Skip to content
Snippets Groups Projects
search:
  exclude: true
from matplotlib import pyplot as plt 
import numpy as np
from math import pi

Solutions for lecture 13 exercises

Exercise 1: Energy, mass, velocity and cyclotron motion of electrons and holes

Question 1.

Electrons near the top of the valence band have a negative effective mass, their energy decreases as

kk
increases from 0, and they have a negative group velocity for
k>0k>0
.

Question 2.

Holes near the top of the valence band have a positive effective mass, their energy increases as

kk
increases from 0, and they have a negative group velocity for
k>0k>0
.

Question 3.

The equation of motion for an electron near the bottom of the conduction band is:

mdvdt=ev×B m^* \frac{d\mathbf{v}}{dt} = -e\mathbf{v} \times \mathbf{B}

and when replacing we get two coupled equations:

\begin{align} \dot{k_x} &= -\frac{e}{m^}B k_y\ \dot{k_y} &= +\frac{e}{m^}B k_x \end{align}

The solution to this equation is circular motion of cyclotron frequency of

ωc=eBm\omega_c = \frac{eB}{m^*}
, where the Lorentz force is perpendicular to
kE\nabla_\mathbf{k} E
.

Question 4.

A hole near the bottom of the conduction band will have the same chirality as an electron. The chirality would be just the opposite if we would consider the valence band (for both electrons and holes).

Exercise 2: The Hall coefficient when both electrons and holes are present in the system

Question 1.

RH,h=1ne R_{H,h} = \frac{1}{ne}

Question 2.

Filling in

ne=nhn_e = n_h
and
μe=μh\mu_e=\mu_h
results in
RH=0R_H = 0
.

Exercise 3. Holes and electrons in a 1D tight-binding energy band

Question 1.

For electrons we find

me=22ta2cos(ka) m_e = -\frac{\hbar^2}{2ta^2\cos(ka)}

ve=2tasin(ka), v_e = -\frac{2ta\sin(ka)}{\hbar},

and for holes we obtained

mh=me m_h = -m_e

vh=ve. v_h = v_e.

Thus the effective masses of electrons an hole will be of opposite sign, while the group velocities will be the same!

Question 2.

The number of holes is defined as

Nh=ε2tε+2tf(Eh,EF,h)gh(Eh)dEh, N_h = \int_{-\varepsilon-2t}^{-\varepsilon+2t} f(E_h, E_{F,h}) g_h(E_h)d E_h,

where

gh(Eh)g_h(E_h)
is the density of states of the holes in terms of hole energy
EhE_h
.

Question 3.

??? hint "Small hint"

It is convenient to write the hole integral in terms of the electron energy. 

Exercise 4: a 1D semiconductor

def dispersion(EG, tcb, tvb, N=100, kmax=np.pi/2):
    a = 1
    kx = np.linspace(-kmax, kmax, N)
    Ecb = EG - 2*tcb*(np.cos(kx*a)-1)
    Evb = 2*tvb*(np.cos(kx*a)-1)
    
    # Plot dispersion
    plt.figure(figsize=(6,5))
    cb, = plt.plot(kx, Ecb, label="Conduction B.")
    vb, = plt.plot(kx, Evb, label="Valence B.")

    plt.xlabel('$k_x$', fontsize=20)
    plt.ylabel('$E$', fontsize=20)
    plt.title('E(k) for tcb:'+str(tcb)+' tvb:'+str(tvb))
    plt.legend(handles=[cb, vb])

dispersion(10, 2, 8)

Question 1.

For the electrons in the conduction band we find

vcb,e=2atcbsin(ka) v_{cb,e} = \frac{2at_{cb}}{\hbar}\sin (ka)

mcb,e=22a2tcbcos(ka). m_{cb,e} = \frac{\hbar^2}{2a^2t_{cb}\cos (ka)}.

For the holes in the valence band we obtain

vvb,h=2atvbsin(ka) v_{vb,h} = -\frac{2at_{vb}}{\hbar}\sin (ka)

mvb,h=22a2tvbcos(ka). m_{vb,h} = -\frac{\hbar^2}{2a^2t_{vb}\cos (ka)}.

Question 2.

This approximation indicates the chemical potential is "well below" the conduction band and "well above" the valence band. This way, only a few electrons occupy the the states near the bottom of the conduction band and only a few holes occupy the states near the top of the valence band. This allows us the approximate the bottom of the conduction band and the top of the valence band as parabolic dispersions. In addition, the Fermi-Dirac distribution can be approximated as the Boltzman distribution.

The dispersions of the valence and conduction band are approximately equal to

EcbEG+tcb(ka)2 E_{cb} \approx E_G + t_{cb}(ka)^2

Evbtvb(ka)2 E_{vb} \approx -t_{vb}(ka)^2

Question 3.

For the density of states for both the electrons and holes we find

ge(E)=1πatcb(EEG),ifE>EG, g_e(E) = \frac{1}{\pi a \sqrt{t_{cb}(E-E_G)}}, \:\: \text{if} \:\: E > E_G,

and

gh(Eh)=1πatvbEh,ifEh>0, g_h(E_h) = \frac{1}{\pi a \sqrt{t_{vb}E_h}}, \:\: \text{if} \:\: E_h > 0,

where

Eh=EE_h = -E
.

Question 4.

The electron density in the conduction band is given by

\begin{align} n_e &= \int_{E_G}^{\infty} f(E)g_c(E)dE\ &\approx \int_{E_G}^{\infty} e^{-\beta (E-\mu)} g_c(E) dE\ &=\sqrt{\frac{k_B T}{\pi t_{cb}}}\frac{e^{\beta (\mu - E_G)}}{a}. \end{align}

Analoguous, we find for the hole density

\begin{align} n_h &= \int_{0}^{\infty} f(E_h) g_h(E_h) dE_h\ &\approx \sqrt{\frac{k_B T}{\pi t_{vb}}}\frac{e^{-\beta \mu}}{a}. \end{align}

Question 5.

In the intrinsic regime

ne=nhn_e = n_h
. Solving this for
μ\mu
results in

μ=12EG+kBT4ln(tcbtvb) \mu = \frac{1}{2}E_G + \frac{k_B T}{4}ln(\frac{t_{cb}}{t_{vb}})