity.
It is clear from the above equation that, Phase velocity is not only greater
than the velocity of the particle but also greater than the velocity of light,
which can never happen. Therefore phase velocity has no physical
meaning in case of matter waves. Thus a concept of group velocity was
23
introduced.
Matter Waves
GROUP VELOCITY
Since phase velocity has no meaning, the concept of group velocity was
introduced as follows.
“ Matter wave is regarded as the resultant of the superposition of large
number of component waves all traveling with different velocities. The resultant
is in the form of a packet called wave packet or wave group. The velocity with
which this wave group travels is called group velocity.” The group velocity is
represented by vg.
V
g
Particle
Vp
24
DeBroglie Hypothesis
DeBroglie = h/mv = h/p
In this case, we are considering the
electron to be a WAVE, and
the electron wave will “fit” around the orbit
if the momentum (and energy) is just right
(as in the above relation). But this will happen
only for specific cases - and those are the
specific allowed orbits (rn) and energies (En)
that are allowed in the Bohr Theory!
What we now have is a wave/particle duality for light
(E&M vs photon), AND a wave/particle duality for
electrons!
DeBroglie Hypothesis
If the electron behaves as a wave, with
= h/mv, then we should be able to test this
wave behavior via interference and
diffraction.
In fact, experiments show that electrons DO
EXHIBIT INTERFERENCE when they go
through multiple slits, just as the DeBroglie
Hypothesis indicates.
Properties of matter waves
•The lighter the particle, greater the wavelength associated with it
•Smaller the velocity of the particle greater the wavelength associated
with it
•When v=0, λ= infinity, this shows that matter waves are generated by
the motion of particles. These waves are produced whether the particles
are charged or uncharged. Wavelength is independent of charge. This
fact reveals that these waves are not electromagnetic and they are new
kind of waves
•The velocity of matter waves is not constant while velocity of
electromagnetic wave is constant
•Velocity of matter wave is greater than velocity of light
Proof:
A particle in motion with an associated wave has two different velocities
• Due to the mechanical motion of the particle v and
the other related to the propagation of the wave denoted by ω
We know that E=hν 2
mc
E=mc2 , ν=
h
e e det. e e
e
e scatter off atoms
e e
e e e
e
move detector around,
see what angle electrons coming off
Ni
• If electrons are “just” particles, we expect a smooth
monotonic dependence of scattered intensity on angle and
voltage because only elastic collisions are involved
• Diffraction pattern similar to X-rays would be observed if
electrons behave as waves
Davisson and Germer Experiment
Davisson and Germer Experiment
• Observations:
– Intensity was stronger for
certain angles for specific
accelerating voltages (i.e.
for specific electron
energies)
– Electrons were reflected in
almost the same way that
X-rays of comparable
wavelength
Davisson and Germer Experiment
• Observations:
– Current vs accelerating
voltage has a maximum,
i.e. the highest number of
electrons is scattered in a
specific direction
– This can’t be explained by
particle-like nature of
electrons electrons
scattered on crystals
behave as waves
p2 h
E , p 2mE , B
2m 2mE
6.63 10 34 J - sec
B 1.67 A
31 18
2 9.110 kg 8.6 10 J
2d sin
o o
d111 0.91 A; X -ray 1.65 A
65 50