Assignment 7 - Optical Properties Nptel
Assignment 7 - Optical Properties Nptel
Dr. S. Parasuram.
Department of Metallurgical Materials Engineering
Indian Institute of Technology, Madras
Module - 01
Assignment - 07
Optical Properties
In today’s assignment, we are going to look at the interaction of light with matter.
So, this is assignment 7, going to look at light matter interaction. So, during the course of
the lecture, we first studied how generally lights interacts with semiconductor materials,
within looked at in specific examples in applications of this. So, we looked at LED’s,
photodiodes, lasers, solar cells and so on. So, in this assignment, we will focus on the
general interaction and in the next one, we will take a problem related to the specific
devices, which a just mentioned.
So, we talked about light interacting with matter, the basic thing we said was at the
energy of the light E must be grater then some interaction energy within the
semiconductor. So, in most cases, this interaction is essentially the band gap of the
material so that, when the energy of the light is greater than the band gap, electrons are
the excited from the valence to the conduction band. We could also have situations
where there are defect states or traps states, located within the band gap. So, these could
be located either close the valence band or to the conduction band and the again the
interaction of the light the semiconductor, causes carriers to exited from either the
valence band and to the trap state or from the trap state to the conduction band. So, that
is why E semi can not only refer to the band gap of the material, but could also refer to
the energy for a defect state and a band gap. So, this brief introduction, let me go the
problems, as we go through the problems we will again related to the concepts that we
delta within the lectures.
Problem 1. So, we have a sample of gallium arsenide which is 0.35 micro meters thick, it
is illuminated with the light source and the energy is given. So, energy E is 2 electron
volts. This is greater than the band gap of gallium arsenide, so E g of gallium arsenide,
which is 1.42 electron volts. Determine the percentage of light, absorb through the
sample and we want to repeat the calculation for silicon. So, when we look at light of the
absorption through a material, we basically go back to the Beer Lambert law.
The Beer Lambert law's says that, the change in intensity over a small distance d x and
there is negative sign because, the intensity actually goes down, is directly proportional
to x and the proportionality constant is call mu. mu here is the absorption coefficient of
the material. This intern depends upon the wavelength of the light that is shining through
this. We can integrate this and basically put the boundary conditions, which gives us I is
equal to I not exponential minus mu x. So, I here represent the transmitter intensity. So,
if we want find the absorb intensity and if you want to find it as the ration, it is nothing,
but 1 minus I over I not.
So, this is essentially a ratio, which we can convert to a percentage so which is 1 minus
exponential minus mu. In this particular case, we have been given the thickness of the
sample. So, t here refers to the thickness. So, we can basically use this expression to
calculate the value for gallium arsenide.
So, for gallium arsenide, the absorption coefficient mu is given. So, mu is 5 times 10 to
the 5 per centimeter inverse. So, from this, we can calculate the percentage absorb which
is just 1 minus I over I not times 100 and here we substitute all the values this works out
to be 99.999 and there are few more trailing 9s which means, when you shine the light of
2 electron volts on a sample of gallium arsenide, there is only 0.35 micro meters thick.
So, 0.35 is just; 350 nanometer. So, it is only 350 nanometers and almost; all the light
absorbed so that, gallium arsenide is essentially opaque to this radiation.
We can do the same calculation for silicon the value of mu its 8 time 10 to the 4 per
centimeter. So, silicon actually has lower band gap then gallium, gallium arsenide. So, E
g of silicon is 1.10 electron volts at room temperature. So, even though it has lower E g,
the value of the absorption coefficient a 2 electron volts is slightly lower than that of
gallium arsenide and this basically related to how the density of the states is distributed
in the valence and the conduction band. So, taking this value of mu, we can calculate the
percent absorbed; can again plug in the numbers. This is 93.92percent. So, it is still a
high number, but nearly 7 percent of the light gets through, well the reset is the absorbed.
So, we can actually go beyond and do some more calculations just to get a feel of this
value. So, instead of 0.35 micrometers, I know reduce my thickness to 0.1 micro meters.
This is approximately 100 nanometers. My energy is still 2 electron volts so that, I can
use the same values for the absorption coefficient. If you do that for gallium arsenide, the
percent absorb is 1 times 100, this is 1 minus exponential minus mu t times 100 and this
is ninety 99.3. So, when we reduce the thickness further, so we actually take it down,
were on 3 times, you go from 350 nanometers to 100 nanometers, still we get a really
high percentage of light that is absorbed.
So, for silicon on the other hand, the percent absorbed for 100 nanometers is only 55
percent. So, only the half the light absorbed and the other half gets transmitter and other
variable we can introduce, is to change the wave length of the energy of the light.
So, if you take energy to be 1.5 electron volts. So, instead of shining light of 2 electron
volts, we shine light of only 1.5 electron volts. For gallium arsenide mu is lower, so its 5
times 10 to the 3 for centimeter, 5 time 10 to the 3 per centimeter. So, this is still above
the band gap, but it is very close to the band gap so that, the numbers of available states
are small. So, correspondingly the absorption coefficient is also small.
Now if you have a thickness of 0.35 micro meters, so the same 350 nanometers, the
percentage absorbed fusing the same formula is only 16.05. So, nearly 84 percent of the
light is transmitter, while the rest is absorbed. So, the absorption coefficient mu place a
really key role in determining the thickness of the sample that you need, in order to either
get light to get completely pass through or light to be absorbed. So, if we are trying to
build a transparent semiconductor with gallium arsenide, we find that if you have light of
energy greater than 1.5 electron volts and this is already in the visible region, we find
that most of the light essentially gets absorbed and only a small percentage of light get
transmitted.
So, the value of mu and the corresponding at different wavelengths, something the place
of very important role in determining the type of material you choose and also thickness
of the material. So, let us now go to problem 2.
If, the x is minority lifetime is 10 micro seconds. So, the minority lifetime this 10 micro
seconds. We are also calculate the study state excess carrier concentration. So, we look at
the first part of the problem. So, we have light of wavelength 630 nanometers. So, the
first thing is to calculate the energy. Energy is nothing, but h c over lambda, in this
works out to be 3.16 times 10 to the minus 19 joules. So, we also know the intensity of
the light. So, I is 1 watt which is 1 joule per second. So, we can calculate the total
number of photons. So, this is the numbers of photons that add incident per second. This
is equal to I divided by the energy. So, I divided by head see over lambda. So, we can
plug in the numbers this works out to be 3.17 times 10 to the 18 photons per second.
So, we also want to calculate the electron hole pairs for unit volume. So, volume is
nothing but A times t, so, 0.1 centimeter q. So this, we can divide by the volume, we also
say that each photon gives rise to 1 electron hole pair. So, this means, there is quantum
efficiency of 100 percent, usually that is not the case, the efficiency would be lower than
hundred in which case you will have to multiply by the appropriate fraction. But for this
particular problem, we will take the quantum efficiency to be 100 percent. So, this is a
number of photons that are incident, these will give rise to an equal number of electron
hole pairs.
So, the number of electron hole pairs per unit volume is nothing but, 3.17 times 10s to
the 19 per centimeter cube per seconds. We just are dividing the number of photons by
the volume. So, in the next part, we are asked to calculate study state excess carrier
concentration. So, we do not know this material is a p type or an n type semiconductor.
So, just for simplicity, I will take it to be an n type so that, the excess carriers or holes.
We can do this same thing by assuming material to be a p type so that, the excess
minority carriers are electrons, but it will not affect the final result.
So, these are the excess minority carriers. So, when we have light illuminating on a
sample, it is possible to write an equation for the excess carriers. This differential
equation just as d delta p over d t, so it delta p represents the excess minority carriers
there are created this is equal to the number of electron whole piers that are generated,
minus delta p n over h were h is the minority lifetime. So, when we basically have study
state, delta p is 0. So d delta p over dt 0 at study state, which implies; the study state
excess carrier concentration is nothing, but the number of electron hole pairs that as
generated, times lifetime of the minority carriers.
So, this we can again substitute, we know the lifetime is given to be 10 micro seconds;
the number of carriers per unit volume is something which is calculated.
(Refer Slide Time: 19:46)
So, this is equal 3.17 times 10 to the 14 per centimeter q. So, these are the excess holes at
study state. So, let us now go to problem 3.
So, problem 3, we have a direct band gap semiconductor with no trap states. So, we do
not have any defects or traps that are located within the band gap. So, this is important
because, traps state can usually trap the carriers and these have longer lifetime then the
electrons and the holes in the band. This will again change the carrier lifetime and that
will again affect properties like the conductivity and also the quantum efficiency. So, we
have a direct band gap semiconductor. It is illuminated with light of intensity, so I of
lambda. So, in this case I is a essentially of the function of the wavelength. This causes
photo generation.
So, once again we are saying that the wavelength lambda or the energy of the light is
greater than the band gap so that, we have electron hole pairs that are created. The area
of the illumination is given. So, A is length times W and the thickness of the
semiconductor is d. If the eta is the quantum efficiency, quantum efficiency defines how
many electron hole pairs are, how many photons are converted to electron hole pairs. In
the last problem, we assume the quantum efficiency p to be 1 so that, every photon gets
converted to a electron hole pair. It take the quantum efficiency to be 0.5 or 50 percent, if
we have 2 photons coming in, only 1 of them will get converted to an electron hole pair.
The quantum efficiency is given and is the re combination of lifetime of the carriers. So,
when we shine light in a material, we generate excess electrons in holes. These electrons
in holes can basically take part in conduction so that, there is a change in conductivity
when we expose light. This is essentially call photo conductivity and that difference in
conductivity delta sigma is defined as sigma in the presence of light, minus sigma in the
absence of light typically that is a dark state. And we have to show that, delta sigma is
equal to e eta I lambda mu e plus mu h over h c d.
So, in some ways problem 3 is similar to problem 2, except that we are using symbols
instead of numbers and in the last part of problem 3, we will actually plug in some
numbers to get this expression. So, once gain first thing we need to do is to calculate the
number of photons or the photon fluxes that is incidents on the samples. So, 5 ph is
photon flux, this is given by I is the intensity divided by h c over by lambda, which is the
energy. So, this is the intensity and then this is the energy. So, this is I lambda over h c.
So, we define quantum efficiency, as the number of the electron whole pairs that are
generated for a certain photon flux. So, it G ph which is the number of electron whole
pairs generated nothing, but eta which is the quantum efficiency times gamma p h, so
this I lambda eta over h c. So, in this particular problem, the intensity is given per
second. So, intensity is given per unit area. So, it calculate volume change or to calculate
the number of electron hole pairs there are generated for unit volume, we basically need
to multiply by the area and also divide by the volume.
So, the number of electron hole pairs per second per unit volume. So, again I am going to
use the same symbol G p h, but now this for unit volume is nothing, but eta cans gamma
p h times A divide by the volumes. So, A can get cancelled, we can plug in the value of
gamma p h. So, this is nothing, but eta I lambda over h c d. So, again we have a steady
state situation. So, we can write the continuity equation.
So, if we take the excess carriers to be electrons, then b delta n over d t is nothing, but G
p h minus delta n over. And at steady state, this change is equal to 0. So, delta n is G p h
times, we can substitute that expression. So, it is tau eta I lambda over h c D. So, this is
the excess electrons there are generated, this must be the same as the extra holes because,
electron hole pairs are generated. So, every time in electron is generated holes is also
generated.
So, the change in conductivity delta sigma is nothing, but delta n e mu e plus delta p e
mu h. These 2 terms are the same an equal to this. So, this you could take it out and when
you re write, you get the final expression delta sigma is e eta I lambda u e has mu h
divided by h c D. So, in some ways is very similar to the previous problem, excepted that
instead of putting numbers, we have divide a more general expression that takes into
account, the lifetime of the carriers and also the excess carriers there are generated.
So, now, we try to put some numerical values to this. So, now we say that, the material
we have cadmium supplied.
So, problem.
(Refer Slide Time: 32:43)
So, problem 4, we have gallium arsenide sample is illuminated with the helium neon
laser b. So, you have a helium neon laser. The wavelength of laser light is 632.8
nanometers and the intensity is 50 mill watts. We want to calculate how much power is
dissipated as heat in the sample due to thermalisation. So, once again, we can calculate
the energy. Energy E equal to head c over lambda is 1.96 electron volts. So, this is
greater than E g of gallium arsenide which is 1.42 electron volts.
So, what happens is that, the excess energy of the photons basically gets translated in to
excess energy of the electrons in holes. This excess energy is lost has heat to the
surrounding material and this is essentially a thermalisation process. So, it calculate the
energy lost of the power lost thermalisation, we worst need to calculate the number of
photons this is again I over h c over lambda, which gives you the number of photons. So,
excess energy which is the electrons and holes posses are essentially lost to the lattice
and when the energy is lost, the electrons come close to the conduction band edge or the
hole goes close to the valence band edge. Here is a always a certain thermal energy
which the electron will posses.
So, the final energy of the electron after thermalisation is nothing, but E g which is the
band gap plus 3 over 2 k T this is with respect to the top of the valence band so that, the
top of the valence band is taken as 0. So the energy of electron, after losing the excess
energy to the lattice is just E g plus 3 half k T. So, this is the initial energy of the electron
this is the final energy. So, the total energy lost delta E is nothing, but h c over lambda
minus E g plus 3 halves k T. This energy lost we do the numbers is 0.503 electron volts.
So, this energy is lost by electron that is generated, which is equal to the total number
photons that are incident.
So, that the total power that is lost is nothing, but gamma p h times delta E which
nothing, but the incident power p l divided by h c over lambda times delta E. So, this is
nothing, but the ration of the incident power to the final energy of the energy that is lost,
which depends upon the band gap. So, all these values are known; p l is 50 milli watts.
So, if you substitute this works out to be 12.76 mili watt lost to thermalisation.
If you increase the energy of the incident right, so instead helium neon with 1.96
electrons volts, we have a higher energy light. The value of delta E will be higher, which
means more amount of power will be essentially lost to thermalisation. So, this is
important, when we decide what kind of incident radiation we want in order to
generative electron hole pairs. So, if there is large mismatch between the incident energy
and the band gap of the material, most of the heat will essentially will be lost
thermalisation. If we trying to operate this in the form of device, this heat lost in
basically increase the temperature of the device and cause the device to be more
inefficient.
So, before shining light, we can basically calculate the position of firmy level. So, we
can calculate position of E F before shining light. So, this is nothing, but an n type
semiconductor. So, that E f N minus E F I is k T lon of N D over n i. This works out to
be 0.298 electron volts and this will be above p f I. So, we now shine light and the light
generates excess electrons and holes. So, you new electron concentration n is nothing,
but N D plus delta n which works out to be 1.1 times 10 to the 15 per centimeter cube.
So, we have excess concentration of electrons, is will again cause a slight shift the firmy
level. This your quazi firmy level. So, the new E F N minus E f I is k T lon n over n i
were the value of n is now 1.1. So, this gives you 0.3004. The shift is very small because,
increase is not that much, but there is still a small shift in the firmy level.
(Refer Slide Time: 42:20)
We can also do a similar calculation for the holes E F P minus E F I is minus k T lon of P
over n i at P is delta P which excess carrier then there are generated. This is equal 10 to
the 14 per centimeter cube. So, if you do this E F P minus E F I is minus 0.238 electron
volts, this is basically below E F I. So, when we shine light on to the material, we
generate excess electrons in the holes, we can define a quazi firmy level for this excess
electrons and holes and we just take the calculation, taking the n separately and the
taking the p separately. These in not reflect the real firmy level in the material because,
these are excess that are generated during elimination, when we can treat them as n an p
type semiconductors, in get an idea of where the firmy level will be located.
We now want to calculate the excess conductivity delta sigma. So, you find that, there is
only a small increase in the electron concentration, but there is a drastic increase in the
hole concentration. For the change in conductivity, we do more all as driven by this
excess hole concentration. So, delta sigma is nothing, but delta P E mu h. So, we ignore
the change in minority carriers an only look. So, ignore the change in the majority
carriers an only look in the minority carriers. So, mu h is not known, but we do know the
value of D P, D P is 12 centimeter square per second and this is nothing, but k T mu h
over E.
So, from this we can calculate the value for mu h, mu h works out to be 463.8 centimeter
square per volt per second. So, this we can substitute here and you can calculate the
change in conductivity and this is driven by the excess holes 7.42 times 10 to the minus 3
on inverse centimeter. So, we can treat a semiconductor, which has non equilibrium
concentration of electrons and holes has essentially and n and the p type separately. And
then, we can basically calculate the increase in conductivity and this in increase in
conductivity is mainly; due to the increase in the minority carrier concentration.