Applied Physics Unit-1 Notes
Applied Physics Unit-1 Notes
Tech CSE(AIML)/CSE(DS)/CSE/ECE/EEE/CSBS/ME/CE
Max Planck in 1900 introduced the quantum theory of radiation to explain the distribution of
energy in the spectrum of black body radiation i.e. frequency distribution of thermal radiation.
Planck assumptions are
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1. The atomic oscillators in a body cannot have any arbitrary amount of energy but can have
only discrete units of energy given by E = nhν, where n = 0, 1, 2…… (Any positive integer),
h = Planck’s constant and ν = frequency of the oscillator.
2. The oscillator can emit or absorb energy only in the form of wave packets of energy(hν) in
indivisible discrete units. The emission or absorption of energy occurs only when the
oscillator jumps from one energy state to another along with the energy difference given
by E2-E1= (n2-n1)hν.
The energy of each quantum is a minimum amount of energy that cannot be further sub divided.
The radiation of energy emitted or absorbed in a discontinuous manner and in the form of
quantum is called the Planck’s quantum hypothesis.
The emission of electrons from a metal plate when illuminated by light radiation of
suitable wave length or frequency is called photoelectric effect. The emitted electrons
are called photo electrons. This effect was discovered by Hertz, when ultraviolet light
falls on zinc plate.
Alkali metals like Li, Na, K etc. eject electrons when visible light falls on them.
Millikan investigated this effect with a number of alkali metals over a wide range of
light frequencies and was awarded Noble prize in 1923.
Figure 1
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(i) Apart of its energy is used to free the electron from the atom and away from the metal
surface. This energy is known as photoelectric work function of the metal. This is
denoted by W0.
(ii) The other part is used in giving kinetic energy ( 𝑚𝑣 ) to the electron.
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Threshold frequency is defined as the minimum frequency which can cause photoelectric
emission.
If the frequency of the photon is below threshold frequency no emission of electrons will take
place. Corresponding to threshold frequency, we define long wavelength limit (λ 0). It
represents the upper limit of wavelength for photoelectric effect. Its physical significance is
that radiations having wavelength longer than λ0 would not be able to eject electrons from a
given metal surface whereas those having λ< λ0, will. The value of λ0 is given by
c = ν0λ0
λ0 = =
× × ⋅ ×
λ0 =
. ×
= metre.
. ×
λ0 =
. ×
= A0 ---------------- (3)
hν = hν0 + 𝑚𝑣
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𝑚𝑣 = hν - W0
K.E. = 𝑚𝑣 ∝ hν
𝑣 ∝ν
𝑚𝑣 = hν - hν0
eV0 = hν - hν0
V0 = − 𝜗 ------------(7)
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There is no time lag between incident radiation (photon) and ejected photoelectron.
The rate of photo-emission is directly proportional to intensity of incident radiation
(light).
The velocity and hence the kinetic energy of photo-electrons is independent of intensity
of incident light.
The velocity and hence the kinetic energy of photo-electrons is directly proportional to
frequency of incident radiation.
The emission of electron take place above a certain frequency known as threshold
frequency. This frequency is characteristic frequency of photo-metal used.
An electromagnetic wave behaves like particles, particles like electrons behave like waves called
matter waves, also called de-Broglie matter waves. The wave length of matter waves is derived on
the analogy of radiation.
Based on Planck’s theory of radiation, the energy of a photon is given by
E = hν = ….. (1)
λ
De-Broglie proposed the concept of matter waves, according to which a material particle of mass
’m’, moving with a velocity ’v’ should have an associated wavelength ‘𝜆′ called de-Broglie
wavelength.
𝐡 𝐡
𝛌= = … (4) is called de-Broglie’s wave equation.
𝐦𝐯 𝐩
Wavelength is associated with moving particle and independent of charge of the particles.
Greater the mass and velocity of the particle, lesser will be the wavelength.
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2𝑒𝑉
𝑣=
𝑚
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From fig, the electron beam from electron gun which consists of a tungsten filament ‘F’ heated by
a low-tension battery ‘B1’ are accelerated to a desired velocity by applying suitable potential from
a high-tension battery ‘B2’.
The accelerated electrons are collimated into a fine beam by allowing them to pass thorough a
system of pinholes in the cylinder ‘A’.
The fast-moving electron beam is made to strike the target (nickel crystal) capable of rotating about
an axis perpendicular to the plane of diagram.
The electrons are scattered in all directions by atomic planes of a crystal and intensity of scattered
electron beam in all directions can be measured by the electron collector and can be rotated about
the same axis as the target.
The collector is connected to a sensitive galvanometer whose deflection is proportional to the
intensity of electron beam entering the collector.
When electron beam accelerated by 54 V was directed to strike the given nickel crystal, a sharp
maximum in the electron diffraction occurred at an angle of 50 0 with the incident beam.
The incident beam and the diffracted beam make an angle of 65 0 with the family of Bragg’s planes.
The whole instrument is kept in an evacuated chamber.
The spacing of planes in Nickel crystal as determined by x-ray diffraction is 0.091nm
From Bragg’s law 2dsinθ = n λ i.e 2 × 0.091 × 10 × 𝑠𝑖𝑛65° = 1 × λ
λ = 0.1648 nm
Therefore, for a 54 V electron beam, the de-Broglie wavelength associated with the electron is
.
given by λ= A° = 0.1668 nm
√
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This wavelength agrees well with the experimental value. Thus, Davison and Germer experiment
provides a direct verification of de-Broglie hypothesis of wave nature of moving particles.
6). HEISENBERG’S UNCERTAINTY PRINCIPLE:
Heisenberg a German scientist in 1927 gave uncertainty principle which states that “The
determination of exact position and momentum of a moving particle simultaneously is
impossible’’.
In general, if △x represents the uncertainty in measurement of position of particle along x-axis,
and △p represents uncertainty in measurement of momentum, then
△𝒙 . △p = h or
limitation to find the position and momentum of a particle is (△ x). (△ p) ≥ i.e. Heisenberg
π
uncertainty principle states that both the position and momentum cannot be measured
simultaneously with perfect accuracy.
According to Classical mechanics, a moving particle at any instant has fixed position in space and
definite momentum which can be determined simultaneously with any desired accuracy. This
assumption is true for objects of appreciable size, but fails in particles of atomic dimensions.
Since a moving atomic particle has to be regarded as a de-Broglie wave group, there is a limit to
measure particle properties.
According to Born probability interpretation, the particle may be found anywhere within the wave
group moving with group velocity.
If the group is considered to be narrow, it is easier to locate its position, but the uncertainty in
calculating its velocity and momentum increases.
If the group is wide, its momentum is estimated easily, but there is great uncertainty about the
exact location of the particle.
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The wave function 𝛙 is unable to give all possible information about the particle. 𝛙is a complex
quantity and has no direct physical meaning. It is only a mathematical tool in order to represent
the variable physical quantities in quantum mechanics.
Born suggested that, the value of wave function associated with a moving particle at the position
co-ordinates (x,y,z) in space, and at the time instant ‘t’ is related in finding the particle at certain
location and certain period of time ‘t’.
If 𝛙 represents the probability of finding the particle, then it can have two cases.
Case 1: certainty of its Presence: +ve probability
Case 2: certainty of its absence: - ve probability, but –ve probability is meaningless,
Hence the wave function 𝛙 is complex number and is of the form a+ib
Even though 𝛙 has no physical meaning, the square of its absolute magnitude |𝛙 | gives a definite
meaning and is obtained by multiplying the complex number with its complex conjugate then
|𝛙 |represents the probability density ‘p’ of locating the particle at a place at a given instant of
time. And has real and positive solutions.
𝛙(𝐱, 𝐲, 𝐳, 𝐭) = 𝐚 + 𝐢𝐛
𝛙∗ (𝐱, 𝐲, 𝐳, 𝐭) = 𝐚 − 𝐢𝐛
𝐩 = 𝛙𝛙∗ = |𝛙 | = 𝑎 + 𝑏
Where ‘P’ is called the probability density of the wave function.
If the particle is moving in a volume ‘V’, then the probability of finding the particle in a volume
element dv, surrounding the point x, y, z and at instant ‘t’ is Pdv
∞
𝛙𝟐 𝒅𝒗 = 𝟏 𝑖𝑓 𝑝𝑎𝑟𝑡𝑖𝑐𝑙𝑒 𝑖𝑠 𝑝𝑟𝑒𝑠𝑒𝑛𝑡
∞
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𝛙 can be considered as probability amplitude since it is used to find the location of the
particle.
Schrodinger describes the wave nature of a particle in mathematical form and is known as
Schrodinger’s wave equation.
Consider a plane wave moving along +ve x- direction with velocity ‘v’. The equation of the wave
= −𝑎 sin (𝑥 − 𝑣𝑡)….(2)
λ λ
+ 𝑦 = 0…… (3)
λ
𝑑 ψ 2𝜋
+ ψ=0
𝑑𝑥 λ
ψ
+ ψ = 0…… (4)
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𝑑 ψ 4𝜋 2𝑚(𝐸 − 𝑉)
+ ψ=0
𝑑𝑥 ℎ
𝒅𝟐 𝛙 𝟖𝝅𝟐 𝒎(𝑬 𝑽)
+ 𝛙 = 𝟎…... (8)
𝒅𝒙𝟐 𝒉𝟐
This equation is known as Schrodinger’s time independent wave equation in ONE dimension.
In THREE dimensions, it can be written as
( )
∇ ψ+ ψ = 0…… (9)
𝟐𝒎(𝑬 − 𝑽)
𝛁𝟐𝛙 + 𝛙=𝟎
ℏ𝟐
For a free particle, the P.E is equal to zero i.e. V=0 in equation (9)
Therefore, the Schrodinger’s time independent wave equation for a free particle is
𝟖𝝅𝟐 𝒎𝑬
𝛁𝟐𝛙 + 𝛙=𝟎
𝒉𝟐
Assume that the particle is freely moving inside the box. The motion of the particle is restricted
by the walls of the box. The particle is bouncing back and forth between the walls of the box at x
= 0 and x = L. For a freely moving particle within the potential box, the potential energy is zero,
but abruptly to infinity at x = 0 and x =L as shown in fig.
0, 0<𝑥<𝐿
i.e., 𝑉(𝑥) =
∞, 𝑥 ≥ 0 𝑜𝑟 𝑥 ≤ 0
The Schrödinger one – dimensional time independent eqn. is
( )
+ ψ = 0 ------ (1)
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( )
Taking =𝑘 ---------- (3)
= 1, 2, 3, …. ( n ≠ 0 )
n = 2, 𝐸 = or 𝐸 = 4 𝐸
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Therefore, the particle in the box can have discrete values of energies. These values are quantized.
The values corresponding to each 𝐸 value is known as Eigen energy values.
Substituting the eqn. (6) and eqn. (8) in eqn. (5), we get,
𝒏𝝅𝒙
𝝍(𝒙) = 𝑨 𝒔𝒊𝒏 ----------- (9)
𝑳
In order to find the value of A, then we must normalize the wave function. We recognize that the
particle is definitely present inside the box. |ψ|2 is the probability of finding the particle at a
particular point in space, so the integral of this value over all x must be equal to 1:
𝑳
∫𝟎 |𝛙(𝒙)|𝟐 𝒅𝒙 = 𝟏 ------- (10)
Substituting eqn. (9) in eqn. (10), we get,
𝑳 𝒏𝝅𝒙 𝑳𝟏 𝟐𝒏𝝅𝒙
∫𝟎 𝑨𝟐 𝒔𝒊𝒏𝟐 𝑳
𝒅𝒙 = 𝟏 ⟹ 𝑨𝟐 ∫𝟎
𝟐
𝟏 − 𝒄𝒐𝒔
𝑳
𝒅𝒙 = 𝟏
𝟐𝒏𝝅𝒙 𝑳
𝑨𝟐 𝒔𝒊𝒏 𝑨𝟐
or 𝒙− 𝟐𝒏𝝅
𝑳
=𝟏 ⟹ [(𝑳 − 𝟎) − (𝟎 − 𝟎)] = 𝟏
𝟐 𝟐
𝑳 𝟎
𝑨𝟐 𝑳 𝟐
or =𝟏 ⇒𝑨= --------- (11)
𝟐 𝑳
Eqn.(12) represents the probability amplitude of the particle in n th level of the given potential
region.
The wave function is given by eqn. (12).
The normalized wave functions Ψ1, Ψ2, Ψ3
given by eqn. (12) is plotted. The values
corresponding to each En value is known as
Eigen value and the corresponding wave
function is known as Eigen function.
The wave function Ψ1, has two nodes at
x = 0 & x = L.
The wave function Ψ2, has three nodes at
x = 0, x = L/2 & x = L.
The wave function Ψ3, has four nodes at x = 0, x = L/3, x = 2L/3 & at x = L.
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SOLIDS
Origin of energy bands in solids:
Solids are usually moderately strong, slightly elastic structures. The individual atoms are
held together in solids by inter-atomic forces or bonds. In addition to these attractive forces,
repulsive forces also act and hence solids are not easily compressed. The attractive forces between
the atoms are basically electrostatic in origin. The bonding is strongly dependent on the electronic
structure of the atoms. The attraction between the atoms brings them closer until the individual
electron clouds begin to overlap. A strong
repulsive force arises to comply with Pauli’s
exclusion principle. When the attractive force
and the repulsive force between any two
atoms occupy a stable position with a
minimum potential energy. The spacing
between the atoms under this condition is
called equilibrium spacing.
In an isolated atom, the electrons are
tightly bound and have discrete, sharp energy
levels. When two identical atoms are brought
closer, the outermost orbits of these atoms overlap and interact. When the wave functions of the
electrons on different atoms begin to overlap considerably, the energy levels corresponding to
those wave functions split. if more atoms are brought together more levels are formed and for a
solid of N atoms, each of the energy levels of an atom splits into N levels of energy. The levels are
so close together that they form an almost continuous band. The width of this band depends on the
degree of overlap of electrons of adjacent atoms and is largest for the outermost atomic electrons.
In solid many atoms are brought together so that the split energy levels form a set of bands of very
closely spaced levels with forbidden energy gaps between them.
CLASSIFICATION OF MATERIALS :
The electrons first occupy the lower energy bands and are of no importance in determining
many of the electrical properties of solids. Instead, the electrons in the higher energy bands of
solids are important in determining many of the physical properties of solids. Hence the two
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allowed energy bands called valence and conduction bands are required. The gap between these
two allowed bands is called forbidden energy gap or band gap since electrons can’t have any
energy values in the forbidden energy gap. The valence band is occupied by valence electrons
since they are responsible for electrical, thermal and optical properties of solids. Above the valence
band we have the conduction band which is vacant at 0 K. According to the gap between the bands
and band occupation by electrons, all solids can be classified broadly into two groups.
In the first group of solids called metals
there is a partially filled band immediately
above the uppermost filled band. This is
possible when the valence band is partially
filled or a completely filled valence band
overlaps with the partially filled conduction
band.
In the second group of solids, there is a
gap called band gap between the completely
filled valence band and completely empty
conduction band. Depending on the magnitude
of the gap we can classify insulators and
semiconductors.
Insulators have relatively wide forbidden band gaps. For typical insulators the band gap Eg
> 7 eV. On the other hand, semiconductors have relatively narrow forbidden bands. For typical
semiconductors Eg ≤ 1 eV.
Questions:
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