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Overview
u
x
+
Vibrating Cu ions V
(a) (b)
(a) A conduction electron in the electron gas moves about randomly in a metal (with a mean speed
u) being frequently and randomly scattered by thermal vibrations of the atoms. In the absence of
an applied field there is no net drift in any direction.
(b) In the presence of an applied field, Ex, there is a net drift along the x-direction. This net drift
along the force of the field is superimposed on the random motion of the electron. After many
scattering events the electron has been displaced by a net distance, x, from its initial position
toward the positive terminal
𝑚2
𝜇 ≡ 𝑒𝑙𝑒𝑐𝑡𝑟𝑜𝑛 𝑚𝑜𝑏𝑢𝑙𝑖𝑡𝑦 [ ]
𝑠𝑣
Note: the current density is proportional to the electric field and the
conductivity 𝜍 is the term multiplying 𝐸𝑥 ,
𝜎𝑎𝑐
b) Find as function of frequency, 𝜔
𝜎𝑑𝑐
c) Find 𝜍𝑎𝑐, f = 50Hz, 106Hz ,1014Hz
𝑑𝑣𝑑 𝑣𝑑
𝐹 = −𝑒𝐸𝑥 = 𝑚 +𝑚
𝑑𝑡 𝜏
Sem. I, 2016/17 Electrical Engineering Materials – Chapter 2 19
Density of States and Fermi Dirac function
(b)
Fig 4.2
From Principles of Electronic Materials and Devices, Third Edition, S.O. Kasap (© McGraw-Hill, 2005)
i( )
i() R C
(a) v() L
0
Coupling
M i( )
i() R C C
(b) L L R
1 2
There is one resonant frequency, 0, in an isolated LCR circuit. (b) There are
two resonant frequencies in two coupled LCR circuits. One below and the
other above 0.
Fig 4.4
From Principles of Electronic Materials and Devices, Third Edition, S.O. Kasap (© McGraw-Hill, 2005)
E
E(R) SYSTEM
(a) E1s 1s 2 H-Atoms
0 2 Electrons
Bonding 1 Electron/Atom
Energy E(R) 1 Orbital/Atom
E(a)
R, Interatomic
0 a R= Separation
E
E1s E1s
E = Bonding Energy
(b) E
H -atom H2 H -atom
Electron energy in the system comprising two hydrogen atoms. (a) Energy of
and vs. the interatomic separation, R. (b) Schematic diagram
showing the changes in the electron energy as two isolated H atoms, far left
and far right, come to form a hydrogen molecule.
Fig 4.3
From Principles of Electronic Materials and Devices, Third Edition, S.O. Kasap (© McGraw-Hill, 2005)
E
E1s E1s
E
He-atom He-He He-atom
System
Fig 4.5
From Principles of Electronic Materials and Devices, Third Edition, S.O. Kasap (© McGraw-Hill, 2005)
E
a
c
Ec
Symmetric
A B C
c
b b System
Eb in isolation
Antisymmetric b E1s 3 H-Atoms
a 3 Electrons
Ea
c a 3 Orbitals (1s)
6 States (with spin)
Symmetric
Separation
R=a R=
(a ) (b)
(a) Three molecular orbitals from three 1s atomic orbitals overlapping
in three different ways. (b) The energies of the three molecular orbitals
labeled as a, b and c in a system with 3 H atoms (highly simplified).
Fig 4.7
From Principles of Electronic Materials and Devices, Third Edition, S.O. Kasap (© McGraw-Hill, 2005)
Review on Band Theory
System of N Li Atoms
Electron Energy in the System
solid(N) 2p
ET E2p
EMPTY
SYSTEM
N Li Atoms
E2s N Electrons
of N Li Atoms
2s
FULL
N Orbitals
2N States
EB solid(1)
E1s
Interatomic 1s
a Separation (R)
Solid Isolated Atoms
The formation of a 2s-energy band from the 2s-orbitals when N Li atoms
come together to form the Li solid. The are N 2s-electrons but 2N states in
the band. The 2s-band therefore is only half full. The atomic 1s orbital is
close to the Li nucleus and remains undisturbed in the solid. Thus each Li
atom has a closed K-shell (full 1s orbital).
Free electron
E = 0 (Vacuum Level)
EMPTY E3s
Electron energy
E 2p
E2s
FULL
E 1s
Interatomic
Separation (R)
R=a R=
The Solid Isolated Atoms
As solid atoms are brought together from infinity, the atomic orbitals
overlap and give rise to bands. Outer orbitals overlap first. The 3s
orbitals give rise to the 3s band, 2p orbitals to the 2p band and so on.
The various bands overlap to produce a single band in which the energy
is nearly continuous.
E Overlapping
Free electron
energy bands
E=0
3s Vacuum level
E lectron E nergy
2p 3p
3s
2s 2p
Electrons 2s
1s 1s
Solid Atom
Typical electron energy band diagram for a metal All the valence electrons
are in an energy band which they only partially fill. The top of the band is
the vacuum level where the electron is free from the solid (PE = 0).
3N
2/3
h2
EF
8m
When temperature increases, the Fermi level or Fermi
energy also slightly decreases.
When E< < EF (i.e.,) for energy levels lying below EF,
(E –EF) is a negative quantity and hence,
1 1
f(E)
1
1 e 1 0
That means all the levels below EF are occupied by
the electrons.
Electrical Engineering Materials – Chapter 2
Fermi Dirac distribution function at different temperatures
1
∆ (𝑠𝑒𝑝. 𝑏𝑛. 𝑙𝑒𝑣𝑒𝑙𝑠) ∝
𝑖𝑛𝑡𝑒𝑟𝑎𝑐𝑡𝑖𝑜𝑛 𝑏𝑛. 𝑎𝑡𝑜𝑚𝑠
(a) In the solid there are N atoms and N extended electron wavefunctions
from 1 all the way to N . There are many wavefunctions, states, that
have energies that fall in the central regions of the energy band. (b) The
distribution of states in the energy band; darker regions have higher
number of states. (c) Schematic representation of the density of states
g(E) vs. energy E.
is difficult!!;
Hence, Recall that in a cube an electron has an energy of
2
3
ћ 2 n1 = 1
𝐸𝑛 = 2n 2
8𝑚𝑑 n2 = 3
1
-n1 n1
0 1 2 3 4 5 6
-n2 n1 = 2, n2 = 2
This area is
• Taking Spin in to
n' consideration; the total no.
d) The number of states per unit volume within a small energy range
of kT to 2kT from the bottom of the band.
4 E1+E2 = E3 +E4
2
Interaction E4 (Energy Conservation)
E2
1 If 𝑃(𝐸1) the
3 probability of
E1
E3
Occupancy ;
The probability
Two electrons initially with wavefunctions 1 and 2 at E1 and E2
that it`s vacant 1-
interact and end up at different energies at E3 and E4. Their
corresponding wavefunctions are 3 and 4. 𝑃(𝐸1)
1 − 𝑃 𝐸3 𝑃 𝐸1 ∗ 𝑃 𝐸2 1 − 𝑃 𝐸4 = [1 − P(E1)]P(E3) ∗ P(E4)[1 − P(E1)]
1 1 1 1
−1 . −1 = −1 . −1 𝐴𝑒 𝛽𝐸
𝑃 𝐸1 𝑃 𝐸2 𝑃 𝐸3 𝑃 𝐸4
exp(-E/kT)
E2
E1
0 N(E)
N1 N2
EF +
n E
dE n
TK 0
EF
EF
g(E) = A E1/2
0
(a ) (b) (c ) (d)
3 1
∞ 8𝜋 2𝑚𝑒 2 ∞ 𝐸2
𝑛= 𝑔 𝐸 . 𝑓 𝐸 𝑑𝐸 = 0 1+exp(𝐸−𝐸𝑓
𝑑𝐸 ;
0 ℎ2 𝐾𝑇)
ℎ2 3𝑛 2/3
𝐸𝑓 = …. Large for good conductors;
8𝑚 𝜋
𝜋2 𝑘𝑇 2
𝐸𝑓 𝑇 = 𝐸𝑓0 1 − ;
12 𝐸𝑓0
Thermal Energy:
electrons absorb heat & transfer it due to collusion
c. Relaxation time