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Language: en

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Hello everyone, welcome to lecture 34
of the online course on Nanophotonics,

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Plasmonics and Metamaterials. Today's
lecture will be on Nanofabrication. So,

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in this lecture we will see the most mostly used
nanofabrication methods and we will discuss about

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thin films and different ways of making thin
films like physical methods, chemical methods and

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epitaxy and then we will conclude this lecture.
So, this particular module will give you a brief

00:01:04.280 --> 00:01:11.680
overview of how different fabrication methods
can help you realize the structures that we have

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studied in this particular course. So, it will
not be a very extensive overview or in detail

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study of the different fabrication methods. I will
try to catch and touch upon different topics so

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that you have basic idea of how to realize
the structures that we have discussed.

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So, when we talk about nanofabrication,
nanofabrication lacks a clear definition

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and it is not very distinctly separated
from the term microfabrication. So,

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new methods are constantly developed to
make electronic components smaller starting

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from micrometers to nanometers and the same
techniques can also be used for nanophotonics,

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plasmonics and metamaterials. So, microfabrication
that those are typically done for larger parts

00:02:07.120 --> 00:02:14.560
will become nanofabrication when the parts shrink
and the dimensions become almost comparable to

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nanometers ok. So, the basics remain similar.
Now, integrated circuit production drives this

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particular technology and they provide extra
advantages in the areas like photonics. Tools

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and techniques keep evolving with time there
is a constant research and updation going on to

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make the process more robust so that there are
less fabrication error and the yield increases

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and there are also challenges coming from
continuous shrinking of the component sizes. So,

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the process has resulted in smaller and smaller
electronic parts with widespread benefits that

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is why you see all these devices they are becoming
very lightweight and small compact these days. So,

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that is because of the advancement in
nanotechnology that allows the scientists

00:03:14.720 --> 00:03:20.760
and engineers to fabricate structures
which are really really small. Now,

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if you look into nanofabrication there are mainly
three parts thin films lithography and etching.

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So, thin films as you can see there will be a
substrate and you can develop a thin film on top

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of that this film thickness can be typically few
to several nanometers ok or even micrometers ok

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those are thin films. Then you have lithography
lithography is basically a process of making

00:03:48.680 --> 00:03:57.400
patterns ok. So, you can see it starts with a
silicon substrate which is coated with a photo

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or e-beam resist. We will come into the details
of this in the next lecture, but let us quickly

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go through what it looks like. Then you will
basically have a hard or soft mask which actually

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got the pattern that you want to develop and then
when you expose UV or electron beam ok your your

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photoresist ok if they are positive photoresist
they get developed ok and then they can be etched

00:04:27.320 --> 00:04:35.440
away by some kind of solvent and this is the
pattern of the resist that remains ok.

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So, after that you can evaporate material and that
material fills in this particular gap and then

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when you remove this photoresist completely
these are the patterns which are basically

00:04:48.800 --> 00:04:57.480
developed on the silicon. So, you can this is
done by putting this in a lift of solvent. So,

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all these are the standard processes in
nanofabrication technology. So, we will look

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into this in the next lecture. Today we will be
mainly covering thin films and in the last lecture

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of this module we will be covering etching ok.
So, here you can see that you have got a circuit

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material that needs to be etched and you develop
a photoresist first on that ok and then you can

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expose these areas of the circuit material
to the etch they can etch away those circuit

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material and this is what you get after
etching. So, these are the 3 methods that

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actually help you develop those structures that
you have seen in this particular course ok. So,

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these as you can see these methods are very much
standardized and optimized for semiconductor

00:05:51.880 --> 00:05:59.520
industry and that is where people are actually
aiming towards making photonics material CMOS

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compatible. So, that the same foundry with some
minor modification can help us fabricate those

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nanophotonic structures or plasmonic structures.
If we are going for totally different materials

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that might be difficult for mass production
at this current stage when the foundry is not

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supporting those kind of material fabrication.
So, if you look into the thin film industry,

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thin film size science is basically a broad
field which is used in various industries ok

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and thin films are ultra thin layers that can be
found in products such as eyeglasses ok screens

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and vehicles and these are different kind of
purposes something like reducing reflection

00:06:52.920 --> 00:07:00.280
preventing damage and altering properties. In
tiny computer parts these thin films can control

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electricity and help you switch ok. So, another
important application you can think of is the

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gate direct link in transistors which is often
less than 10 nanometer thick. So, those are also

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thin films. So, here you can see applications of
thin film in different different disciplines.

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So, if you think of optics it can give you
anti reflection coating, highly reflected

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coating something like laser mirrors you can
have interference filters beam splitter then

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thin film polarizers integrated optics and so
on. If you think of optoelectronics you can

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use them for photo detectors image transmission
optical memories LCD TFTs and all this. If you

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think of electronics they can be like passive
thin film elements like resistors condensers

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and interconnects you can think of active thin
film elements like transistors and diodes ok and

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integrated circuits like VLSI circuits they also
use a lot of thin films. Then CCD charge coupled

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device you can think of chemistry where catalysis
electro catalysis biocatalysis photo catalysis

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all those things are the application you can think
of sensors you can think of magnetic applications

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engineering and processing and also new materials
I will not read out all of them, but you can

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always see that there are lot of applications
of thin films. They are also very useful in

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biomedicine where you can have neurological
sensors you can have claddings for a depot

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pharmacy and biocompatible implant coatings.
So, all these things are possible. So,

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there are vast application of thin film technology
not only in the area of semiconductor or photonics

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they can actually have applications in lot more
other disciplines ok. They can be used for

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alternative energy or green energy something like
in solar collectors or solar cells and so on ok.

00:09:13.800 --> 00:09:21.280
So, as I mentioned earlier this thin films can
be really really thin and they can be from 10

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to 1000 nanometers. So, typically 10 nanometer
to 1 micron that is what we call them as thin

00:09:28.240 --> 00:09:37.480
films ok and these are for visible and infrared
light and for extreme UV light the films will

00:09:37.480 --> 00:09:43.960
become even more thinner because extreme UV
light has got a very short wavelength and in

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that case you can actually use thin films of 1
to 2 nanometer thickness and these are typically

00:09:50.360 --> 00:09:57.200
used in photo masks will come into this.
So, right now just keep this new terms in mind

00:09:57.200 --> 00:10:04.360
we will discuss about this new terms soon in this
lecture or in the subsequent lectures. Now, thin

00:10:04.360 --> 00:10:12.960
film properties change based on how they are made.
So, the key properties include how well they coat

00:10:12.960 --> 00:10:20.920
the surfaces, their density and their electrical
behavior and density affects how light bands in

00:10:20.920 --> 00:10:29.160
the film and stress can wrap or crack it. So, this
is the effect of density when the thin films are

00:10:29.160 --> 00:10:36.280
made from compounds the films make up can vary
depending on how it is created and for single

00:10:36.280 --> 00:10:42.960
element thin films it is not usually of a worry
and when you develop thin films the impurities

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grain size and how tightly the elements of the
particles are packed they also affect how well

00:10:49.720 --> 00:10:57.800
the thin film will conduct electricity. So, their
conductivity depends on all these parameters.

00:10:57.800 --> 00:11:04.640
Now, how do you make thin films? So, the process
of making thin films can be broadly classified

00:11:04.640 --> 00:11:12.920
into 2 categories physical methods and chemical
methods. Physical methods involve transferring the

00:11:12.920 --> 00:11:20.400
material from the source to the substrate without
changing its chemical state. So, it is a physical

00:11:20.400 --> 00:11:27.240
method. On the other hand when you think of
chemical method it the film is basically created

00:11:27.240 --> 00:11:34.840
as a byproduct of some chemical reaction. So,
let us look into the physical methods first.

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So, when you talk about physical methods there
are 2 widely used methods for adding thin films

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one is evaporation another is sputtering. So, this
methods work like a special kind of painting with

00:11:50.120 --> 00:11:57.200
the vaporized material adding tiny particles
to a particular substrate that will be the

00:11:57.200 --> 00:12:03.240
surface that you will be coating with the thin
material. Evaporation or sputtering are part

00:12:03.240 --> 00:12:10.800
of a group called physical vapor deposition
or PVD. In PVD the materials are transformed

00:12:10.800 --> 00:12:18.560
into vapor and then layered onto a surface one
atom at a time and these processes are often

00:12:18.560 --> 00:12:28.360
carried out in high vacuum chambers that prevent
interference from gases in the surrounding. So,

00:12:28.360 --> 00:12:34.400
if we look into the evaporation method
evaporation method involves heating

00:12:34.400 --> 00:12:41.480
the source material a lot until it turns into
vapor and vapor pressure plays a very important

00:12:41.480 --> 00:12:48.120
role here because all materials evaporate at
specific temperatures as you can see here.

00:12:48.120 --> 00:12:55.680
So, this is basically the pressure it is
given in millibar this one is in torr and

00:12:55.680 --> 00:13:02.560
this is the temperature scale ok. So, that is
in centigrade and that is in Kelvin ok. So,

00:13:02.560 --> 00:13:08.600
and here are the materials like tungsten,
gold, magnesium there are many more all

00:13:08.600 --> 00:13:14.680
listed here ok. So, this is basically a vapor
pressure versus temperature curve for different

00:13:14.680 --> 00:13:21.760
kind of metals. So, commonly used materials
barely evaporate at room temperature right.

00:13:21.760 --> 00:13:31.040
So, you can see that gold with a very low vapor
pressure below 10 to the power minus 15 torr at

00:13:31.040 --> 00:13:40.480
room temperature ok. Now, when you see how
the vapor pressure for gold is changing ok

00:13:40.480 --> 00:13:47.720
with temperature. So, you can see that at
1500 degree centigrade it actually changes

00:13:47.720 --> 00:13:56.560
to 100 milli torr ok. And the vapor pressure also
depends on the position in the vapor stream. So,

00:13:56.560 --> 00:14:02.720
the pressure decreases as the vapor moves
away from the source, make sense.

00:14:02.720 --> 00:14:10.480
So, the closest it is to the source it will be the
highest vapor pressure. So, vapor pressure on the

00:14:10.480 --> 00:14:17.920
surface where the film forms can be estimated
from the vapor flow patterns. And to calculate

00:14:17.920 --> 00:14:24.080
the film growth rate pressure connects to
the rate of atoms hitting the surface. So,

00:14:24.080 --> 00:14:31.000
that way you can calculate the rate at which
your thin film will be growing. Often instead

00:14:31.000 --> 00:14:36.160
of directly measuring the temperature and
vapor pressure deposition rate is controlled

00:14:36.160 --> 00:14:43.000
by adjusting the power to the source.
So, that is also another method to adjust

00:14:43.000 --> 00:14:52.880
how much the temperature how much thickness
will be deposited. So, among the two methods of

00:14:52.880 --> 00:15:00.880
evaporation you can see here one method is called
resistively heating evaporation process. So,

00:15:00.880 --> 00:15:05.580
in this particular process there are two
methods. So, this is the one the other one

00:15:05.580 --> 00:15:11.560
will show in the next slide. So, in this one
the palette of the source material that is here

00:15:11.560 --> 00:15:17.200
it is actually put in a metal container
like a boat ok and it is heated using a

00:15:17.200 --> 00:15:24.200
strong electric current around 100 amperes.
So, this is particularly called resistively

00:15:24.200 --> 00:15:32.960
heated evaporation. So, it is very simple
needing only a low voltage DC source,

00:15:32.960 --> 00:15:39.680
but it has got some drawbacks. Drawback something
like it is inefficient and there are chances of

00:15:39.680 --> 00:15:45.880
potential contamination due to other parts
also getting heated up and evaporating along

00:15:45.880 --> 00:15:51.840
with the source. So, this boat material or
other parts also may get heated up and they

00:15:51.840 --> 00:15:56.480
they will also vaporize along with the source
material. So, this is how it works the source

00:15:56.480 --> 00:16:04.160
material or evaporation material is here the
filament or the heater element is here.

00:16:04.160 --> 00:16:11.360
So, it hits this one up the vaporized material
particles they actually go and settle down on

00:16:11.360 --> 00:16:17.720
the substrate which is kept right on top of
it and this is done in a vacuum chamber. The

00:16:17.720 --> 00:16:23.160
second method is called a electron beam
heating ok where the heated electrons are

00:16:23.160 --> 00:16:30.680
basically accelerated by high voltage. So, here
you see the amount of voltage requirement goes

00:16:30.680 --> 00:16:36.520
very very high it is around 10 kilovolt and
then it is focused this particular electron

00:16:36.520 --> 00:16:43.160
beam is focused on to the source palette.
So, this happens again inside a vacuum. So,

00:16:43.160 --> 00:16:51.560
the electrons can be controlled by magnetic field
ok and without heating the gas molecules.

00:16:51.560 --> 00:16:58.040
This particular method of electron beam
evaporation is pretty efficient and here

00:16:58.040 --> 00:17:04.320
accurately heating of the source can be obtained.
So, that it minimizes the contamination and

00:17:04.320 --> 00:17:11.560
therefore, it is a good process of developing in a
high quality thin films, but only problem is that

00:17:11.560 --> 00:17:19.840
it requires a complex high voltage power source.
And safety also becomes important here because you

00:17:19.840 --> 00:17:26.400
are dealing with very high voltage. Now, despite
this electron beam evaporation is widely used in

00:17:26.400 --> 00:17:33.640
thin film research and development the reason you
get a very high quality film. Now, the next method

00:17:33.640 --> 00:17:41.120
of developing thin film is called sputtering.
So, sputtering also uses a vacuum system with

00:17:41.120 --> 00:17:48.960
an excited gas plasma ok. So, this is
the typical setup for sputtering. So,

00:17:48.960 --> 00:17:58.800
here you can see that there is a gas inlet this
is the outlet and the sputtering gas comes in

00:17:58.800 --> 00:18:08.080
and it hits the cathode sputtering target ok.
So, that knocks out the metallic particles or

00:18:08.080 --> 00:18:15.280
atoms and they actually go and settle down
on the substrate forming a thin film ok.

00:18:15.280 --> 00:18:22.800
So, here you can see how it works. So, plasma ions
so these are the plasma ions which are so this

00:18:22.800 --> 00:18:29.800
is plasma and then the sputtering gas enters
and the plasma ions are basically directed at

00:18:29.800 --> 00:18:37.040
the cathode and they could knock the neutral
atoms of the surfaces. You can see here M is

00:18:37.040 --> 00:18:45.160
the metal that is been knocked off ok and these
atoms they collect on all surfaces including

00:18:45.160 --> 00:18:53.440
the substrate. So, you can see a thin film being
growing on this it is because of this ok. Now,

00:18:53.440 --> 00:19:01.320
in this particular method unlike evaporation
it does not depend on heating ok. So,

00:19:01.320 --> 00:19:08.960
what is the method of atoms coming out? The
the atoms are basically ejected by momentum.

00:19:08.960 --> 00:19:17.800
So, this leads into much denser films ok. However,
there are some benefits with sputtering because it

00:19:17.800 --> 00:19:24.400
is more flexible and that is why it is popular in
the industries compared to evaporation. Heating

00:19:24.400 --> 00:19:29.280
is not required high voltage requirement is
not there. So, it is pretty good. Targets

00:19:29.280 --> 00:19:37.080
and plasma sources in sputtering can be made
of different shapes for various coating

00:19:37.080 --> 00:19:43.720
setups something like circles rectangles or
any other unusual shape you can coat ok.

00:19:43.720 --> 00:19:52.320
Sputtering can happen upward downward or sideways
while evaporation happens only upward ok. So,

00:19:52.320 --> 00:19:57.880
these are the flexibilities with the sputtering
technique. Moreover, the plasma power in the

00:19:58.400 --> 00:20:08.000
sputtering comes from a DC or RF source ok. So,
for metal targets DC sputtering works whereas,

00:20:08.000 --> 00:20:16.600
for insulating targets RF sputtering is used where
the target acts as the capacitor for the plasma.

00:20:16.600 --> 00:20:20.880
We will not go into too much of detail, but it
is good to know what are the different techniques

00:20:20.880 --> 00:20:28.560
being used for developing what kind of films.
So, RF excitation needs a matching network due

00:20:28.560 --> 00:20:37.680
to variable impedance and it is used for both
conductive and non-conductive targets ok. In

00:20:37.680 --> 00:20:46.440
sputtering the atoms collide before reaching
the substrate due to plasma gas making it less

00:20:46.440 --> 00:20:55.360
directional than evaporation. So, these are couple
of pros and cons of sputtering as compared to

00:20:55.360 --> 00:21:01.440
evaporation. There is a variation to it which
is called reactive sputtering and in reactive

00:21:01.440 --> 00:21:10.240
sputtering what happens a bit of reactive gas
like oxygen or nitrogen mixes with the argon gas

00:21:10.240 --> 00:21:19.960
to create compounds from ejected target molecule
ok. So, the setup looks like this you have got a

00:21:19.960 --> 00:21:24.920
power supply here this is the target which is
kept this is the plasma formation you have got

00:21:24.920 --> 00:21:30.520
argon gas and also you get some reactive
gas and this is the vacuum chamber ok.

00:21:30.520 --> 00:21:40.000
And from the target these are knocked off and
then the materials or nanoparticles which are

00:21:40.000 --> 00:21:49.440
ejected from this target gets reacted with this
reacting gas and then the compound gets deposited

00:21:49.440 --> 00:21:54.600
on the substrate. So, during this process
as you can see the atoms are ejected from

00:21:54.600 --> 00:22:03.240
the target by energized ions to form a plasma
that is directed to the substrate under a high

00:22:03.240 --> 00:22:12.280
vacuum. Argon is commonly used as the sputtering
gas and the sputtering is carry out with DC

00:22:12.280 --> 00:22:19.280
power source and RF alternating current or ion
assisted deposition there are 3 methods. So,

00:22:19.280 --> 00:22:26.280
mainly DC and RF sputtering are used and in
this particular case of reactive sputtering

00:22:26.280 --> 00:22:33.360
a reactive gas such as oxygen are used for
getting oxides. You can use nitrogen if you

00:22:33.360 --> 00:22:39.280
want to create thin films of nitrides ok.
They are also passed to the reaction chamber

00:22:39.280 --> 00:22:45.880
along with the argon gas that you can see here and
this reactive gases react with the target atoms

00:22:45.880 --> 00:22:53.000
in the plasma to form the desired composition and
then they get deposited in the film as I explained

00:22:53.000 --> 00:23:00.360
before. So, while forming perovskite oxide films
multiple targets with different elements are

00:23:00.360 --> 00:23:10.320
simultaneously sputtered which are reacted with
oxygen and they deposit as the desired film. Since

00:23:10.320 --> 00:23:17.240
the target elements and oxygen exhibit a large
electronegativity difference the formed ions can

00:23:17.240 --> 00:23:22.920
be negatively charged and they can be accelerated
towards the substrate due to the difference in the

00:23:22.920 --> 00:23:31.120
potential of the negatively charged target and
the grounded substrate ok. So, the substrate is

00:23:31.120 --> 00:23:40.440
grounded ok. This ionic fluxes possibly act as
sputtering ions to re sputter the growing thin

00:23:40.440 --> 00:23:48.560
films onto the substrate or modify the composition
of the films or etching the substrate ok.

00:23:48.560 --> 00:23:58.200
So, the next method to develop thin film is pulsed
laser deposition. So, here the name itself tells

00:23:58.200 --> 00:24:06.520
you that you are going to use a laser pulse ok
for depositing thin films. So, how it works? So,

00:24:06.520 --> 00:24:15.040
pulsed laser deposition or PLD employs brief
powerful laser pulses which are as short as few

00:24:15.040 --> 00:24:20.360
nanoseconds to remove the target material. So,
you can see in the diagram here you have got a

00:24:20.360 --> 00:24:26.760
laser pulse you focus it and you hit the target
ok. And then there is a plasma plume that goes

00:24:26.760 --> 00:24:33.120
towards the substrate and it gets deposited.
So, the laser energy here is focused on the target

00:24:33.120 --> 00:24:42.360
subs surface causing rapid material evaporation
and atom injection. So, that gives you this

00:24:42.360 --> 00:24:51.800
plasma plume ok and the atoms then they gather
on the surface to give you that thin film. So,

00:24:51.800 --> 00:24:58.960
what is the key advantage of this PLD? It can be
performed in ultra high vacuum or with various

00:24:58.960 --> 00:25:08.960
pressures and gases due to the laser source being
external to the vacuum chamber. So, that that is

00:25:08.960 --> 00:25:16.880
the flexibility it provides and the main advantage
of PLD is its ability to remove target materials

00:25:16.880 --> 00:25:25.320
in stoichiometric manner that treating all atoms
equally due to high laser fluency and rapid

00:25:25.320 --> 00:25:33.400
ablation. So, that way you are able to deposit
uniform films using pulsed laser deposition.

00:25:33.400 --> 00:25:40.160
So, PLD is particularly suited for complex
ceramic films like yttrium barium copper

00:25:40.160 --> 00:25:50.680
oxide YBCO lead zirconate titanate PZT and
different other carbides oxides nitrides ok that

00:25:50.680 --> 00:25:57.240
are challenging to deposit using other methods.
So, you can actually deposit this kind of films

00:25:57.240 --> 00:26:05.320
using PLD method. So, as I told you that the main
advantage of PLD is that it is non discriminatory

00:26:05.320 --> 00:26:15.280
and it gives you stoichiometric removal of
target atoms ok and it facilitates and it comes

00:26:15.280 --> 00:26:22.200
from rapid ablation and high laser fluency. So,
quickly this evaporation takes place and it takes

00:26:22.200 --> 00:26:29.280
place from all from the entire target.
So, that happens very very quickly. So,

00:26:29.280 --> 00:26:36.240
with that we more or less cover all the basic
methods in this particular physical methods of

00:26:36.240 --> 00:26:45.080
depositing thin films. Now, let us look into the
chemical methods of depositing thin films. As we

00:26:45.080 --> 00:26:51.120
mentioned before that chemical methods will
deposit the thin films as a byproduct of some

00:26:51.120 --> 00:26:57.960
chemical reaction. So, chemical methods they
offer uniform well covered and stoichiometric

00:26:57.960 --> 00:27:05.280
films, but different gases and chambers are
often required for each type of film.

00:27:05.280 --> 00:27:12.600
So, that makes it very very specific. So, so
and it is that makes it also costly if you are

00:27:12.600 --> 00:27:18.640
experimenting in different films because and
using different gases. So, you need different

00:27:18.640 --> 00:27:25.280
different chambers for different film types.
So, the most common chemical method is chemical

00:27:25.280 --> 00:27:32.200
vapor deposition where gas precursors enter
a chamber and the high substrate temperature

00:27:32.200 --> 00:27:40.920
prompts a reaction to build the desired film. So,
different types of CVDs are there one is called

00:27:40.920 --> 00:27:48.280
low pressure CVD, you have atmospheric pressure
CVD, you have plasma enhanced CVD and atomic layer

00:27:48.280 --> 00:27:55.760
deposition. So, CVD requires low pressure and
high substrate temperature that ensures that the

00:27:55.760 --> 00:28:03.840
reaction occurs only on the substrates surface
and not in the gas phase which could lead to

00:28:03.840 --> 00:28:12.840
particle formation and surface deposition.
So, here is the setup typically used for low

00:28:12.840 --> 00:28:20.560
pressure CVD. So, in this particular case of low
pressure CVD the reactor consists of a quartz

00:28:20.560 --> 00:28:29.560
tube that you see here this quartz tube that is
connected to a pump ok and the gas inlet is used

00:28:29.560 --> 00:28:36.760
to introduce the reactant gases as well as the
gases needs to purge the system. You typically

00:28:36.760 --> 00:28:44.520
nitrogen is used for purging and the wafers are
loaded through the door which is on the left. So,

00:28:44.520 --> 00:28:53.560
you can open this door and you can load this
sample ok. In low pressure system the wafers can

00:28:53.560 --> 00:29:02.520
be placed closer as you can see here a furnace.
So, this is a three zone furnace that is there

00:29:02.520 --> 00:29:12.800
from the three sides ok top back and bottom ok.
And this particular one actually encompasses the

00:29:12.800 --> 00:29:21.000
quartz tube and this heats up the chamber which
drives the reaction rate faster. Now, what is

00:29:21.000 --> 00:29:28.120
the advantages of low pressure CVD? The first
thing is it is a relatively simple design. So,

00:29:28.120 --> 00:29:34.600
excellent economy it gives you high throughput
and very good uniformity of the thin films.

00:29:34.600 --> 00:29:43.480
But there are some disadvantages also. So,
you can say what are the disadvantages? They

00:29:43.480 --> 00:29:50.960
are susceptible to particle contamination.
So, it requires frequent cleaning of this

00:29:50.960 --> 00:29:59.000
setup and also you need to compensate for gas
depletion effects. Next methods we will see is

00:29:59.000 --> 00:30:09.200
plasma enhanced CVD. Now single wafer process
chambers for plasma CVD look somewhat similar

00:30:09.200 --> 00:30:20.040
to this low power CVD ok. Adjustment figure here
it shows a schematic that tells you how exactly

00:30:20.040 --> 00:30:29.800
single wafer plasma chamber will look like.
So, as with the single wafer LP CVD chambers

00:30:29.800 --> 00:30:36.440
here also the precursor gas is fed to
the chamber using the shower head ok. So,

00:30:36.440 --> 00:30:44.920
you see here and that ensure the uniformity of the
precursor concentration over the wafer phase. So,

00:30:44.920 --> 00:30:52.480
this is where the wafer is kept and this
is basically on a heated plate ok. So,

00:30:52.480 --> 00:31:02.280
the wafer sits on a heated plate and the byproduct
gases are exhausted through this outlet which is

00:31:02.280 --> 00:31:13.320
below the wafer level ok. Now with direct exposure
RF PECVD systems typically employ shower head as

00:31:13.320 --> 00:31:20.360
an electrode for the introduction of the RF energy
to create the plasma that is see here ok.

00:31:20.360 --> 00:31:27.680
The precursor entering the plasma undergoes
electron molecule collisions producing high

00:31:27.680 --> 00:31:35.080
energy excited molecules and molecular fragments
that absorb on the substrate surface and deposit

00:31:35.080 --> 00:31:46.040
the film. So, these are the gas inlets ok. So,
the next method is atomic layer deposition. So,

00:31:46.040 --> 00:31:57.640
atomic layer deposition or ALD it starts by a
pulse ok of metal organic precursor gas into a

00:31:57.640 --> 00:32:04.000
deposition chamber as you can see here this is the
first stage. Under certain conditions the gas will

00:32:04.000 --> 00:32:13.280
react with the surface species of the substrate
in a self limiting reaction that is terminated

00:32:13.280 --> 00:32:20.440
when the surface runs out of the reactants.
So, that is why it is called self limiting

00:32:20.440 --> 00:32:28.640
reaction and the excess gas is purged
in the next step with a neutral gas. So,

00:32:28.640 --> 00:32:35.480
as you can see here nitrogen is being used
for doing the purging you can also use argon

00:32:35.480 --> 00:32:42.840
depending on the process requirements. So, the
second reactant is then introduced into the

00:32:42.840 --> 00:32:50.480
chamber in the third stage. So, here the second
one is introduced and again that starts reacting

00:32:50.480 --> 00:32:58.120
with the surface species like that and the excess
reactant is again purged in the fourth step.

00:32:58.120 --> 00:33:05.000
So, that that gives you one particular cycle
and then it is repeated. So, you can actually

00:33:05.000 --> 00:33:12.040
atomic layer deposition as the name tells you we
can actually deposit layer by layer of atoms and

00:33:12.040 --> 00:33:21.280
grow your thin film. So, in an ideal ALD process
one atomic layer of material is deposited in each

00:33:21.280 --> 00:33:29.200
cycle that is what it does. So, you can actually
precisely control the thickness of the films using

00:33:29.200 --> 00:33:33.640
this particular method. The number of cycles
will then determine the overall thickness of

00:33:33.640 --> 00:33:41.080
the film okay and ALD deposited films are highly
conformal and they can be used for coating and

00:33:41.080 --> 00:33:49.960
encapsulating of complex geometries because
you have complete control on the thickness of

00:33:49.960 --> 00:33:57.160
the films that are being deposited ok. So,
with that we move on to the third method

00:33:57.160 --> 00:34:04.680
of depositing thin films that is epitaxy.
So, when we talk about epitaxy it basically

00:34:04.680 --> 00:34:10.480
this word comes from a Greek word which means
ordered upon. So, epitaxy means basically the

00:34:10.480 --> 00:34:18.200
growth of a single crystal film on top of
a crystalline substrate. So, for most of

00:34:18.200 --> 00:34:23.920
the thin film application which includes
soft or hard coating, protective coating,

00:34:23.920 --> 00:34:31.080
material coating it has little importance.
However, when you go for semiconductor thin

00:34:31.080 --> 00:34:37.640
film technology this becomes very very crucial the
crystalline growth becomes very very crucial.

00:34:37.640 --> 00:34:43.760
So, this is what we mean by crystalline growth.
So, this is not epitaxial, but this is epitaxial

00:34:43.760 --> 00:34:50.760
ok. So, it is a crystalline growth ordered
and crystalline growth. Now note that when

00:34:50.760 --> 00:34:58.320
we talk about the other thin films if they are not
crystalline they are typically amorphous ok. So,

00:34:58.320 --> 00:35:05.320
amorphous films are preferred over thin films
due to the simpler production ok used when

00:35:05.320 --> 00:35:11.000
their properties can meet the application
requirement. So, if you are able to provide

00:35:11.000 --> 00:35:15.800
a amorphous film that can serve your purpose
you stick to that you do not need to develop

00:35:15.800 --> 00:35:21.600
a crystalline film or a very ordered film
because that makes it very expensive ok.

00:35:21.600 --> 00:35:28.320
Now when we talk about the optical coatings
where the refractive index control is crucial

00:35:28.320 --> 00:35:34.640
you actually use amorphous films ok that works for
you. Metal films are commonly used in amorphous

00:35:34.640 --> 00:35:41.760
form for consistent electrical conductivity and
optical reflectivity. While amorphous materials

00:35:41.760 --> 00:35:49.560
they lack distinct electronic band structure due
to their randomness crystals process defines band

00:35:49.560 --> 00:35:56.800
structure with their ordered arrangements and
crystallization can occur through annealing ok,

00:35:57.360 --> 00:36:05.760
but epitaxy is a more formal process for
creating high quality crystalline films. So,

00:36:05.760 --> 00:36:15.440
here is an example of method of epitaxy which is
metal organic CVD. So, this is very very similar

00:36:15.440 --> 00:36:24.560
to LPCVD that you have seen it grows thin layers
by sending special gases over the substrate.

00:36:24.560 --> 00:36:30.600
Now if you see the shower head here ok in this
particular figure it is designed for equal

00:36:30.600 --> 00:36:36.720
distribution of gaseous precursors through the
chamber onto the wafer. So, these are different

00:36:36.720 --> 00:36:46.760
gases which comes in ok. It allows a quick and
uniform diffusion of gas molecules onto a rotating

00:36:46.760 --> 00:36:54.880
heated wafer. So, this the wafer which is being on
a rotating platform and which is also heated. So,

00:36:54.880 --> 00:37:03.560
nitrogen gas is typically used for purging
the system and argon gas can be used as the

00:37:03.560 --> 00:37:10.120
carrier of the metal organic precursors.
These are the wafer loading window this is

00:37:10.120 --> 00:37:17.280
the exhaust ok and this is where the resistance
heater is that heats up the platform ok. So,

00:37:17.280 --> 00:37:27.720
you can actually see that this this particular
wafer at rotates on this platform at a speed up

00:37:27.720 --> 00:37:35.840
to 1000 rpm. The film thickness which is grown
epitaxially that means, orderly ok is mainly

00:37:35.840 --> 00:37:42.680
controlled by deposition time and the growth
rate. And growth rate is also strongly affected

00:37:42.680 --> 00:37:48.160
by the growth pressure in the chamber substrate
temperature and the precursor flow rate. So,

00:37:48.160 --> 00:37:54.560
these are the factors they they actually decide
what will be the growth rate of the film.

00:37:54.560 --> 00:37:59.960
The other method is called molecular beam
epitaxy. This is an epitaxy method where

00:37:59.960 --> 00:38:07.600
thin film deposition of single crystals take
place. So, in this particular method it is

00:38:07.600 --> 00:38:13.280
widely used in manufacturing semiconductor
devices something like transistors and

00:38:13.280 --> 00:38:19.880
it is considered as one of the fundamental
tools for development of nanotechnology. So,

00:38:19.880 --> 00:38:27.480
MBE molecular beam epitaxy is used to fabricate
diodes and and MOSFETs MOS means metal oxide

00:38:27.480 --> 00:38:36.200
semiconductor FETs ok working at microwave
frequencies ok and to manufacture the lasers

00:38:36.200 --> 00:38:45.800
used to read optical disks such as CD and DVDs.
So, I will go into the process soon. So, remember

00:38:45.800 --> 00:38:51.600
that MBE is considered to be one of the cleanest,
but also one of the most technically challenging

00:38:51.600 --> 00:38:59.240
and demanding process because this MBE growth
takes place in ultra high vacuum environment.

00:38:59.240 --> 00:39:07.640
So, this is the chamber which is a ultra high
vacuum UHV chamber. So, an experimental setup

00:39:07.640 --> 00:39:14.840
as you can see here it consists of two or more
Knudsen efficient efficient cells or you can

00:39:14.840 --> 00:39:21.160
say them as K cells which are located at the
bottom of this ultra high vacuum chamber and

00:39:21.160 --> 00:39:26.960
they are aligned towards the center of the
chamber like this ok where the sample holder

00:39:26.960 --> 00:39:32.720
with a substrate. So, this is the sample holder
where the substrate is actually located. Now,

00:39:32.720 --> 00:39:39.840
each individual K cells they contain different
elements in ultra pure solid form.

00:39:39.840 --> 00:39:46.560
So, when you say ultra pure the purity is
typically 99.999 percent ok. So, what kind

00:39:46.560 --> 00:39:54.600
of materials like selenium, bismuth ok they are
used in the thin film synthesis. Now, how it

00:39:54.600 --> 00:40:01.680
works the process of MBE growth starts by heating
this K cells to appropriate temperature until the

00:40:01.680 --> 00:40:12.040
elements in each cell reach a sublimation point
ok. And then the shutters over here as you can

00:40:12.040 --> 00:40:17.240
see the shutters this is open shutter open shutter
and this is a closed shutter. So, these shutters

00:40:17.240 --> 00:40:24.440
are then open and the physical vapor from each
K cell diffuses through the chamber until it

00:40:24.440 --> 00:40:32.320
reaches the substrate and get deposited and this
is how thin films are being formed. Now remember

00:40:32.320 --> 00:40:39.440
that for more uniform growth substrate can be
continuously rotated at low rotation speed.

00:40:39.440 --> 00:40:48.120
So, when I say low rotation speed is typically 1
or 2 rpm ok and by utilizing a stepper motor which

00:40:48.120 --> 00:40:55.000
can be attached to this magnetic manipulator. So,
this is how in this form it can be slowly rotated

00:40:55.000 --> 00:41:03.920
and the electrons which come from this reed gun
ok. So, this is electron diffraction gun. So,

00:41:03.920 --> 00:41:10.960
you can see that it actually incident
electron at a very low angle and you can

00:41:10.960 --> 00:41:17.760
get the defected electron and you can observe
the pattern here. And this pattern can actually

00:41:17.760 --> 00:41:24.760
reveal the quality of the film that is being
developed and also you can measure the film

00:41:24.760 --> 00:41:33.640
thickness starting from single monolayer ok.
So, as I told this particular characterization

00:41:33.640 --> 00:41:42.720
is done by using reflection high energy
electron deflection that is RHEED ok. So,

00:41:42.720 --> 00:41:48.040
in this particular method the final composition
of the film will depend on the temperature and

00:41:48.040 --> 00:41:56.240
the surface atomic structure of the substrate
as well as it will also depend on the flux ratio

00:41:56.880 --> 00:42:02.680
of individual components which are reaching the
substrate. So, this is how you can mix things up

00:42:02.680 --> 00:42:10.920
and get a thin film of a particular composite
material. Selective opening of the structures

00:42:11.640 --> 00:42:19.520
shutters of each K cell they will ensure
growth using only specific elements. So,

00:42:19.520 --> 00:42:25.920
you can also do one by one kind of just by
opening the shutters you can do one layer

00:42:25.920 --> 00:42:30.880
first and then the next layer and so on.
And you can characterize the thin film that

00:42:30.880 --> 00:42:38.760
is getting generated by this RHEED method ok. So,
this particular table sums up all the techniques

00:42:38.760 --> 00:42:45.560
that we have studied till now. So, you can
see the methods are being mentioned here. So,

00:42:45.560 --> 00:42:52.440
evaporation sputtering, pulsed laser deposition,
low power CVD plasma enhanced CVD, ALD, MOCVD,

00:42:52.440 --> 00:42:58.080
and MBE and you can see the parameters
on which they are discussed. So,

00:42:58.080 --> 00:43:06.640
you have substrate temperature deposition energy
pressure step coverage defect density uniformity

00:43:06.640 --> 00:43:11.600
deposition rate and the materials that are used
and what are the different applications.

00:43:11.600 --> 00:43:17.160
So, this actually gives you a very good idea.
And what is important to see here that all these

00:43:17.160 --> 00:43:23.520
methods more or less are very very uniform other
than pulsed laser deposition that does not give

00:43:23.520 --> 00:43:30.560
a very good uniformity. And you can see that
this is pulsed laser deposition is also slow

00:43:30.560 --> 00:43:36.200
and these are first evaporation and sputtering
are first deposition method these are physical

00:43:36.200 --> 00:43:44.720
methods. In chemical methods LPCVD and PECVD
are first methods ok. And you can also see the

00:43:44.720 --> 00:43:51.640
substrate temperature in this case you can have
a wide range in case of physical method in LPCVD

00:43:51.640 --> 00:43:58.440
it should be high PECVD it should be moderate.
And these are the materials that can be used. So,

00:43:58.440 --> 00:44:04.080
when you talk about MBE these are typically
compound semiconductors like gallium arsenide,

00:44:04.080 --> 00:44:11.240
indium phosphide and aluminum gallium
arsenide. MOCVD you can again use the similar

00:44:11.240 --> 00:44:18.320
kind of compound semiconductors. Atomic layer
deposition is useful for alumina, hafnium oxide,

00:44:18.320 --> 00:44:25.560
silicon dioxide and certain metals okay. Then
silicon dioxide can be also deposited by low

00:44:25.560 --> 00:44:33.360
pressure CVD or plasma enhanced CVD okay.
Polysilicon can be done by PECVD ok. Pulsed

00:44:33.360 --> 00:44:39.080
laser deposition can do complex compounds
as we mentioned though it is poor or slow,

00:44:39.080 --> 00:44:45.600
but this method only allows to develop this
kind of complex compounds like PZT YBCO and

00:44:45.600 --> 00:44:53.240
other ferroelectric materials and so on. So,
these are the different applications. So,

00:44:53.240 --> 00:45:00.280
optical thin films as you can see evaporation
and sputtering they are the most commonly used

00:45:00.280 --> 00:45:09.200
for making thin films that can be used for
photonics application ok. Then MOCVD they

00:45:09.200 --> 00:45:15.680
can manufacture optoelectronic devices
and MBE they are also in the useful for

00:45:15.680 --> 00:45:20.400
research and development in epitaxy and
other optoelectronics components. So,

00:45:20.400 --> 00:45:27.640
this particular chart should actually give you
a complete overview of the different processes

00:45:27.640 --> 00:45:33.600
in thin film growth and what are their pros
and cons and what are their applications.

00:45:33.600 --> 00:45:39.940
So, with that thank you for your attention and
we will stop here and in the next lecture we

00:45:39.940 --> 00:45:45.760
will look into the methods of lithography and
pattern transfer of how to make a particular

00:45:45.760 --> 00:45:52.560
pattern on your for your device. And if you
have got any queries regarding this lecture you

00:45:52.560 --> 00:46:24.520
can always drop an email to the similar address
mentioning MOOC on the subject line. Thank you.
