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Lecture 18 Lecture 18 Quantum Theory of Extrinsic Semiconductors Suggested reading: 5.1-5.2
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Lecture 18 - Stanford University

Oct 24, 2021

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Page 1: Lecture 18 - Stanford University

Lecture 18Lecture 18

Quantum Theory of Extrinsic Semiconductors

Suggested reading: 5.1-5.2

Page 2: Lecture 18 - Stanford University

5 key semiconductor properties

1. Negative temperature coefficient of resistance conductivity increases with increasing

temperature

2. Photoconductivityresistivity depends on

5. Electroluminescencean applied voltage can resistivity depends on

the light intensityan applied voltage can

produce light

image from crunchgear.com

3. Photovoltaic effects 4. Rectification

image from allwin21.com image from instructables.com

light can produce current & voltage

resistance varies with the direction of current flow

Page 3: Lecture 18 - Stanford University

Silicon is the most important semiconductor in today’s electronics & photovoltaics (Images courtesy of IBM and Sunpower)

Page 4: Lecture 18 - Stanford University

Modern Si fabrication begins with wafer-pulling

200 mm and 300 mm Si wafers.SOURCE: Courtesy of MEMC, Electronic Materials, Inc. & Texas Instruments

Page 5: Lecture 18 - Stanford University

Si is sp3 hybridized and bonds with 4 neighbors

A simplified two-dimensional illustration of a Si atom with four A simplified two dimensional illustration of a Si atom with four hybrid orbitals hyb. Each orbital has one electron.

Page 6: Lecture 18 - Stanford University

Electrons in covelent bonds valence band

χ=electron affinity

Left: A simplified two‐dimensional view of a region of the Si crystal showing covalent bonds.

Right: The energy band diagram at absolute zero of temperature.

Page 7: Lecture 18 - Stanford University

How do electrons enter the conduction band?

A two-dimensional pictorial view of the Si crystal showing covalent bonds as two lines where each line is a valence electron.

Page 8: Lecture 18 - Stanford University

1: Photon excitation across the bandgap Eg

A photon with an energy greater than Eg can excite an electron from the VB to the CB.

Page 9: Lecture 18 - Stanford University

1: Photon excitation across the bandgap Eg

A photon with an energy greater than Eg can excite an electron from the VB to the CB.

When a photon breaks a Si-Si bond, a free electron and a hole in the Si-Si bond is created.

Page 10: Lecture 18 - Stanford University

2: Thermal excitation across the bandgap Eg

Thermal vibrations of atoms can also break bonds and thereby create electron-hole pairs.

Page 11: Lecture 18 - Stanford University

Electrons and holes

A pictorial illustration of a hole in the valence band wandering around the crystal due to the tunneling of electrons from neighboring bonds.

Page 12: Lecture 18 - Stanford University

Electron-hole recombination

An electron in the conduction band can “recombine” with a hole in the valence band, often emitting photons (“direct gap” semiconductors such as GaAs & InP)

or heat (“indirect gap” semiconductors such as Si & Ge) in the process.

Page 13: Lecture 18 - Stanford University

Conduction in semiconductors

Electron collisions

with thermal vibrationsvibrations

When an electric field is applied, electrons in the CB and holes in the VB can drift and contribute to the conductivity.

Applied field bends the energy bands since the electrostatic PE of the electron is –eV(x) and V(x) decreases in the direction of Ex, whereas PE increases.

Page 14: Lecture 18 - Stanford University

Both electrons and holes contribute to conduction

J=envde+epvdh

vde = eEx and vdh = hEx

J=current density

vd = drift velocity of the electrons vdh = drift velocity of the holesvde = drift velocity of the electrons, vdh = drift velocity of the holes

n=electron concentration in CB, p=hole concentration in VB

e = electron drift mobility, h = hole drift mobility, Ex = applied electric fielde d b y, h d b y, x pp d d

Page 15: Lecture 18 - Stanford University

Both electrons and holes contribute to conduction

J=envde+epvdh

vde = eEx and vdh = hEx

J=current density

vd = drift velocity of the electrons vdh = drift velocity of the holesvde = drift velocity of the electrons, vdh = drift velocity of the holes

n=electron concentration in CB, p=hole concentration in VB

e = electron drift mobility, h = hole drift mobility, Ex = applied electric fielde d b y, h d b y, x pp d d

Conductivity of a Semiconductor

d l h l h

= ene + eph

= conductivity, e = electronic charge, n = electron concentration in the CB

e = electron drift mobility, p = hole concentration in the VB, h = hole drift mobility

Page 16: Lecture 18 - Stanford University

f(E), g(E), and Carrier Concentrations

Page 17: Lecture 18 - Stanford University

Electron Concentration in the Conduction Band (CB)

dEEfEgdEn CBE )()(

nE= number of electrons per unit energy per unit volume in the conduction band

Page 18: Lecture 18 - Stanford University

Electron Concentration in the Conduction Band (CB)

dEEfEgdEn CBE )()(

nE= number of electrons per unit energy per unit volume in the conduction band

CE

dEnn CE

E dEnn

A E i l f kT b l E f(E) l k lik hAssume EF is at least a few kT below EC, so f(E) looks like the Boltzmann distribution:

f(E) ~ exp[-(E-EF)/kT]( ) p[ ( F) ]

Also, approximate upper limit of integral as infinity

Page 19: Lecture 18 - Stanford University

Electron Concentration in the Conduction Band (CB)

kTEENn Fc

c)(exp

n = electron concentration in the CB, Nc = temperature dependent constant, Ec = conduction band edge, EF = Fermi energy, k =

B l T

Boltzmann constant, T = temperature

Looks just like the Boltzmann Distribution Function, f(E)!

n ~ f(E)*g(E)

Page 20: Lecture 18 - Stanford University

Electron Concentration in the Conduction Band (CB)

kTEENn Fc

c)(exp

n = electron concentration in the CB, Nc = temperature dependent constant, Ec = conduction band edge, EF = Fermi energy, k =

B l T

Boltzmann constant, T = temperature

Effective Density of States at CB Edge

N 22me

*kT2

3 / 2

Nc = effective density of states at the CB edge, me* = effective mass of the electron in

Nc 2h2

c y g ethe CB, k = Boltzmann constant, T = temperature, h = Planck’s constant

Page 21: Lecture 18 - Stanford University

Hole Concentration in the Valence Band (VB)

kTEENp vF

v)(exp

p = hole concentration in the VB, Nv = effective density of states at the VB edge, EF = Fermi energy, Ev = valence band edge, k = Boltzmann constant, T = temperature

Effective Density of States at VB Edge

Nv 22mh

*kTh2

3 / 2

Nv = effective density of states at the VB edge, mh* = effective mass of a hole in the

VB k B lt t t T t t h Pl k’ t t

h

VB, k = Boltzmann constant, T = temperature, h = Planck’s constant

Page 22: Lecture 18 - Stanford University

Let’s consider the product of n and p:

kTE

NNnp gvc exp

kTvc

h d 2 h d d h lThe np product is a constant, ni2, that depends on the material

properties Nc, Nv, Eg, and the temperature.

If i i d ( b d i ) p t d t k p t t If n is increased (e.g. by doping), p must decrease to keep np constant.

We call ni the “intrinsic concentration”.

Mass action law applies in thermal equilibriumd i th d k ( ill i ti )and in the dark (no illumination)

Page 23: Lecture 18 - Stanford University

Electron-hole recombination & generation

The rate of recombination between electrons and holes is proportional to the concentration of carriers

Rate of recombination R ~ np

The rate of generation will depend on how many electrons are available for excitation at EV (i e NV) how many empty states are available for excitation at EV (i.e., NV), how many empty states are available at EC (i.e., NC), and the probability that the electron will

make the transition:

Rate of generation G ~ NV NC exp[-Eg/kT]

*** Thermal equilibrium: R = G ***