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Carrier drift
Current carriers (i.e. electrons and holes) will move under the influence of an electric field
because the field will exert a force on the carriers according to
F = qE
In this equation you must be very careful to keep the signs of E and q correct. Since the carriers
are subjected to a force in an electric field they will tend to move, and this is the basis of the drift
current. Figure illustrates the drift of electrons and holes in a semiconductor that has an electric
field applied. In this case the source of the electric field is a battery. Note the direction of the
current flow. The direction of current flow is defined for positive charge carriers because long
ago, when they were setting up the signs (and directions) of the current carriers they had a 50:50
chance of getting it right. They got it wrong, and we still use the old convention! Current, as you
know, is the rate of flow of charge and the equation you will have used should look like
Id = nAVdq
where
Id = (drift) current (amperes),
n = carrier density (per unit volume)
A = conductor (or semiconductor) area,
vd = (drift) velocity of carriers,
q = carrier charge (coulombs)
which is perfectly valid. However, since we are considering charge movement in an electric field
it would be useful to somehow introduce the electric field into the equations. We can do this via a
quantity called the mobility, where
d = E
In this equation:
= the drift mobility (often just called the mobility) with units of cm2V-1s-1
E = the electric field (Vcm-1)
We know that the conduction electrons are actually moving around randomly in the metal, but we
will assume that as a result of the application of the electric field Ex, they all acquire a net
velocity in the x direction. Otherwise, there would be no net flow of charge through area A.
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The average velocity of the electrons in the x direction at time t is denoted Vdx(t). This is called
the drift velocity, which is the instantaneous velocity Vx in the x direction averaged over many
electrons (perhaps, 1028 m-3); that is
Δq enAVdx Δt
Jx = = enVdx
AΔt AΔt
This general equation relates Jx to the average velocity Vdx of the electrons. It must be appreciated
that the average velocity at one time may not be the same as at another time, because the applied
field, for example, may be changing: Ex=Ex(t). We therefore allow for a time-dependent current
by writing
Jx(t) = enVdx(t)
To calculate the drift velocity Vdx of the electrons due to applied field E x, we first consider the
velocity Vxi of the ith electron in the x direction at time t. Suppose Velocity gained along x
Present time vx2 – ux2
its last collision was at time ti; therefore, for time (t-ti), it accelerated free of collisions, as
indicated in Figure. Let uxi be the velocity of electron i in the x direction just after the collision.
We will call this the initial velocity. Since eE x/me is the acceleration of the electron, the velocity
Vxi in the x direction at time t will be
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eEx
Vxi =u xi + t-t i
me
However, this is only for the ith electron. We need the average velocity Vdx for all such electrons
along x. We average the expression for i=1 to N electrons, as in Equation. We assumed that
immediately after a collision with a vibrating ion, the electron may move in any random
direction; that is, it can just as likely move along the negative or positive x, so that u xi averaged
over many electrons is zero. Thus,
1 eE
Vdx = Vx1 +Vx2 +......+VxN = x t-t i
N me
where t-t i is the average free time for N electrons between collisions.
Suppose that is the mean free time, or the mean time between collisions (also known as the
mean scattering time). For some electrons, (t-ti) will be greater than, and for others, it will be
shorter, as shown in figure. Averaging (t-ti) for N electrons will be the same as . Thus, we can
substitute for (t – ti) in the previous expression to obtain
eτ
Vdx = Ex
me
Equation shows that the drift velocity increases linearly with the applied field. The constant of
proportionality e/me has been given a special name and symbol. It is called the drift mobility d,
which is defined as
Vdx = dEx
Where
eτ
μd =
me
Equation relates the drift mobility of the electrons to their means scattering time . To reiterate, ,
which is also called the relaxation time, is directly related to the microscopic processes that
causes the scattering of the electrons in the metal; that is, lattice vibrations, crystal imperfections,
and impurities, to name a few.
From the expression for the drift velocity Vdx, the current density J, follows immediately by
substituting Equation, that is,
Jx = endEx
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Therefore, the current density is proportional to the electric field and the conductivity is the
term multiplying Ex, that is,
= end
It is gratifying that by treating the electron as a particle and applying classical mechanics (F=ma),
we are able to derive Ohm's law. We should note, however, that we assumed to be independent
of the field.
Drift mobility is important because it is a widely used electronic parameter in semiconductor
device physics. The drift mobility gauges how fast electrons will drift when driven by an applied
field. If the electron is not highly scattered, then the mean free time between collisions will be
long, will be large, and by Equation the drift mobility will also be large; the electrons will
therefore be highly mobile and imply high conductivity, because also depends on the
concentration of conduction electron n.
The mean time between collisions has further significance. Its reciprocal 1/ represents the
mean frequency of collisions or scattering events; that is, 1/ is the mean probability per unit
time that the electron will be scattered (see example). Therefore, during a small time interval t/.
The probability of scattering per unit time 1/ is time independent and depends only on the nature
of the electron scattering mechanism.
Mobility variation with temperature
The mobility will be made up of at least two components associated with lattice (scattering)
interactions and impurity (scattering) interactions. If the mobility is made up of several
components say 1, 2, 3, then the total mobility is given by
-1
1 1 1
μ= + +
μ1 μ 2 μ 3
If we consider just two components due to lattice scattering, L, and ionized impurity scattering,
I, then the mobility is given by
-1
1 1
μ= +
μI μL
As the lattice warms up, the lattice scattering component will increase, and the mobility will
decrease. Experimentally, it is found that the mobility decrease often follows a T -1.5 power law:
L = C1 T-1
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where C1 is a constant.
As we cool a piece of semiconductor down, the lattice scattering becomes less important, but now
the carriers are more likely to be scattering by ionized
impurities, since the carriers are moving more slowly. It is found that the ionized impurity
scattering often follows a T 1.5 power law giving:
I = C2 T3/2
Figure shows the variation in carrier mobility as a function of temperature due to the presence of
both ionized impurity and lattice scattering effects.
MATTHIESSEN'S RULE AND THE TEMPERATURE COEFFICIENT OF
RESISTIVITY ()
The theory of conduction that considers scattering from lattice vibrations only works well with
pure metals; unfortunately, it fails for metallic alloys. Their resistivities are only weakly
temperature dependent. We must therefore search for a different type of scattering mechanism.
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Consider a metal alloy that has randomly distributed impurity atoms. An electron can now be
scattered by the impurity atoms because they are not identical to the host atoms, as illustrated in
figure. The impurity atom need not be large than the host atom; it can be smaller. As long as the
impurity atom results in a local distortion of the crystal lattice, it will be effective in scattering.
One way of looking at the scattering process from an impurity is to consider the scattering cross-
section.
We now effectively have two types of mean free times between collisions; one, T, for scattering
from thermal vibrations only, and the other, 1, for scattering from impurities only. We define T
as the mean time between scattering events arising from thermal vibrations alone and 1 as the
mean time between scattering events arising from collisions with impurities alone. Both are
illustrated in figure.
In general, an electron may be scattered by both processes, so the effective mean free time
between any two scattering events will be less than the individual scattering times T and J. The
electron will therefore be scattered when it collides with either an atomic vibration or an impurity
atom. Since in unit time 1/ is the net probability of scattering, 1/T is the probability of scattering
from lattice vibrations along, and 1/1 is the probability of scattering from impurities alone, then
within the realm of elementary probability theory for independent events, we have
1 1 1
= +
τ τ T τ1
In written equation for the various probabilities, we make the reasonable assumption that, to a
greater extent, the two scattering mechanisms are essentially independent. Here, the effective
mean scattering time is clearly smaller than both T and 1. We can also interpret equation as
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follows: In unit time, the overall number of collisions (1/) is the sum of the number of collisions
with impurities alone (1/1).
The drift mobility d depends on the effective scattering time via d = e/me, so equation can
also be written in terms of the drift mobilities determined by the various scattering mechanisms.
In other words,
1 1 1
= +
μ d μ L μ1
The final result in equation simply states that the effective resistivity is the sum of two
contributions. First, T = 1/enL is the resistivity due to scattering by thermal vibrations of the
host atoms. For those near-perfect pure metal crystals, this is the dominating contribution. As
soon as we add impurities, however, there is an additional resistivity, 1=1/en1, which arises
from the scattering of the electrons from the impurities. The first terms is temperature dependent
because T T-1 but the second term is not.
The mean time 1 between scattering events involving electron collisions with impurity atoms
depends on the separation between the impurity atoms and therefore on the concentration of those
atoms (see figure). If 1 is mean separation between the impurities, then the mean free time
between collisions with impurities alone will be 1/u , which is temperature independent because
1 is determined by the impurity concentration N1(i.e., 1 =N1-1/3 ), and the mean speed u of the
electrons is nearly constant in a metal. In the absence of impurities, 1 is infinitely long, and thus
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1=0. The summation rule of resistivities from different scattering mechanism, as shown by
equation is called Matthiessen's rule.
There may also be electrons scattering from dislocation and other crystal defects, as well as from
grain boundaries. All of these scattering processes add to the resistivity of a metal, just as the
scattering process from impurities. We can therefore write the effective resistivity of a metal as
=T+R
Figure: The formation of a 2s energy band from the 2s orbital's when N Li atoms come together
to form the Li solid.
There are N 2s electrons, but 2N states in the band. The 2s band is therefore 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)
The single 2s energy level E2x therefore splits into N( 1023) finely separated energy levels,
forming an energy band, as illustrated in Figure. Consequently, there are N separate energy
levels, each of which can take two electrons with opposite spins. The N electrons fill all the levels
up to and including the level at N/2. Therefore, the band is half full. We do not mean literally that
the band is full to the half-energy point. The levels are not spreads equally over the band from EB
to ET, which means that the band cannot be full to the half-energy point. Half filled simply means
half the states in the band are filled from the bottom up.
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Figure: (a) Energy band diagram of a metal. (b) in the absence of a field, there are as many
electrons moving right as there are moving left. The motions of two electrons at each energy
cancel each other as for a and b. (c) In the presence of a field in the –x direction, the electron a
accelerates and gains energy to a' where it is scattered to an empty state near E FO but moving in
the –x direction. The average of all moment's values is along the +x direction and results in a net
electric current.
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`
Figure: (a) Energy band diagram. (b) Density of states (number of states per unit energy per unit
volume). (c) Fermi-Dirac probability function (probability of occupancy of a state). (d) The
product of g(E) and f(E) is the energy density of electrons in the CB (number of electrons per unit
energy per unit volume). The area under nE(E) versus E is the electron concentration.
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where Jx is the current density in the x-direction. Current density is defined in term of effect mass
and density as below:
nτq 2
J x = * Ex
m
where we now have a relationship between current density and electric field. This equation is in
fact just Ohm's law in a slightly different from. In order to see that equation really is just Ohm's
law we need to introduce the conductivity. The (electrical) conductivity of a material is simply
the proportionality factor between the current density and the applied electric field, which in one
dimension can be written as
Jx = xEx
where x is the electrical conductivity with units of Sm-1. The reciprocal of conductivity is called
the resistivity:
1
ρx =
σx
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write down the current density as current divided by area, and electric field as potential divided
by length to obtain
Ix V
=σ x
A Lx
Rearrange to get
Lx I x
Vx = ρ
A
Finally, use equation to obtain
Vx = IxR
which is the form of Ohm's law with which you'll be most familiar.
Drift current equations
We have now covered enough material to look at the drift current equations with some numerical
examples.
Considering intrinsic semiconductors first, in n type semiconductor electron concentration is
greater and dominating. Hence the entire conductivity is contributed by electron only
Jn = nqEn
where n = electron mobility
For holes the current density will be
Jp = pqEp
where p = hole mobility
CONDUCTION IN SEMICONDUCTORS
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Since we are dealing with intrinsic material ni = n = p and so the total current density will be
given by
J = Jn + Jp = Eniq(n+p)
giving an intrinsic conductivity of
σi = =niq μ n +μ p
J
E
For extrinsic semiconductor the current density is again due to electron and hole flow:
J = nqEn + pqEp
However, for n-type semiconductor material where n > p we obtain
n = qNdn
where Nd is the shallow donor concentration.
Similarly, for a p-type semiconductor where p>n we get
p = qNap
with Na being the shallow acceptor concentration.
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