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Solid State Physics

Types of Solids
Ionic, Covalent, and Metallic.

Classical Theory of Conduction

Current density j, drift velocity vd, resistivity

Band Theory and Band Diagrams


Energy levels of separated atoms form energy band
when brought close together in a crystal.
Fermi Function for how to fill bands.
Metal, Insulator, and Semiconductor band diagrams.
Donor and Acceptor dopants (Hall Effect).

Devices
pn junction, diode

Types of Solids
Ionic, Covalent, and
Metallic

Types of Solids: Ionic Solid Properties

Formed by Coulombic attraction between ions.


Examples include group I alkali cations paired with group
VII halide anions, e.g. Na+ Cl-.

Large cohesive energy (2-4 eV/ atom).


Leads to high melting and boiling points.

Low electrical conductivity.


No free electrons to carry current.

Transparent to visible light.


Photon energy too low to free electrons.

Soluble in polar liquids like water.


Dipole of water attracts ions.

Types of Solids: Ionic Solid Crystal Spacing


Repulsive Potential 1/rm
Total Potential

Attractive Coulombic
Potential -1/r

Potential Energy: Utot = Uattract (+,) + Urepulse (, )

Types of Solids: Covalent Solid


Examples include group IV elements (C, Si) and III-V
elements (GaAs, InSb).
Formed by strong, localized bonds with stable, closedshell structures.
Larger cohesive energies than for ionic solids (4-7
eV/atom).
Leads to higher melting and boiling points.

Low electrical conductivity.


Due to energy band gap that charged carriers must
overcome in order to conduct.

Types of Solids: Metals


Formed by Coulombic attraction between (+) lattice ions and
() electron gas.
Metallic bonds allows electrons to move freely through
lattice.
Smaller cohesive energy (1-4 eV).
High electrical conductivity.
Absorbs visible light (non-transparent, shiny due to reemission).
Good alloy formation (due to non-directional metallic bonds).

Classical Theory of Conduction

Classical Theory of Conduction


Macroscopic
dq
Current: i
(Amps)
dt

q idt
V
i
R

L
R
A

Microscopic
v di
Current Density: J v (A/m 2 )
dA

v v
i J dA

ur Ev
v
J E where resistivity

r
r
J n e vd

m
2

ne

Drift velocity vd is net motion of electrons (0.1 to 10 -7 m/s).


Scattering time is time between electron-lattice collisions.

conductivity
where n carrier density
vd drift velocity
where scattering time

Classical Theory of Conduction: Electron Motion

Electron travels at fast velocities for a time and then collides


with the crystal lattice.
Results in a net motion opposite to the E field with drift velocity
vd.
Scatter time decreases with increasing temperature T, i.e. more
scattering at higher temperatures (leads to higher resistivity).

Classical Theory of Conduction:


Resistivity vs. Temp.

FE

ma

E
m
1
e
e

J
ne vd
ne (a )
n
ne 2
Metal:

Resistance increases with Temperature.

Why? Temp , n same (same # conduction


electrons)
Semiconductor: Resistance decreases with Temperature.
Why? Temp , n (free-up carriers to conduct)

Band Theory: Two Approaches

Band Theory: Two Approaches


There are two approaches to finding the electron energies
associated with atoms in a periodic lattice.
Approach #1: Bound Electron Approach (single atom
energies!)
Isolated atoms brought close together to form a solid.

Approach #2: Unbound or Free Electron Approach (E =


p2/2m)
Free electrons modified by a periodic potential (i.e. lattice
ions).

Both approaches result in grouped energy levels with


allowed and forbidden energy regions.
Energy bands overlap for metals.
Energy bands do not overlap (or have a gap) for
semiconductors.

Band Theory: Bound Electron Approach


For the total number N of atoms in a solid (1023 cm3),
N energy levels split apart within a width E.
Leads to a band of energies for each initial atomic
energy level (e.g. 1s energy band for 1s energy level).
Two atoms

Six atoms

Solid of N atoms

Electrons must occupy different energies due to Pauli


Exclusion principle.

Band Diagram: Fermi-Dirac Filling Function

Band Diagram: Fermi-Dirac Filling Function


Probability of electrons (fermions) to be found at various energy levels.

f FD E

E EF

kT

At RT, E EF = 0.05 eV f(E) = 0.12


E EF = 7.5 eV f(E) = 10 129

1 Exponential dependence has HUGE


effect!

Temperature dependence of Fermi-Dirac function shown as follows:

Step function behavior smears out at higher temperatures.

Band Diagram: Metal


T>0
EC,V

Fermi filling
function
Conduction band
(Partially Filled)

EF

Energy band
to be filled

E=0

At T = 0, all levels in conduction band below the Fermi energy EF


are filled with electrons, while all levels above EF are empty.
Electrons are free to move into empty states of conduction band
with only a small electric field E, leading to high electrical
conductivity!
At T > 0, electrons have a probability to be thermally excited
from below the Fermi energy to above it.

Band Diagram: Insulator


T>0

Conduction band
(Empty)

EC

Egap

EF
Valence band
(Filled)

EV

At T = 0, lower valence band is filled with electrons and upper


conduction band is empty, leading to zero conductivity.
Fermi energy EF is at midpoint of large energy gap (2-10 eV)
between conduction and valence bands.
At T > 0, Thermal electrons are usually NOT able to overcome the
energy gap, leading to zero conductivity.

Band Diagram: Semiconductor with No Doping


T>0

Conduction band
(Partially Filled)

EC
EF
EV

Valence band
(Partially Empty)

At T = 0, lower valence band is filled with electrons and


upper conduction band is empty, leading to zero
conductivity.
Fermi energy EF is at midpoint of small energy gap (<1 eV)
between conduction and valence bands.

At T > 0, electrons thermally excited from valence to


conduction band, leading to measurable conductivity.

Band Diagram: Donor Dopant in Semiconductor


Increase the conductivity of a semiconductor by adding a small
amount of another material called a dopant (instead of heating it!)

For group IV Si, add a group V


element to donate an electron
and make n-type Si (more
EC
negative electrons!).
ED
Extra electron is weakly bound,
with donor energy level ED just
EV
below conduction band EC.
Dopant electrons easily promoted
to conduction band, increasing
electrical conductivity by
increasing carrier density n.

Fermi level EF moves up towards EC.

n-type Si

EF
Egap~ 1 eV

Band Diagram: Acceptor Dopant in Semiconductor

For Si, add a group III element


to accept an electron and
make p-type Si (more positive
holes).
Missing electron results in an
extra hole, with an acceptor
energy level EA just above the
valence band EV.
Holes easily formed in valence
band, greatly increasing the
electrical conductivity.

Fermi level EF moves down


towards EV.

EC

EV

EA
EF
p-type Si

pn Junction: Band Diagram


Due to diffusion, electrons
move from n to p-side and
holes from p to n-side.
Causes depletion zone at
junction where immobile
charged ion cores remain.
Results in a built-in
electric field (103 to 105
V/cm), which opposes
further diffusion.
Note: EF levels are aligned
across pn junction under
equilibrium.

pn regions touch & free carriers


move

EC
EF
EV

n-type electrons

EF
holes

p-type

pn regions in equilibrium
EC
EF
EV

+
+
+ +

+ ++
+ ++
++
Depletion Zone

pn Junction: IV Characteristics
Current-Voltage
Relationship

I I o [e

eV / kT

1]

Forward Bias: current


exponentially increases.
Reverse Bias: low
leakage current equal to
~Io.
Ability of pn junction to
pass current in only one
direction is known as
rectifying behavior.

Forward
Bias

Reverse
Bias

pn Junction: Band Diagram under Bias


Forward Bias: negative voltage on n-side promotes diffusion of
electrons by decreasing built-in junction potential higher current.
Reverse Bias: positive voltage on n-side inhibits diffusion of electrons
by increasing built-in junction potential lower current.
Equilibrium

p-type

n-type

Forward Bias

p-type

Reverse Bias

n-type

p-type

n-type

e
Majority Carriers

+V

e
Minority Carriers

Semiconductor: Dopant Density via Hall Effect


Why Useful? Determines carrier type (electron vs. hole) and
carrier density n for a semiconductor.
How? Place semiconductor into external B field, push
current along one axis, and measure induced Hall voltage
VH along perpendicular axis.
Carrier density n =
(current I) (magnetic field B)
(carrier charge q) (thickness t)(Hall voltage VH)

Derived from Lorentz equation


FrE (qE) = FB (qvB).
r
r
Hole
Electron
FB qv B
+ charge

charge

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