Chapter 2 Carrier Transport Phenomena
Chapter 2 Carrier Transport Phenomena
Chapter 2 Carrier Transport Phenomena
1. CARRIER DRIFT
Objective:
An electric field applied to a semiconductor will produce a force on
electrons and holes so that they will experience a net acceleration
and net movement, provided there are available energy states in the
conduction and valence bands. This net movement of charge due to
an electric field is called drift. The net drift of charge gives rise to a
drift current .
1. CARRIER DRIFT
According to quantum mechanics, electron have a free electron-like behavior and no
scattering occurs.
In real semiconductors, due to the imperfections, shown in the table, the electrons scatter,
which affects their transport (, , ) properties.
Important Sources of Scattering in Semiconductors
Ionized impurities
Phonons
Alloy
Interface roughness
Chemical impurities
Results in the Momentum & Energy of electrons will gradually lose coherence with the initial
state values. The average time it takes to lose coherence or memory of the initial state
properties is called (Mathiesons rule).
tot .sc
sc1 sc 2
...
sc = Scattering time or
Mean time between collisions for an electron or
Relaxation time or
Delay time
3
e.F . SC
vd
m*
F = = Electric Field
sc = scattering time
m* = effective mass
(either mn* or mo or mp*)
J = Current density
= drift current density
n = density of charge carrier
(either nn = n or np= p)
= conductivity of material
= resistivity of material = 1/
= mobility effects (factor)
(either n or p )
n.e2 . SC .F
J n.e.vd
m*
From Ohms Law,
J = .F
n.e2 . SC
n.e.
m*
From def. of mobility,
d = - .F (the e- move in a direction
opposite to the electric field while the
holes move in the same direction)
For general :
e. SC
m*
For e- :
e. .SC
n
mn *
For holes :
e. .SC
p
mp *
J e(nn .n n p . p ).F
Example 1
The mobility of e- in pure Si at 300 K is 1500 cm2/ V.s. Calculate the relaxation time.
Given: m* = 0.26 m0
Ans:
The time for pure Si:
SC
2.2
x
10
s
19
e
1.6 x10 C
Example 2
The mobility of e- in pure GaAs at 300 K is 8500 cm2/ V.s. Calculate the relaxation
time. If the GaAs sample is doped at Nd = 1017 cm-3, the mobility decrease to 5000
cm2/ V.s. Calculate the relaxation time due to ionized impurity scattering.
Given: Donor (n-type) doped = m* = 0.067 m0
(Note:the mobility, decreases with the increase in temp. in order to ionized
the dopants because as the temp. rises the atoms in the crystal vibrate with
greater amplitude. In other words, the electrons scatter from the dopants from
these vibrations and mobility decreases)
Ans:
The time for pure GaAs:
1
SC
3.24
x
10
s
19
e
1.6 x10 C
1.9
x
10
s
19
e
1.6 x10 C
Mathiesons rule:
1
2
SC
1
1
SC
1
imp
SC
imp
SC
4.6 x1013 s
6
Example 3
Consider 2 semiconductor samples, Si and GaAs. Both materials are doped n-type at
Nd = 1017 cm-3. Assume 50% of the donors are ionized at 300 K. Calculate the
conductivity of the samples. Compare this conductivity to the conductivity of
undoped samples.
Given:Pure or undoped density of state (n) for Si
ni = pi = n = p = 1.5 x 1010 cm-3
Pure or undoped density of state (n) for GaAs
ni = pi = n = p = 1.84 x 106 cm-3
n (Si)
= 1000 cm2/ V.s
p (Si)
= 350 cm2/ V.s
n (GaAs)
= 8000 cm2/ V.s
p (GaAs) = 400 cm2/ V.s
Ans:
undoped e(ni .n ni . p )
(1.6 x1019 C )(1.5x1010 cm3 ){(1000 350)}cm2 / V .s
3.24 x106 (cm)1
Conductivity for undoped GaAs:
Cont. Example 3
pdoped
pdoped
ni2
ndoped
ni2
ndoped
(1.5 x1010 )2
3
3 For Si (very small compared to ndoped)
4.5
x
10
cm
5 x1016
(1.84 x106 )2
5
3 For GaAs (very small compared to ndoped)
6.77
x
10
cm
5 x1016
8(cm)1
Conductivity for doped GaAs:
Almost zero
doped e(nn .n np . p )
(1.6 x1019 C){(5x1016 )(8000cm1 / V .s) (6.77 x105 )(400cm1 / V .s)cm1}
64(cm)1
8
Example 4
Consider a Si semiconductor at T = 300 K with an impurity doping
concentration of Nd = 1016 cm-3 and Na = 0. Calculate the drift current
density, J, for an applied field, = 35 V/cm.
Given: n (Si) = 1350 cm2/ V.s
p (Si) = 480 cm2/ V.s
Ans:
Since Nd > Na , the semiconductor is n-type at room temperature, we
can assume complete ionization:
The n = nn ~ Nd = 1016 cm-3 and p = np = 0
2.25
x
10
cm
n
1016
(1.6 x10
[4 Marks]
[4 marks]
[2 marks]
[2 marks]
10
Solutions:
a)
n q n n
p q p p
b)
n
0.1(cm)1
14
3
n
6.25
x
10
cm
qn (1.6 x1019 C )(1000cm2 / Vs)
p
0.1(cm)1
15
3
p
2.08
x
10
cm
q p (1.6 x1019 C )(300cm2 / Vs)
n
1 n
EFn EC k BT ln
N
N
8
C
C
EFn
19
19
(2.78
x
10
)
(2.78
x
10
)
8
p
1 p
EFp EV k BT ln
N
N
8
V
V
EFp
18
18
8 (9.84 x10 )
(9.84 x10 )
11
c) n exp EFn Ei
ni
k BT
d)
n E Ei
ln Fn
k BT
ni
n
6.25 x1014
EFn Ei k BT ln (0.026) ln
0.276eV
10
n
1.5
x
10
EC
0.278
EFn
0.276
Ei
0.3078
EFp
0.22
EV
Ei EFp
p
exp
ni
k
T
B
p Ei EFp
ln
k BT
ni
p
2.08 x1015
Ei EFp k BT ln (0.026) ln
0.3078eV
10
1.5 x10
ni
EgapBefore = 1.1 eV
EgapAfter = 0.276 + 0.3078 = 0.5838 eV
E = 1.1 - 0.5838 = 0.5162
12
13
(When > 100 kV/cm, the semiconductor suffers a breakdown in which current has
runaway behavior. The breakdown occurs due to carrier multiplication means the number
of electrons and holes that can participate in current flow increase. (The total number of
electrons conserved))
Conduction
band
Initial state
has 1 e-
Final state
has 2 e+ 1 hole
+
Valence
band
Avalanche process
14
dI ( z )
imp I
dz
I ( z)
N ( x)
exp( imp x)
I (O)
I = current
imp = Average rate of
ionization per unit
distance (coefficient
for e-)
imp = Average rate of
ionization per unit
distance (coefficients
for hole)
N = number of times an initial
electron will suffer impact
ionization after travelling
a distance x
T exp(
4 2m* Eg3/ 2
3e F
Electrons in
conduction
band
)
Available
empty states
(holes) in
valence
band
TGaAs exp(
3x(1.6 x10
19
C )(1.05 x10
34
Js)(2 x10 V / m)
)0
TInAs 3.7 x106 (means Zener Tunneling is important when ~2 x 105 V/m)
16
Figure 1
L
V
p-type semiconductor
Figure 2
18
(a) Refer to the Figure 1 (graph) above, determine and explain whether Zener Tunneling can
happen for the GaAs (electrons) at the time scattering between the range of:
5.00 x 10-8 s and 4.50 x 10-8 s.
[3 marks]
[3 marks]
(i)
(b) What assumption can you made as an electronic engineer from the graph above related to
the carrier drift velocity and the electric field for GaAs (Electrons)?
[3marks]
(c) Figure 2 shows a p-type semiconductor with applied voltage, V of 6.0 V and the length, L of
10.0 cm. Find the mobility of the holes in this semiconductor if the drift velocity is given as
2 x 107 cm/s.
[4 marks]
(d) An n-type Silicon sample with a resistivity of 10 cm at 300 K
(i)
[4 marks]
(ii) Calculate the Fermi level for n-type Si sample from the intrinsic Fermi level
[4 marks]
[4 marks]
[3 marks]
19
Answers:
2.1 X 107
Figure 1
3.4 X 103
First you need to find the scattering time of electrons at the maximum value of
carrier drift velocity with respect to the electric field for the GaAs (Electron). The
scattering time before this point will be considered at the low electric field region.
The scattering time after this point will be considered under high electric field and
can be solved thru Zener Tunneling and Avalanching breakdown theories only.
20
vd
SC
e.F . SC
me
3.52 108 s
19
3
e.F
(1.6 10 C )(3.4 10 V / cm)
(2.0 106 cm / s)
me vd 1
12
1 .
(5.7 10 ).
4.39 10 8 s
2
(2.6 10 V / cm)
e F1
6
me vd 2
12 (4.0 10 cm / s )
2 .
(5.7 10 ).
4.56 108 s
2
(5 10 V / cm)
e F2
(1.0 107 cm / s)
me vd 3
12
3 .
(5.7 10 ).
1.9 10 9 s
4
(3.0 10 V / cm)
e F3
(7.0 106 cm / s )
me vd 4
12
4 .
(5.7 10 ).
0.32 10 9 s
5
(1.25 10 V / cm)
e F4
Note: d the e- move in a direction opposite to the electric field while the holes move
in the same direction
3
(a i)No. From the calculation we can see that the scattering time is about 3.52 x 10 -8 s. Therefore any range that is bigger than
this value will consider that the Zener Tunneling is not happen yet.
3
(a ii)Yes. From the calculation we can see that the scattering time is 3.52 x 10 -8 s. Therefore any range that is smaller than
this value will consider that the Zener Tunneling will happen.
(b) After a certain point, or F around 3.4 x 103 V/cm, the vd start to slow down, showing that the voltage breakdown will
happen therefore we have to use Zener Tuneling or Avalanching breakdown theories to solve the problem.
3
21
(c ) p
v
v
10.0cm
L
v. (2 107 cm / s).
3.33 107 cm / V .s
F V L
6.0V
V
1 n
n
0.1(cm) 1
14
3
(d )(i )n
6.25
x
10
cm
q n q n (1.6 x1019 C )(1000cm 2 / Vs)
n
6.25 x1014
(d )(ii ) EFn Ei k BT ln (0.026) ln
0.276eV
10
1.5 x10
ni
(d )(iii )
2. CARRIER DIFFUSION
Objective:
There is a second mechanism, in addition to drift, that can induce a
current in a semiconductor. We can consider a classic physics
example in which a container as shown is divided into 2 parts by a
membrane. The left side contains gas molecules at a particular
temperature and the right side is initially empty. The gas molecules
are in continual random thermal motion so that, when the membrane
is broken, there will be a net flow of gas molecules into the right side
of the container. Diffusion is the process whereby particles flow from
a region of high concentration toward a region of low concentration. If
the gas molecules were electrically charged, the net flow of charge
would result in a diffusion current.
x= 0
2. CARRIER DIFFUSION
Arising from thermodynamics, when there is a gradient in the concentration of a species of
mobile particles, the particles diffuse from the regions of high concentration to the low
concentration.
Due to the random motion of the particles collision of various scattering processes
(remember, no ) in space.
Calculate the electron flux, ( x, t ) to the right across x = x0 at any instant of time, t.
( x, t )
But,
(nL nR )
2 SC
nL nR
dn
.
dx
Net Flux:
n ( x, t )
2 SC
dn( x, t )
dn( x, t )
Dn
dx
dx
for electron
dp( x, t )
p ( x, t ) Dp
dx
for hole
24
dn( x, t )
dp( x, t )
eDp
dx
dx
25
Example 7
Determine the carrier density gradient to produce a given diffusion current
density.
The hole concentration in silicon at T = 300 K varies linearly from x = 0 to x
= 0.01 cm. The hole diffusion coefficient is Dp = 10 cm2/s, the hole diffusion
current density is Jdif = 20 A/cm2, and the hole concentration at x = 0 is p = 4
x 1017 cm-3. Determine the hole concentration at x = 0.01 cm.
dn( x, t )
dp( x, t )
J tot (diff ) J n (diff ) J p (diff ) eDn
eDp
dx
dx
J dif
p( x)
p(0.01) p(0)
J p (diff ) eD p
eD p
x
0.01 0
17
p
(0.01)
(4
x
10
)
19
20 (1.6 x10 )(10)
0.01
Example 8
The electron concentration in silicon decreases linearly from 1016 cm-3 to
1015 cm-3 over a distance of 0.10 cm. The cross-sectional area of the
sample is 0.05 cm2. The electron diffusion coefficient is 25 cm2/s. Calculate
the electron diffusion current.
dn
n
J eDn
eDn
dx
x
15
16
10
10
19
J 1.6 x10 25
0.10 0
J 0.36 A / cm 2
J 0.36 A / cm 2
For A = 0.05 cm 2
I AJ 0.05 0.36 I 18 mA
27
Example 9
The hole concentration in silicon decreases linearly from 1015 cm-3 to 2x1014 cm-3 over a
distance of 0.10 cm (diffusion length). The cross-sectional area of this cylinder is 0.075
cm2. The hole diffusion coefficient is Dp = 10 cm2/s.
i) Calculate the hole diffusion current (Ip).
ii)Calculate the hole diffusion current density (Jp).
iii)Calculate the radius, r of the cross-sectional area of this cylinder.
iv)Calculate the scattering time, p for the hole.
v)How are you going to increase the current without increase the hole concentration?
(2 x1014 ) 1015
dp
19
i ) I p eD p A 1.6 x10 10 0.075
0.96 mA
dx
0.10
Ip
0.96mA
2
12.8
mA
/
cm
A 0.075cm 2
0.075
iii ) A r 2 0.075cm 2 r
0.15cm
ii ) J P
L
iv) LP D p p p P 1103 s
Dp
v)increase the ' r ', i.e (r 0.25 instead of 0.15) I p
0.96 mA
(0.25cm 2 ) 2.56mA
2
0.075cm
28
Example 10
The electron concentration in a sample of n-type silicon varies linearly from
1017 cm-3 at x = 0 to 6 x1016 cm-3 at x = 4 m. The electron current density is
experimentally measured to be -400 A/cm2. What is the electron diffusion
coefficient?
J n eDn
dn
dx
eDn
n
x
19
400 Dn 16
(6 x10 ) 10
Dn (4 x104 ) 0
16
17
Dn 25 cm / s
2
29
y mx c
0.1
0.1 eV
( EF Ei )eV
x
(0.1)
eV
5 m
eV
( EF Ei )eV 200
x (0.1)eV
cm
0
E Ei
200 x 0.1 Boltzman equation
n ni exp F
n
exp
i
k BT
k BT
x m
200 x 0.1
200 x 0.1
dn
d
200
n
exp
n
exp
i
i
dx dx
k BT
k BT
k BT
J n eDn
dn
dx
eDn
200 x 0.1
200
n
exp
i
k BT
k BT
19
10
J n (1.6 10 )(25)
(1.5
10
)
exp
(0.026)
0.026
J n (4.6 10
30
3. CARRIER INJECTION
Objective:
If electrons and holes are injected into a semiconductor, either by external contacts or by optical
excitation, the system is no more equilibrium. Now the system is called Quasi-Fermi levels
31
Example 12
Using Boltzmann statistics, calculate the position of the electron and hole
quasi-fermi levels when an e-h density of (n = p = 1017cm-3) is injected into
pure (undoped) Si. At 300 K.
Given: NC = 2.8 x 1019 cm-3, NV = 1.04 x 1019 cm-3, Eg (Si) = EC - EV = 1.12 eV
Electron Density
Hole Density
E Ec
E Ei
n NC exp Fn
ni exp F
kBT
kT
Ev EFp
p N v exp
k
T
Ei EF
ni exp
kT
Boltzmann approximation
For n or e-:
For holes or p:
n
EFn EC k BT ln
NC
p
EV EFp k BT ln
N
V
32
n
EFn EC k BT ln
N
C
EC
0.146 eV
EFn
1017
EFn k BT ln
EC ( EC 0.146)eV
EC (0.026) ln
19
N
2.8
x
10
C
EFp
p
EV kBT [ln
] ( EV 0.121)eV
NV
EFp
0.121 eV
EV
EFn - EFp = (EC EV) (0.146+0.121) = 1.12 0.267 = 0.853 eV
If we had injected only n = p = 1015cm-3 , the differences in the quasi-fermi
levels would be:
EFn - EFp = (EC EV) (0.266 + 0.24) = 1.12 0.506 = 0.614 eV
33
1.
2.
3.
Why does Fermi level shift toward conduction or valence band with doping?
The Fermi level is the energy separating occupied states (or levels) of the valence band from empty states
(levels) of the conduction band at the absolute temperature T=0 Kelvin. The Fermi level is an energy level
characteristic of the statistics (distribution law) which controls the occupation of any energy state by a
given particle: an electron or a hole in semiconductors. Electrons and holes are both fermion particles (
with half values of the spins) and both of them obey the Fermi-Dirac statistics which becomes
asymptotically the Boltzman statistics in dilute systems (with few electrons and or holes) or nondegenerate
systems. The position of the Fermi level with respect to valence and or conduction bands depends on
various parameters as the temperature, the effective masses of electrons and holes, and the number of
free electrons and holes. This variation of the Fermi level obeys two condictions : - the ''mass action law''
which states that the number of particles of each type as well as the overall number of the particles must
conserve whatever is their distribution on the available energy levels. - The neutrality equation which states
that the electrical neutrality has to be fulfilled, i.e. the number of negative charges must be
counterbalanced excatly by the same number of positive charges. 2.
In an intrinsic semiconductor (with no doping at all), the Fermi level is lying exactly at the middle of the
energy bandgap at T=0 Kelvin. With increasing temperature T>0 Kelvin the Fermi energy remains at this
midgap position if conduction and valence bands have exactly the same dispersion energy or more simply
the same effective masses for electrons and holes. If not then the Fermi level will shift away from midgap
position with increasing temperature and will move towards the band with the smaller effective mass
In an extrinsic semiconductor (with added doping), in order to conserve the number of particles (mass
action law) and to fulfill the overall electrical charge neutrality (neutrality equation), the Fermi level has to
move away from the midgap position. It has to shift towards conduction band in an n-type
semiconductor (extrinsic semiconductors with added doping impurities which are donors i.e.
impurities which give additional electrons to the system) where the number of electrons n is higher than the
number of holes (n>p). It shifts towards valence band in a p-type semiconductor (extrinsic semiconductors
with added doping impurities which are acceptors i.e. impurities which trap electrons from the system
giving rise to a deficit of electrons or an excess of holes ) where the number of electrons n is lower than the
number of holes (n<p)
34
0.228
10
14
3
(1.5
x
10
)
exp
1.01466
x
10
cm
0.025852
2.21749 x106 cm 3
14
n 1.01466 x10
Note :
( EFn EFi ) EFi EFn 0.228eV
b) Find the intrinsic Fermi level for the majority and minority carrier
density (use the value of n & p from part a)).
n
EFn EFi ( EFi EFn ) k BT ln
ni
1.01466 x1014
(0.025852) ln
0.228eV
10
1.5 x10
Majority (from n)
p
EFi EFp ( EFp EFi ) k BT ln
ni
2.21749 x106
(0.025852) ln
0.228eV
10
1.5 x10
Minority (from p)
Note: same value of energy, i.e 0.228 eV, why? Because we are trying to find the
same level of energy but using different charge carriers, i.e n and p.
c) Find the Fermi level for the majority and minority carrier density
by using Joyce-Dixon approximation.
n
1 n
EC EFn k BT ln
N
N
8
C
C
19
19
(2.78
x
10
)
(2.78
x
10
)
8
n
1 n
EC EFn k BT ln
N
N
8 i
i
10
10
(1.5
x
10
)
(1.5
x
10
)
8
EC
0.3236 eV
EFn
0.228 eV
EFi
EFp
0.7528 eV
EV
38
Figure 10
Figure 11
(a)
(b)
(c)
Now, we have
Generation via a trapping
center: (1) an electron is
elevated from the valence
band into the trap creating a
free hole and then (2) the
electron is elevated into the
conduction band creating a
free electron
or,
Recombination via a
trapping center: (a)(1)an
electron is trapped and then
(2) a hole is trapped; (b)(1)
or hole is trapped and then
(2) an electron is trapped;
(c)(1)or an electron is
trapped and then (2) the
electron falls into an empty
state (hole)
40
n
p
n
R
=
R
0 0
i
G
R
RR = the carrier recombination rate
n = Total electron (may be functions of time or position)
p = Total hole (may be functions of time or position)
n0 =Thermal equilibrium electron concentration (independent of time and position)
p0 = Thermal equilibrium hole concentration(independent of time and position)
ni = Intrinsic concentration
np n0 p0 ni2
41
Creation of excess
electron and hole
densities by photons in
Generation process
Recombination of
excess carriers
reestablishing thermal
equilibrium
42
43
Conduction
band
-
Photon
Vertical in k
Photon
+
Valence
band
Photon Absorption
Photon Emission
Carrier lifetime = n 0 or p 0
Excess electron concentration = n
n n0
p p p0
May be functions
of time or position
Example 1
Excess electrons have been generated in a
semiconductor to a concentration of n(0) 1015 cm3
6
The excess carrier lifetime is n 0 10 s . The
forcing function generating the excess carriers
turns off at t = 0 so the semiconductor is
allowed to return to an equilibrium condition
for t>0. Calculate the excess electron
concentration for
t
n(t ) n(0) exp( )
a) t=0
n0
n 1015 cm3
b) t=1s
t
n(t ) 10 exp(
)
1 s
n 3.68x1014 cm3
c) t=4s
n 1.83x1013 cm3
15
n(0)
Carrier
Injection
n( x )
n( x L)
Example 14
Find the recombination rate of the excess electrons for example 1.
n(t ) p(t )
R
p0
n0
1015
a) R 6 1021 cm3 s 1
10
14
3.68
x
10
20
3 1
b) R
3.68
x
10
cm
s
6
10
1.83x1013
c) R
1.83x1019 cm3 s 1
6
10
Note:
1. When excess electron density ( n ) is injected in p-type material. This excess minority
carriers (n ) will recombine with the majority carriers (p ) with a rate given by:
n(t )
n0
2. When excess holes density ( p ) is injected in n-type material. This excess minority
carriers (p ) will recombine with the majority carriers ( n) with a rate given by:
p(t )
p0
46
Dn n or Dp p
Example 15
Electrons are injected into a p-type silicon sample at 300 K with the carrier lifetime is given
by 5x10-9s. The excess electrons have been generated in a semiconductor to a concentration
of n(0) 1012 cm3 .
a) Calculate the rate of the recombination of the excess electron (excess minority carriers
( n) ) in a p-type silicon at t = 0 s.
b) Calculate the diffusion length for the electrons if the diffusion coefficient is 30 cm2/s at
i) t = 0 s, ii) t = 3 x 10-9 s, t = 4 x 10-9 s
Ans:
a)
n(t ) (1x1012 )
20
3 1
R
2
x
10
cm
s
9
n 0 (5 x10 )
Example 16
Consider a semiconductor in which n0 1015 cm3 and ni 1010 cm3 . Assume
that the excess carrier lifetime is 106 s . Determine the electron-hole
recombination rate if the excess hole concentration is p 5x1013 cm3 .
n-type semiconductor, low-injection so that
p
pO
13
5 x10
10
R 5 x10 cm s
19
3 1
48
Total rate of particle flow = Particle flow due to current (Loss due to
recombination rate + Gain due to generation rate)
Particle Current
Loss
Gain
49
Design a uniformly doped p-type Germanium semiconductor bar with circular cross
sectional area. The semiconductor should provide a current of 3 mA under a bias
voltage of 6V. The maximum current density is to be 200 A/cm2. You are required
to provide the following information to the device production team:
(a) The required cross sectional area.
[3 marks]
(b) The resistance of the semiconductor bar.
[3 marks]
(c) The chosen doping concentration (refer to Figure 1 below) and the required
length.
[4 marks]
(a) A = I/Jdrift = 3 mA / 200 A/cm2 (1) =1.5 x 10-5 cm2 (2)
(b) R = V/I = 6 V / 3 mA (1) = 2 k (2)
(c) R = L / e p Na A (1)
[Any reasonable Na is acceptable. If Na is 1016cm-3, p 1400 cm2/Vs (from Figure 1). (1)]
L = e.p.Na.A.R = (1.6 x 10-19) . (1400) . (1016) . (1.5 x 10-5) . (2 k) = 6.72 x 10-2 cm (2)
(1400)
(1016)
Figure 1. Electron and hole mobility versus impurity concentrations for germanium,
silicon and gallium arsenide at T=300K
52
[6 marks]
(b) As a design engineer, what can you conclude if the value of E exceed 500 kV/cm and also what is the value of
breakdown voltage, VB at the doping concentration of 3x1012 cm-3.
[4 marks]
53
J
(2.56 x107 Acm 2 )
7
1
(a )vd
8
x
10
cm
.
s
(3)
18
3
19
n.e (2 x10 cm ).(1.6 x10 C )
(8 x107 cm.s 1 )
5
E
(4
x
10
V / cm)(2)
2
2
(2 x10 cm / V .s )
E is not exceeded 500kV/cm.(1)
vd
(b) If E exceed 500kV/cm, it means that the breakdown voltage will happen
therefore we have to use Zener Tunneling or Avalanching Breakdown
theories to solve the problem.(2)
S .E 2
2.7
10
V
19
12
-3
2.e.N B
2.(1.6 x10 C ).(3 10 cm )
note: the value of VB 2.7 105V (2)
54
8V
vd e.F . sc e. sc q.
F
me .F
me
me
(2)
1312
m
/ Vs (3)
30
0.067 (0.9110 )
V
vdrift n E n (2)
L
8V
vdrift (1312 m 2 / Vs )(
) 2624 00 m / s 2.624 107 cm / s (3)
0.04m
55
Ld
V /F
(5V ) /(8V / cm)
d .R.N d .q V
(3900cm 2 / Vs). 5V (5.0 1018 cm 3 )(1.6 1019 C )
.
.
N
.
q
dI d
0.5 A
5+2
0.625cm
5
2
A
2.0 10 cm
1
31200cm
Ld
A r 2 (if r )
d .R.N d ().q
N d will decrease
2+1
56