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Chapter 2 discusses nanomaterials, which are materials with dimensions in the nanometric range (1-100 nm) and highlights their unique properties such as increased surface area and quantum effects that enhance reactivity and strength. It classifies nanomaterials based on dimensions and materials, detailing types like nanoparticles, nanowires, and carbon nanotubes, along with their synthesis methods and applications in electronics, energy storage, and biomedical fields. The chapter also covers graphene, its exceptional properties, and various applications, emphasizing its potential in advancing technology.
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Chapter 2
Materials for Electronic Applications
2.1 Nanomaterials ,
Introduction (Nanomaterials are materials whose characteristic length scale lies within the
nanometric range (1-100 nm) at least in one dimension) “The word ‘nano’ has the origin from
the Greck meaning ‘Dwarf". It is one billionth of a nietre (1/10" m), (Nanomaterials are ob-
with any one of the three external dimensions at the nanoscale’) Nanoparticles that are
he incidental byproducts
ly
Ily
naturally occurring (eg; voleanic ash, soot from forest fires) or are U
of combustion processes (eg; welding, diesel engines) are usually physically and chemica
heterogeneous and often termed ultrafine particles. Engineered nanomaterials are intention
produced and designed with very specific properties related to shape, size, surface properties
and chemistry. These properties are reflected in aerosols, colloids, or powders.
area than particle composition
ignificantly from
‘The behavior of nanomaterials may depend more on sui
itself. Two principal factors cause the properties of nanomaterials to differ s
other materials: increased relative surface area, and quantum effects. These factors
or enhance properties such as reactivity, strength and electrical characteristics. As a particle
decreases in size, a greater proportion of atoms are found at the surface compared to those
inside. For example, a particle of size 30 nm has 5 percentage of its atoms on its surface, at
10 nm 20 percentage of its atoms, and at 3 nm 50 percentage of its atomsy Thus nanomaterials
have a much greater surface area per unit mass compared with la tices) As growth
and catalytic chemical reactions occur at surfaces, this means that a given mass 6f material in
nanoparticulate form will be much more reactive than the same mass of material made u
p of
larger particles.
2.1.1 Classification
There are several ways of classification of nanomaterials. Here we discuss two types
This ig the classification based on the number of
1. Classification based on dimensio1
dimensions, which are not confined to the nanoscale range (< 100 nm).
: Here all the three dimensions are in the nanometric range
(a) Zero dimension (0-D)
eg; Nano particles. ybor
(b) One dimension (1-D): Here one of the dimensions is outside the nanometre range
and the other two are within the range eg; Nano wires, fibers and tubes.
47~ Chapter 22"
jons are oul
e dimensions are
layers and coal
(©) Two dimension (2-D): Here wo of lms.
and one is within the range eg: Nane
o dim
(@) Three dimension (3-D): Here all the tubes,
(> 100 nm) eg: Bundles of nano wires
nsions are outst
2. Classification based on materials
defined as mater!
(@) Carb (CNT), wires. SP
Ponent i
grephene.
ese are
based nanomaterials: These af °°
pure carbon eg; Carbon nano tbes
ide the nanoMettic fap
ultinano Inyers.
de the nanomettie ray, ~
Nee
ee
n which the nangg
pheres (fullerenes) go
Ml
are materials made g
r
etal-based nanomil re = dias
(b) Metal based nanomaterials: Metal-base' etc. For example, titaniy,
silver, metal oxides
metallic nanoparticles like gold,
dioxide (TiO).
a erials contain
(©) Nanocomposites: Composite nanomaterials cot
ticles or compounds such as nanosized clays Wii™ @
cles gi 1, mechanical, and/or chem
materi
better physi
(d) Nano polymers or Dendrimers: Dendrimers are ae
branched units. These are tree-like molecules with de
functionalized at the surface and can hide mole
application of dendrimers is for drug delivery.
(c) Biological nanomaterial:
a mixture of simple nanopa.,
ik material. The nanoparg,
properties to the initial buy
scules in their cavities. A direo,
These nanomaterials are of biological origin and are
The i atures of these particle:
used for nanotechnological applications. ‘The important feat Particles
are i) self assembly properties and ii) s
particles, nanostructured peptides. Various
be designed to release compounds under specific cond
delivery systems.
2.1.2 Synthesis of nanoparticles
cific molecular recognition eg; DNA nang
if assembled peptide structures cay
jons and are used in drug
There are many methods available for synthesis of nano-particles. Physical methods include
Laser ablation, spluttering techniques etc. Some chemical methods are disc
Chemical synthesis of nano particles
1. Hydroly:
ssed below
Nano particles of metal oxides can be prepared by the hydrolysis of their
alkoxide solutions under controlled conditions. Commercially important nano particles
of silica (S#O2),titania (T#O2), alumina (Al,O3) are prepared by this method. Hydrother-
mal method and sol-gel method come under this category.
Ti(OR)s + 2H2O + TiO, + 4ROH
Sol-Gel method: The sol-gel method is based on the phase transformation of a sol into
a gel. A sol is colloidal system of nano-solid particles di
loidal system in which liquid droplets are dispersed in
Hydrolysis of metallic alkoxides or metal salts can give
and pH. The sol contains many other impurities
persed in a liquid. A gel is col-
network of solid nanoparticles.
a sol at a suitable temperature
In order to remove impurities sol is
Chemistry for Information Science and Electrical Science (Common for Group A & B)
iii: se naaacaaalaaiilililia aChapter 2: Materials for Electronic Applications
49
teansformed into a get by
by filtration and washing
nanoparticle. For example
aluminium alkoxide by sol
changing the pH or other factors. The gel can be purified
with suitable solvents. The purified gel on drying give solid
aluminium oxide nano particles are obtained by hydrolysis of
-gel technique.
ates +3H,O + Al(OH); + 3ROH
ZA\CowwW, 2 Alo 2u.0
. Reduction: Nano parti Hy Al, 0, + BUC
. Passi Particles of gold and silver can be prepared by the reduction of their
mivcoseleie ; Hons using reducing agents, such as sodium borohydride, ascorbic acid,
Tivided fing tae & With 4 protective agent like thyol, glucose etc. This method can be
}© (Wo, reduction using reducing agents and electro reduction.
Agt +07 > Ag
Reduction using reducing agents: Silver nano particles can be prepared by the following
method. 60 mL of 1 mM AgNO, solution is taken in a beaker, covered with a watch glass and
heated in hot plate, ‘The solution is then stirred using a magnetic stirrer. On boiling the solution,
omL of 10 mM of trisodium citrate is added dropwise, about one drop per second. The beaker
is then closed and kept for some time till the colour of the solution changed to a light golden
colour, Then it is allowed to cool. The solvent can be removed by freeze-drying.
i 4
Elect al Refer 4 ae
§
aheel motes
of Nanomaterials
‘hysical Properties: Crystal structure of nanoparticles is same as bulk structure with
different lattice parameters. The inter-atomic spacing decreases with size and this is due
to long range electrostatic forces and the short range core-core repulsion. The melting
point of nanoparticles decreases with size.
2. Chemical Properties: A large fraction of the atoms are located at the surface of the
anomaterial Which increase its reactivity and catalytic activity. Properties of materials
with nanometer dimensions are significantly different from those of atoms and bulks ma-
terials, This is mainly due to the nanometer size of the materials which render them:
G) large fraction of surface atoms; (ii) high surface energy; (iii) spatial confinement; (iv)
reduced imperfections; which do not exist in the corresponding bulk materials. These ma-
terials have created a high interest in recent years by virtue of their unusual mechanical,
electrical, optical and magnetic properties. Nanophase ceramics are of particular interest
because they are more ductile at elevated temperatures as compared to the coarse-grained
ceramics. Nanostructured semiconductors are known to show various non - linear opti-
cal properties. Semiconductor Q-particles also show quantum confinement effects which
may lead to special properties, like the luminescence.
Applications:
1. Single nanosized magnetic particles are mono-domains. Magnetic nano-composites have
been used for mechanical force transfer (ferrofluids), for high density information storage
and magnetic refrigeration.
2, Nanostructured metal-oxide thin films are receiving a growing attention for the realisa-
tion of gas sensors (NO,, CO, CO2, CH, and aromatic hydrocarbons).
Chemistry for Information Science and Electrical Science (Common for Group A & B). a
ic Applicat;
>: Materials for Electroni to
Chapter 2: Gece
dow layers in solar cells
the production of 25 GEht materia,
3 w
3. Nanostructured semiconductors are used as WH
4. Nano sized metallic powders have been used for
Cuenta Jectronic devices.
, el
5. Carbon nanotube based transistors are used for miniaturizing
6. Carbon nanotube are used for making paper batteries
used for making solar cells.
TiOz is a semicondy,
o-erystalline !
article. Nano TiO can be us.
7. A mixture of carbon nanotubes and fullerenes is
8. Microcrystalline 7:0, is an insulator, whereas nan
Its Band gap can be tuned by controlling the size of nano-P-
for making dye sensitised solar cells. ae
red and functiona|
9. Nanoparticles are used in the fight against tumours, nanostucNONs’, Nye as
surfaces and membranes improved diagnosis and more (ATE ts,
neuro active implants.
tana G: its size. It can
10. Nang Cadmium telluride exhibit different colour depending 4Po? be used
for dyeing fabrics, such nano colourants never fades.
2.1.3. Graphene
hhene is an allotrope of carbon consisting of mono layer of carbon atom Siranged in a
two-dimensional honey comb lattice (fig 2.1). It can be visualized as a single Iyer extracted
from the layered structure of graphite. Graphite is three-dimensional whereas graphene is to
dimensional with one atom thickness. Graphene is defined 2s “the two-dimensional mono.
layer of carbon atoms, which is the basic building block of graphitic materials (1.¢. fullerene,
nanotube, graphite)”.
c
It is considered to Be one of the most promising materials of the century and gained world.
ptical, and mechanical prop.
wide attention due to its extraordinary charge transport, thermal, ©}
| thinnest, strongest material that conducts heat and elec-
erties. It is considered to the lighte:
ticity. It is stronger than diamond and ten times more conducting than copper.
Nobel Prize in Physics 2010 was awarded to Andre Geim and Konstantin Novoselov for the
hene. There are various methods available for the
ground breaking experiments regarding g1
synthesis of graphene, which includes the following,
Mechanical exfoliation method (such as Scotch tape method): Encompasses the repeated
tL
aphite using adhesive tape. This was the method employed by
peeling off layers of
Geim and Novoselov.
Involves the deposition of carbon atoms onto a substrate
of a carbon-containing precursor gas such as methane
. Chemical vapor depositio
(like copper) in the presenc
nv
Silicon cxrbide substrate is heated under ultra-high vac-
icon atoms and deposition of carbon atoms to
. Thermal decomposition on
uum which results in the sublimation of
form graphene layers on the SiC surface.
Graphene oxide reduction method: Graphite oxide, obtained from graphite, is chemically
treated to exfoliate into graphene oxide (GO), which is then reduced to graphene.
mn Science and Electrical Science (Common for Group A & B)
Chemistry for Informatio}Chapter 2: Mi
aterials
‘erials for Electronic Applications 3
ferent techni ; : a
cae (SEM & Tang 28 optical microscope, atomic force microscopy (AFM), electron
mi s EM) are used for the characterization of graphene.
Figure 2.1: Honey comb lattice of graphene
In graphene the carbon atoms are sp? hybridized and are arranged in hexagonal fashion.
Each hexagonal ring comprises of three strong in-plane sigma bonds, with a bond length of
0.142 nm, and a Pz orbitals perpendicular to the plane. These orbitals hybridize together to
form two half-filled bands of free-moving electrons, w and x*, which are responsible for most
of graphene’s notable electronic properties.
[Link] Properties of graphene
Electrical conductivity: Graphene has high electrical conductivity. Graphene, being two-
dimensional material shows Quantum Hall effect. They behave as massless rel
(Dirac fermions) which allows the electron speed comparable to light. They ha
mobility compared to metals.
ivistic particles
e high electron
Mechanical strength and elasticity: They possess high clastic modulus and strength. It is
200 times stronger than steel. Graphene is highly is flexible and can be stretched by up to 20%
of its original length without undergoing structural damage.
Thermal Conductivity: Graphene exhibits excellent thermal conductivity and is highly efti-
cient for heat dissipation and thertnal management applications.
Optical: Graphene absorbs only 2.3% of incident light over a broad w:
hence makes it suitable for applications in transparent electrodes for dis
screens ete.
welength range and
ays, solar cells, touch-
Surface area: It has high surface area due to its single-atom thickness and hence useful for
applications in energy storage devices.
Graphene is chemically inert, stable and biocompatible also.
Chemistry for Information Science and Electrical Science (Common for Group A & B)Chapter 2; Materials for Electronic Applications
2 Applications of graphene
1, Electronics:
(a) Due to its lower resistance and higher transparency, graphene-based thin film can
be used in touchscreens, which is found to be superior than indium tin oxide.
(b) Smaller size transistors can be developed using graphene which shows better per-
formance.
2. Energy storage:
(a) Graphene incorporated lithium-ion batteries have longer life span, faster charging
time and higher capacity.
(b) It can improve the efficiency of hydrogen fuel cell by lowering fuel cross over (fuel
permeating through the electrolyte or membrane to the opposite side of the fuel
cell).
(©) Graphene is used in supereapacitors to provide high energy densi
3. Biomedi al
(a) Suitably functionalized graphene can be used to carry chemotherapy drugs to cancer
cells.
(b) Graphene-based biosensors are highly sensitive when detecting DNA, ATP, dopamine
etc,
4. Composites and coatin
(a) By combining graphene with paint, a unique graphene coating is formed which will
effectively prevent rusting.
(b) Graphene in the carbon-fibre coating of aircraft's wing resists impact better and
consumes less fuel.
(c) Graphene-based composites and coatings could play a significant role in improving
sports equipment for skiing, cycling etc.
5. Environmental:
(a) Graphene based membranes can purify water in a more efficient, cheaper and envi-
ronmental friendly way.
(b) It can be used in filters and coatings to remove pollutants and toxins from the air.
2.1.4 Carbon Nanotubes
Carbon nanotubes (CNTs) are allotropes of carbon with cylindrical nanostructures. They are
conceptually graphene sheet rolled into a tube. CNTs were discovered in 1991 by the Japanese
electron microscopist Sumio Iijima who was studying the material deposited on cathode dur-
ing the arc-evaporation synthesis of fullerenes. There are different methods available for the
synthesis of CNTs with different structure and morphology. Are-discharge method, laser ab-
lation/evaporation method, chemical vapor deposition method etc. are the commonly used
methods for the synthesis of CNTs. .
Chemistry for Information Science and Electrical Science (Common for Group A & B)53
Carbon nanotubes are one-dimnan, :
and are generally only a fee aamensional nano particles with diameter measuring 1-50 nm
nanoscopic hollow fibre or patisrometres in length, They are molecular scale tubes and are
acterised by high tensile strempan ceo His 10" tines thinner than hums hairs They are chin,
ae arstau lena (oe a ength and according to structure are conductive or semi conductive,
‘ ; es stronger than steel, but i
ate fa . but o SAG, ion, the
conduct Heat and electricity far better than capper NAH As dense, In wdlition, they
[Link] Classification of CNT
here are t . 5
‘There are two types of CNT hamely single-walled (SWCNT, one tube) and multi-walled
(MWECNT, several concentric tubes). Both or
v S). h of these are typically a a vi
and several micrometres to centimetres long a
:
SWCNT can be visualized as rolled-up tubular shell of graphene sheet, Based on the vari-
ations arising from the specific orientation and rolling of g aphene sheets, SWCNTs are clan-
rl lr e..:—rt—“itiOCOOC~C*C@COCSC~Ci*Ci*C*SCS exhibit a symmetrical
Oe te rll Ge allen ith te hee gona! iniiles oF phene, resulting in
maleate Slezad into. on ths aie: lad, gre Gres vic rolling ax
along the zigzag pattern of the graphene lattice, leading to edges that consist solely of zig
eens he rete Gy oll, ale at tends oe cs
Eraphene lattice, resulting in unequal edge lengths and a helical structure, ‘The optoclectronic
Properties of carbon nanotubes vary s gnificantly with molecular structure and diameter of the
tube.
MWCNT is a stack of graphene sheets rolled up into concentric cylinders, There are three
different models proposed for MWCNT namely Russian doll model, Parchment model and
mixed model. In Russian doll model, sheets of graphene are arranged into concentric cylinders
whereas in Parchment model single graphene shect is rolled around itself, similar to a scroll of
parchment. Mixed model is a mixture of both Russian doll and Parchment model. Classification
of CNTs is shown in figure 2.2
Carbon Nanotubes
GP. walled CNTs Multi walled CNTs
ee
Armchair Zigzag Chiral. Russian doll Parchment Mixed
B a) ' model mode!
Figure 2.2: Classification of carbon nanotubes
Chemistry for Information Science and Electrical Science (Common for Group A & B)telescoping po ufiaterto
lescor fea ‘Chapter 2: Ma
est materials. Single walled jay,
y seit sompressing HALTOM ten”
mater fe formed between the ing,
P without deformation, My
{bit telescoping Property,
2.14.2 Properties of Carbon Nanot
Strength and hardness: ‘They are the a
otubes (SWNTS) are used for synthesizing super han!
Perature. High stre sould be attributed to the covil
vidual carbon at ny withstand a pressure UPE
walled 1 ed inner ®
ptubes (MWNT) without inter connects
vest and
ells exh
aor than metals. ELTON tray,
be annel- Ballistic Trang
thre F Por,
fy vith relatively HID temp,
ity is
rough sm200!
tiv
Electrical conductivity: ‘Their clectrical conduc
8 through a CNT behaves like a wave travelling condi
MWNTs with interconnected inner shells show superee
atures,
er than metals. Al nanotubes
od insulators laterally tg
is found 16 bg
9 is bet
tube but
arbon nanotubes
Their thermal conductivity alse
along the
stability of €
‘Thermal conductivity:
re expected to be very good thermal conductors
the tube axis- Ballistic Conduction. The therm
upto 2800°C in vacuum and about 750°C in ait,
[Link] Applicatio rates
nn made that operates at room,
ve bee! ‘
electronic devices.
1. Electrical circuits: Nanotube bas
temperature, Carbon nanotubes are used for min!
_ optimised electrical
> applications.
and thermal properties
2. Energy storage: Due to high surface a
they are widely employed in energy stor:
¢ 1 paper-thin shee
A paper battery is a battery engineered £0 use & Paper thin sheet
ves a steady power output,
4 quick explode of high
(@) Paper Batter
of cellulose infused with aligned carbon nanotubes. IC gives
9 functions as a super-capacitor which give 3
This battery
energy. ;
(b) Solar Cells: CNT-fullerene hybrid s cell is formed by a mixture of carbon nan-
otubes and fullerenes, Electrons trapped inside fullerenes are excited by sunlight
leading to the flow of this electrons, which produce the current. CNT acts as the
conductive pathway.
(©) They are used for making ultra-capacitors which provide a large surface to store
electrical charge
3. Aerospace and automotive industry: Due to easier molding, high strength, stiffness,
and reduced weight, CNT polymer composites are preferred for aerospace and automo-
tive applications.
ge of hydro-
4. Research is also being carried out to assess the ability of CNTs for the stora
gen,
2.1.5 Carbon Quantum Dots (CQDs)
Carbon quantum dots are zero-dimensional small carbon nano particle. It consists of ultra-
fine, distributed, quasi-spherical carbon nanoparticles with size less than 10 nm. Recently
they have attained much attention due to their good solubility and strong luminescence proper-
ties. CQDs are found to be much more superior than traditional semiconductor quantum dots
Chemistry for Information Science and Electrical Science (Common for Group A & B)Chapter 2: Matenals for Electronic Applications
—_———
due to its lower molecular weight, reduced toxicity, ease of surface functionalization, cost-
effectiveness, exceptional fluorescence stability, tunable emission wavelengths, strong biocom-
patibility etc.
Carbon quantum dot was first discovered by Nu et al. in 2004 accidentally during the purifi-
cation of single-walled carbon nanotubes via electrophoresis. It can be synthesised using (wo
main methods: "top-down" and "bottom-up", The top-down approach involves breaking down
large carbon structures into small CQDs using techniques like chemical oxidation, laser ab-
lation. are discharge, and electrochemical synthesis, The bottom-up method invalves building
CQDs from small carbon molecules through processes like hydrothermal synthesis, microwave-
assisted synthesis, and pyrolysis, which allows control over their size and shape. Synthesised
particles can be purified using electrophoresis, centrifugation, dialysis, column chromatogra
phy ete.
[Link] Properties
Optical: CQDs shows absorption mainly in the UV region which can extent to the visible re-
gion also. They exhibit strong fluorescence, photoluminescence and chemiluminescence which
makes them useful in imaging and sensing applications. They can be excited by various wave-
lengths of light and often display tunable emission spectra.
Stability and biocompatibility: CQDs show excellent photostability and biocompatible with
less toxicity than other quantum dots and hence suitable for medicinal and biological applica
tions.
[Link] Applications
1. Biomedical:
(2) Due to its fluorescence property, better biocompatibility and low biotoxicity they
are employed in fluorescent bioimaging.
(>) CQDs are used as biosensor carriers because of their solubility in water, tunable ex-
citation property, excellent biocompatibility and photostability. CQDs-based biosen-
sors can visually monitor various substances including glucose, copper, phosphate,
iron, potassium, and nucleic acids.
(c) They are used in drug delivery systems also.
2. Optoelectronics:
(a) CQDs have shown potential in enhancing the performance of DSCs due to their
stable light absorption properties, photostability and low cost. By creating CQD-
bridged dye/semiconductor complex systems, CQDs improve the photoelectric con-
version efficiency significantly.
(b) CQD-based hybrids have been identified as excellent materials for supercapacito:
CQD-fuO; hybrid show remarkable electrochemical performance.
3. Lighting: Due to their stable light emitting, low cost and eco-friendliness they are used
as LED materials. Switchable electroluminescence behaviour makes it useful for devel-
oping colourful LEDs.juyptet ? Mawes Ny
chante
56 vataty tie depeilAton af oy
a priate tty rate oligo Kone
adtyo tinprove t snshit al fae nle Nt aLiYige
4. Knvironmental: CONS ea NT ay 9 ate ay bea clown HAT Orga
r 42 ,
ke
pollutants and dyes in water
enhances the eftivieney of phot
compounds,
oe ataly sts
Jopa/ti2s) enlanes photowatas
py, comptes (CQDS Vig
pp8 THO. ©
«Catalysts: CQDs-moditied P25
hydrogen evolution,
a
opartietes nto OF CAH00 Htgyys
fulaniaated in thelr Nobel Pye
ved alter Richatd Huckmninge
timex called bucky hay,
2.1.6 Fullerenes a
J elosedd cae
Fullerenes are zero-dimensional, hollow, aut ep saalley
‘The discovery of fullerenes in LO8S by Cull, cv 2a), are wn
in 1996, Fullerenes, or Buckminster rulterene i Fad ate SOUT
Faller the architect and designer of the geodesic
Figure 2.2: C60 “bucky ball” fullerene
toms in the spherical carbon
Fullerene molecules are denoted based on the number of carbon nthe § r
ball. The smallest fullerene reported with twenty carbon atoms as C20 followed by C24
and C28 analogues. Each fullerene generally contains 12 pentagonal and (n/2-10) hexagonal
rings, where n > 20.
C60 fullerene, known as the Buckminster fullerene is the primarily discovered and most
widely studied form of fullerene. In 1990, a technique to produce larger quantities of C60 was
developed by heating graphite rods in a helium atmosphere. ‘The sooty material formed by
smaller quantity of C70 (rugby
condensation of vaporized carbon consists of mainly C60 with
ball shape) sand traces of fullerenes consisting of even number of carbon atoms up to 350 oF
above. It is composed of fused pentagonal and hexagonal carbon rin; It contains 12 five
membered rings (12 x 5= 60 atoms) and 20 six membered rings, possess perfect icosahedral
mmetry. The geometry is same as that of soccer football.
Chemistry for InformationChapter 2: Materials for Electronic Applications 7
Fullerenes are stable, but not totally unreactive, The sp hybridized carbon atoms, which are
at their energy minimum in planar graphite, must be bent to form the closed sphere or tube,
which produces angle Strain. The characteristic reaction of fullerenes i: electrophilic addition
at 6,6-double bonds, which reduces angle strain by changing sp? hybridized carbons into #p?
hybridized ones. The change in hybridized orbitals causes the bond angles to decrease fron
about 120° [Link] sp? orbitals to about 109.5° in the sp? orbitals, This decrease in bond angles
allows for the bonds to bend less when closing the sphere or tube, and thus, the molecule
becomes more stable,
[Link] Properties
Physical: | Fullerenes are extremely strong molecules, able to resist great pressures - they will
bounce back to their original shape after being subject to over 3,000 atmospheres. This property
makes fullerenes become harder than steel and diamond. An inter sting experiment shows that
Fullerenes can withstand collisions of up to 15,000 mph against stainless steel, merely bouncing
back and keeping their shapes. This experiment demonstrates the high stability of the molecule.
Solubility: Fullerenes are sparingly soluble in many solvents. Common solvents for the
fullerenes include aromatics, such as toluene, and others like carbon disulfide. Solutions of
pure buckminster fullerene have a deep purple color. Solutions of C70 are a reddish brown.
‘The higher fullerenes C76 to C84 have a variety of colors.
Electrical: Fullerenes are normally electrical insulators, but when crystallized with alkali
metals, the resultant compound can be conducting or even superconducting.
Light absorption: Fullerenes absorb strongly in the UV and moderately in the visible regions
of the spectrum.
Chemical: The carbon atoms within a Fullerene molecule are sp? and sp? hybridized, of
which the sp? carbons are responsible for the considerably angle strain presented within the
molecule. C60 and C70 exhibit the capacity to be reversibly reduced with up to six electrons.
[Link] Applications
+ 1. Coatings and lubricant:
(a) Fullerenes are used for making durable, high-performance coatings that resist wear
and corrosion.
(b) Fullerenes are used as miniature ‘ball bearings’ to lubricate surfaces. C60 can be
used used as excellent microscopic ball bearings, lubricant and catalyst.
2. Biomedical:
(a) Fullerenes can be used to deliver drugs to specific cells or tissues due to their ability
to form stable complexes with various molecules. :
(b) Fullerenes can be used as contrast agents in imaging techniques such as MRI or
ultrasound.
3. Energy storage:
Chemistry for Information Science and Electrical Science (Common for Group A & B)(Cpe tee eer ante Plies
ay ny
Joyed energy storag eS due to, te
~ tives are empl
(@) Fullerenes and their derivate
electrical conductivity and s'
drogen.
(b) They can be used to store hydroge!
4. Environmental: lutants and contaminants,
ral of pol
(a) Used in water treatment for the remov:
ins and pollutants.
' al toxins an
(b) Used in sensors for detecting environment
2.2 Polymers
sses obtained by the covalent link,
rs, The repeating chemical unj,
mer in a polymer then it is known
‘The number of repeating units
two or more different monoms”
Polymers are molecules with large molecular ma:
several small repeating chemical units called monome
be same or different. If there is only one type of mono! ,
homopolymer, eg. Polyethylene, Poly propylene ee ie _
called the degree of polymerization. A co-polymer is ma¢ :
species, eg. ‘butadiene-styrene (BS) Acrylonitrile Soe ners Fa ©n the
types of polymerizations, polymers can be broadly divided into addition (£8: PVC. neoprene
gic.) and condensation polymers (PET, bakelite etc). Two special clSSSe5 Of Polymers vg,
fire-retardant polymers and conducting polymers will be discussed in .pter.
Be of
may
2.2.1 Fire-retardant Polymers
gee
‘Methylol phenol Novolac
Sees
Hy
Bb oS
on
Bakelite
Poy O KTH
Polyimide
Polybenzoxazole
Figure 2.4: Examples for non-halogenated fire-retardant polymers.
Chemistry for Info
for Group A & B)Chapter 2: Materials for Electronic Applications 59
Most of te Polymers contain organic compounds as monomers and are flammable. [Fire
retardant polymers resist ignition and slow the spread of flames. Nitrogen based polymers
such as melamine-formaldehyde, inorganic polymers such as silicone polymers ete comes un
der the category of fire-retardant polymers. {Phenolic polymers such as novolac, bakelite ete
and aromatic heterocyclic polyimid:
polybenzoxazoles ete are also examples of intrinsically
fire-resistant polymers\(t
Inorganic additis
such as aluminium hydroxide, magnesium hydroxid
phate etc. and organophosphorus compounds (such as DMMP, BDP)
polymers to enhance their fire resistance.
mmmonium polypho
1 be incorporated into
Halogenated polymers are also fire
system which contains radicals such a
rdant polymers (Fire is a free radical chain reaction
i H*, OU", OOH*, CH ete. In the ease of halogenated
polymers like PVC, Poly brominated styrene ete halogen radical (Cl, Br*) is also introdt
into the fire, which combines with H radical and OH radic
HX and HOX (where X can be Cl or Br) respectivel
Among halogens Bromine is found to be mote efte
s to form stable mole:
resulting in quenching of cha
ve in quenching fire”)
Examples of chlorine containing polymers are polyvinylchloride (PVC) and chloroprene rub:
ber (neoprene). Poly(bromo styrene) and brominated butyl rubber are examples of bromine
containing polymers. Brominated butyl rubber is synthesised by the bromination of butyl rub-
ber. Structures of the polymers are given in fig 2. 5.
NCH, ==CHCL —~— for, ont
| n
Vinyl chloride pve i
nCHy-—=E—cH CH, —— -fon— CH—CH,
cl cl
‘Chloroprene Neoprene
.
a —
Br Br
Bromostyrene Poly bromostyrene
CH,
\l
CHC HoH
Br
Brominated butyl rubber
Figure 2.5: Examples for halogenated fire-retardant polymers.
Chemistry for Information Science and Electrical Science (Common for Group A & BYjmeriats for Bleetonle Apptio,,
Chapter 2: MP i
60
yee they FeMAIN HN The egy ¢
tion,
abustion oF de;
oh recon
ducts during
not mu
Use of halogenated polymers are
logenated poly oie DY
ment for Jong periods and can releas 1
‘nt for Jong periods and can rel mpounds, especially tho.
“phey will release haloxey, 6%
on
openated ¢
waited polymer. ieee Janne,
Note: Apart from these haloge I as fire retard
heen used A®
taining bromine or chlorine,
and interfere with the combustic
process.
J dipheny! ethe
jolybrominat " ers (py
131). Pe rodosdeeane GIBCD). polyey,
rormacture of the COMPOUNS are
h
hon
ols (PI
Examples include polybrominated biphenols ( ‘
Biv
DEs), tetrabromobisphenol AC BBPA) ond
nated biphenyls (PCBs) and trichloroethylene
in fig 2.6,
‘TBBPA
puts Pape
ren
7
Hy
cp
Figure 2.6; Halogenated fire-retatrdants
2.2.2 Conducting Polymers
In general, polymers are found to be insulators. With in the past few years, a new class of
organic polymers have been synthesized which possess remarkable ability to conduct electrical
current.(A polymer which can conduct electricity is termed as conducting polymer. [Among
many polymers known to be conductive, poly acetylene, poly an and poly pyrrole have
been studied most} However, the conductive polymer that was actually launched this new field
was poly acetylene.
ation: Conducting polymers can be classified into following types
[Link] Intrinsically conducting polymers
‘These polymers have extensive conjugation in the backbone which is responsible for con-
ductance. This is again classified as
Chemistry for Information Science and Blectrical Science (Common for Group A & B)Chapter 2: Materials for Electronic Applications 41
Conducting polymers
Invinsically Conducting Extrinuically Conducting
——J ————aer —
Conductive Blended
Conducting Dopedcondveting | | clement conducting
polymers Raving polymers. filled polymers
Conjugated 7 electrons polymers - an
1. Conjugated = - electron conducting Polymers:
A key property of a conducting polymer is the presence of conjugated double bonds
along the backbone of the polymer. The orbitals of conjugated 7 - electrons overlap
over the entire backbone of the polymer, resulting in the formation of valence bands and
conduction bands, which extends over the entire polymer molecule. The highest occupied
band is called valence band and lowest unoccupied band is the conduction band, “These
bands are separated by significant band gap. Thus electrical conduction would occur
when electron from valence band are excited to conduction band either thermally or
photolytically eg. polyacetylene and polyaniline.
Addition polymerisation Xf ~P
nu _
acetylene potyacetylene
[0] CY o. -
n € yin, endl eae it 4 nH,0
cnidaune polymeriation ; a
aniline poly aniline
rer
hamisuy for Information Science and Electrical Science (Common for Group A & B)62 Chapter 2: Materials for Electronic Application,
2. Doped conducting polymers:
In comparison to conventional polymers the conducting polymers with conjugated x.
electrons in their backbone can be easily oxidized or reduced as they have low ionization
potentials and high electron affinities, ie; their conductivities can be increased by creating
positive or negative charge on polymer backbone by oxidation or reduction. This process
is referred to as ‘Doping’ and are of two types
(a) p-doping: It is done by oxidation process. In this process some electrons from x
~ bond of the conjugated double bonds are removed and the holes so created can
move along the molecule, ie; the polymer becomes electrically conductive. The
radical cation produced is called ‘polaron’. The polarons are mobile and can move
along the polymer chain by rearrangement of double and single bonds and hence
the polymer become conducting. The oxidation process is generally brought about
by Lewis acids such as FeCl. ,
ale
WA AA SA FO
{
poreorte
RADA
ommestion of «poor thong confit pds chain by shifting of duble bonds
Figure 2.7: p-doping (polaron movement)
(b) n-doping: In this type of doping some electrons are introduced into the polymer
having conjugated double bonds by reduction with Lewis bases like lithium, sodium
naphthalide etc. The reduction of polyacetylene by a Lewis base leads to the for-
mation of anion called ‘polaran’ and bipolaran in two steps.
Pete
Propesation of a hpoloran through a conjugated polymer chain by shifting of doubt bonds
Figure 2.8: n-doping (polaran movement)
or Group A & B)
Chemistry for InfoChapter 2; Materials for Electronic Applications
ae polymers
“Repeating unit
Trans-poly acetylene A277
Poly anili .
oly aniline iin
n
BF, ;
Pos $~-Os-
oe " Helo, |s00-7500
200
[Link]. Extrinsically conducting polymers
There are conducting polymers whose conductivity is due to the presence of externally added
ingredients in them, 7
1. Conductive element filled polymer: These are polymers which are filled with conduct-
ing elements such as carbon black, metallic fibers, metal powders etc. The polymer acts
as a binder to hold the conducting elements together. These polymers are, (i) low in
cost, (ii) light in weight (iii) mechanically durable and strong, (iv) easily processable in
different forms, shapes and sizes. This type is used in making computer key boards.
2. Blended conducting polymers: These polymers are obtained by blending conducting
polymers with conventional polymers. These polymers possess better physical, chemical
and mechanical properties. 2 pry) _ py
- PYC blend
2.2.3 Polyaniline (PANI)
The oxidative product of aniline under acidic conditions is known as aniline black from 1862.
Since 1980s polyaniline captured the intense attention of the scientific community due to the
rediscovery of high electrical conductivity.
Chemical synthesis
1. Chemical method: Aqueous solution of ammonium per sulphate is added slowly to a
solution of aniline dissolved in dilute hydrochloric acid at a temperature of 5°C’ under
agitation. After an hour a precipitate is formed, which can be removed by filtration. The
polymer thus obtained is washed with ammonium hydroxide solution and dried.
2. Electro-chemical method: When thin film or better ordered polymer is required an elec-
trochemical oxidation method is preferred. It is done by dipping platinum foil electrodes
on acidified aqueous solution of aniline and a potential of 0.7 V is applied, then polyani-
line film is formed on the surface of the positive electrode.
Properties Among various conducting polymers, polyaniline (PANI) is a unique and promis-
ing candidate for potential applications because of its stability, in air and solubility in some
Chemistry for Information Science and aaod aid eee
Pe a —— + 1 H,0
( . —_—
a é Ninty
oly aniline
aniline ah
1 Ir also exhibits dramatic changes in its electronic structure and physical prop-
oryumte solvents, [also exhibits drama
tracted much attention for its magnetic behaviour
tion
cently PANI |
cities on protonation, Recent : beat
vo aveshibity high spin density and ferromagnetic spin-spin inter:
the colour change associated with polyaniline in different oxidation states can be used in
sors and electrochromic devices. Polyaniline is more noble than copper and slightly less
sensors and electrochromic devices e ; ‘ |
hohle than silver whieh is the basis for its broad use in printed circuit board manufacturing and
good conductor comparable to copper, whereas
in corrosion protection, Doped poly at
the original form is a ‘ondui
Applications
\
As electrode material for rechargeable batteries.
2. In the dissipation of static electric charges in metallic containers.
\. As shield in complex electronic circuits and electromagnetic radiations.
4. In biosensors and solar energy absorption.
2.2.4 Polypyrotle 0!
Polypyrrole is one of the most promising m
is an inte
‘terial with multifunctionalised applications. It
ducting polymer with conjugated double bonds.
Preparation: I can be prepared by electrochemical or chemical polymerization.
1. Electro
hemieal method: Polypyrrole can be synthesized by electrochemical technique
4s follows, By the electrolysis of pyrrole (0.06 M) in aqueous acetonitrile solution us-
tng platinuny electrodes and tetraethy! ammonium boron tetrafluoride as the supporting
electrolyte (0.01 M), the polymer will be precipitated as a blue black film on the anode.
2, Chemical method: Polypyrrole can be synthesized by chemi
tion technique using monomer pyrrole and
al oxidative polymeriza-
ammonium per sulfate as oxidant in the ratio
ied out in a beaker by mixing 0.1 M aqueous
nd 0.1 M of ammonium per sulfate in 1:1 ratio for 3 hrs. The polymer
precipitates out, The PPy tilms can also be deposited on pre-cleaned glass substrate,
11 The chemical polymerization can be e;
solution of pyrrole
Chemistry for Information Science and Ele
ical Science (Common for Group A & B)Chapter 2: Materials fi
0]
[0] re \ ee +n 1,0
oxidative polymerisatio Ny dn
8
polypyrrole
pyrrole
nd mechanical properties. It has good
sistance was found to decrease
Properties: PPy has excellent electrical, the!
environmental stability and higher conductivity. The electrical
as temperature increases and hence conductivity increases, The decrease of resistance is due (0
the increase of efficiency of charge transfer in PPy with increase in temperature, PPy films are
yellow but darken in air due to oxidation, Doped films are blue black depending on the degre
of polmerisation and film thickness. They are amorphous and give weak diffraction, Pare PPy
san insulator while its oxidative derivatives are good electrical conductors,
Applications of Polypyrrole (PPy)
1. Polypyrrole is used mostly in biosensors and immunosensors, because of its biocomp
ibiliy
mechanical match
Compared with metal and inorganic materials, doped PPy has bette!
with live tissue, resulting in its many applications in biomedical field.
3. Ithave applications in issue engineering.
sensitized solar cells.
4, Itis also employed as counter electrodes in dy’
2.2.5 Applications of conducting polymers
1. In Rechargeable Batteries: The conducting polymers can be used as cathodes and solid
plications. These batteries have high
re small in size.
electrolytes in batteries for automotive and other
reliability, light weight, non leakage of electrolyte and a
niline show different colours in different oxidation
1 be used to produce “smart windows” and cle
indows which change colour in ri
Some conducting polymers like po!
forms. This electrochromic property ca
trochromic displays. [Smart windows are the
to sunlight or temperature changes}
yonse
also used in electro-luminascence OLED displays like TV, mobile phone etc:
These are
4. Inanalytical sensors: These polymers are used for making sensors for pH, O2, NO; SC
and glucose detection.
eg. In Al, polymer/Au photovoltaic cells,
In photovoltaic device:
6. Inclectronics: It can be used in Light Emitting Diodes (LEDs), electromagnetic shield-
ing. electron beam lithography, ete.
Chemistry for Information Science and Electrical Science (Common for Group A & B)66 chapter 2: Materials for Electronic Application,
ee SS
2 ne —
2.3 Organic Light Emitting Diodes (OLEDs)
ng diode (LED) in which the emis.
d which emits light in response ,,
nic light - emitting diode (OLED) is a light-emitti
sive electroluminescent layer is a film of organic compound Whit MTT A ae
an electric current. This layer of organic semiconductor is situated DF ATEN A EAN es: a
least one of these electrodes is transparent. There are two main famil * (those
5 le.
employing conducting polymers (ii) those based on small molecul
is HOMO-LUMO transitions) The
(Principle: B pancie g: v1 LED 2
(Principle: The principle of conjugated polymer ee iting elecirocheTied ort
basic principle of small molecule OLED is the creation of.
(LEC) on adding mobile ions to an OLED.
OLED employing conducting polymers |
A typical OLED is composed of a layer of organic materials situated between two elec.
trodes, the anode and cathode, all deposited on a substrate. “The organic molecules are elec.
trically conductive as a result of delocalization of 7-electrons caused by conjugation of the
molecule. These materials have conductivity levels ranging from insulators to conductors, and
are therefore considered organic semiconductors. The highest occupied and lowest unoccu-
pied molecular orbitals (HOMO and LUMO) of organic semiconductors are analogous to the
valence and conduction bands of inorganic semiconductors like silicon.
The organic compounds used in OLEDs include derivatives of poly(p-phenylene vinylene)
(PPV) and polyfluorene. Substitution of side chains onto the polymer backbone may determine
the colour of emitted light, |
RR
\
- OO, |
Poly(para-phenylene vinylene}
polyfluorene
Construction: Many modern OLEDs incorporate a simple bilayer structure, consisting of a
conductive layer and an emissive layer. A typical organic light emitting diode (OLED) structure
consisting of a glass substrate, a indium tin oxide (ITO) anode, and an organic bilayer diffused
into a metallic cathode, as given below. The organic bilayer consists of a hole transport layer
(HTL) and an emitting/electron transport layer (EML/ETL). The emissive layer and the con-
ducting layer is made up of organic molecules (both being different). The emissive layer used
in an OLED is made up of n-type polymer molecules, out of which the most commonly used
is polyfluorene. The conducting layer is made up of p-type polymer, and the commonly used
component is polyaniline.
Chemistry for Information Science and Electrical Science (Common for Group A & B)layey ©
Figure 2.9: Schematic of a bil
radiation, 4. Conductive layer, 4, Metal cathode (
Working: To make an OLED light up, we simply attach a voltage (potential difference)
across the anode and cathode. As the electricity starts to flow. the cathode receives electrons
from the power source and the anode loses them, Now we have a situation where the added
electrons are making the n-type emissive layer negatively charged, while the p-type conductive
layer is becoming positively charged. Positive holes are much more mobile than negative elec~
they jump a the boundary from the conductive layer to the emissive layer. When a
gle electron z-bond) meets an electron, the two things cancel out and release a brief
burst of energy in the form of a quantum of light or a photon, in other words. This proces:
is called recombination, and because it's happening many times a second the OLED produces
continuous light for as long as the current keeps Nowing.
‘
Note: In conventional LED like GaAs and GaN electrons are more mobile than holes so p=
region is the emissive layer.
‘Small-molecule OLED
amdwiched between electrodes. The organic layers adja-
cent to cathode and anode are the electron transport layer (ETL) and the hole transport layer
(HTL), respectively. Emissive layer (EML) usually consists of light-emitting dyes or dopants
dispersed in a suitable host material, Molecules like quinacridone derivatives are often used.
Aluminium quinacridone (Alg3) has been used as a green emitter (fig.2.10).
It consists of three organic layers
Advantages of OLED
1, The manufacture of OLED is highly economical and is more efficient than LCD and flat
panel screens. Eo ot
2. OLED display can be printed cloths and fabrics by ink jet printing. This technology will
help in carrying huge displays in our hands.
3. There is much difference in watching a high-definition TV to a OLED display. As the
contrast ratio of OLED is very high (even in dark conditions), it can be watched from an
angle nearly 90 degrees without any difficulty.
Chemistry for Information Science and Electrical Science (Common for Group A & B)
Ewissive
Conducttve
layer HTL)
deh
TL)
(Pelyf tnorendMaterials for Electronic Applications
68
Figure 2.10: Aluminium quinacridone (Alq3)
4. No backlight is produced by this device and the power consumption is also very less.
5. OLED has a refresh rate of 100,000 Hz which is almost 9900 Hz greater than an LCD
display.
6. The response time is less than 0.01 ms. LCD needs a response time of 1 ms.
klitte the applecattons of OLED-
2.4 Dye-Sensitized Solar Cells (DSSCs)
Escalation in global population and energy consumption demand the urgent shift towards
renewable energy sources. Among various renewable energy sources, solar energy stands out
as the most practical due to its efficiency, low fabrication cost, and environmental benefits. A
solar cell is an electrical device that converts the energy of light directly into electricity by the
photovoltaic effect. Conventional solar cells use crystalline silicon semiconductors. It works
on the principle of photovoltaic cell. Here photons of light knock electrons from atoms within
the semiconductor material, creating an electric current.
DSSCs were developed as an efficient and environmentally benign alternative to silicon
based solar cells. (A dye-sensitized solar cell (DSSCs) is a photoelectrochemical cell. which
converts solar light absorbed by the dye to electric energy. It is a thin-film solar cell. ]
2.4.1 Construction of Dye-sensitized solar cells
ADSSC mainly consists of a substrate, transparent conductive oxide layer (TCO), semicon
ductor metal oxide nano particle, organic / inorganic dye, electrolyte and counter electrode.
Substrate is generally made up of glass or flexible transparent plastic, TCO is coated on the
substrate.
Transparent conductive oxide (TCO): Thin film of Indium Tin Oxide (ITO) or Fluorine-
doped Tin Oxide (FTO) acts as TCO.
Semiconductor metal oxide nano particles: Semiconducting metal oxides with high surface
area and wide band gaps are used in DSSCs. TiO; is the commonly used metal oxide. Other
metal oxide like ZnO and SnO? are also used.
Chemistry for Information Science and Electrical Science (Common for Group A & B)Chapter 2: Materials for Electronic Applications ba
Dye/photo sensitiser: Surface of the metal oxide particle is coated with dye molecules.
ese dye molecules are responsible for absorbing sunlight and inject the photoexcited elec
trons to the conduction band of the semiconductor, Dye-sensitized metal oxide semiconductor
acts as the anode, Ruthenium-based complexes and organic dyes are commonty used. Natural
dyes extracted from plants can also be used as photo sensitiser.
Electrolyte: Redox couple iodide/triiodide solution is used as the electrolyte. Electrolyte
should have good contact with the dye-sensitized metal oxide semiconductor and the counter
electrode,
Counter electrode: Platinum or graphite-based materials are employed as the counter elec~
which acts as the cathode. It facilitates the reduction of the oxidized dye molecules and
he electrical circuit,
Schematic representation of DSSC employing titanium dioxide semiconductor and iodide/triiodide
electrolyte is given in fig. 2.11,
Nano TiO,
Ptlayer
Oye
Figure 2.11: Schematic representation of DSSC
(Source: [Link] 133512)
24.2. Working of Dye-sensitized solar cells
Sunlight passes through the transparent conductive oxide layer and the dye molecules coated
on the metal oxide semiconductor absorb the light. The electrons of the dye molecule then
get excited and are injected into the conduction band of the metal oxide semiconductor, These
electrons travel through metal oxide and move towards the external circuit to generate electric
current. Electrons reach the counter electrode through the circuit and generate electricity, The
oxidized dye molecules will get reduced by gaining electrons from the electrolyte and come
Chemistry for Information Science and Electrical Science (Common for Group A & B)" Chapter 2: Materials for
tronic Application
diffuse towards the counte
back to thew original form, The ovidized electrolyte spec!
Tele
trode and get reduced, s tw produce the current
Phis process continues
of DSSC
+ The fabrication of DSSCs is simpler processes compared fo conventional sHicon sola,
cells.
2.4.3 Advantag
1 can be advantageous for applications on vehicles and portate
* They are lightweight whi
devices,
They are flexible in shape, and size and hence can be implemented on windows, terraces,
facades, ete
+ Naturat pigments and organic dyes can be employed makes them more sust
ccottiendly and attordable
inable,
2.4.4 Applications of DSSC |
g
SSCs are mainly used for sunlight harvesting
* Since they can be used in window, facades ete... they can generate power while maintain
ing aesthetic appearance
+ They can be used in portable solar chargers for electronic de
and tablets due to its lightweight
es, such ay smartphones
+ They can be integrated into the fabric of bags and backpacks, enabling them to charge
electronic devices while on the go, This feature makes them particularly popular among
hikers and travellers who need a portable and convenient power source
+ DSSC can be used to power illuminated signs and displays in locations where acces
electricity is limited or costly
2.5 Spintronics
Spintronies or spin-electronics is an emerging field that exploits the spin of electrons, in
addition to charge. t process information in new generation transistors, lasers and integrated
magnetic sensors. They act by stonng information in elecuon spins, transmitting this infor- |
mation via mobile electrons and reading it at a terminal. Spin orientation lasts longer than
charge-based information, making them suitable for memory storage, magnetic sensors and
quantum computing.
Spintronics is basically connected to magnetism since the magnetic moment of electron is
proportional to its spin. Spintronics make use of the magnetoresistive effects for sensing and
storing information. The discovery of giant magnetoresistance (GMR) has a crucial role in the
development of spintronics. GMR is a phenomenon where a material's electrical resistance
changes dramatically when exposed to a magnetic field. This effect is widely used in magnetic
storage (eg. Magnetic random-access memory) and sensing technologies. Albert Fert and
Peter Grunberg, were awarded the Nobel Prize in Physics in 2007 for this ground breaking
Chemistry for Information Science and Electrical Science (Common for Group A & B)
eeChapter 2: Materials for Electronic Applications a
Snare ee suai
discovery. Giant magnetoresistive spin-valve sensor have improved the capacity of hard dise
rive by more than hundred-fold times. ‘This sensor comprises a metallic stack of ultra-thin
ferromagnetic layers separated by a thin copper layer.
A spin polarised current can be generated in a very simple way by passing the current through
a ferroelectric material. Spintronics materials should retain ferromagnetism practical temper
atures. There are metal based, semiconductor based and graphene based spintronics, Metal
oxides such as MgO, AlaOg, SrTiO, ete are examples of metal based spintronies materials.
Temary alloys such as InAs and GaAs alloyed with Mn, (Co, Fe, B). (Ga, Fe)N ete are used as
semiconductor based spintronic materials due to their tunable magnetic and proper
ties. Graphenes are also used for development of spintronics duc its efficient spin manipulat
properties.
jectroni
terials in Quantum Computing Technologies
6 Ma
Quantum computing is an emerging computer technology that uses the principle of qua
tum theory for computation. Quantum computers hamess the properties such as superposition
(quantum particles as combination of all possible states), entanglement (ability of quantum
particles to correlate their measurgment results with each other) and quantum interference (be~
haviour of a qubit, arising from superposition, which influences the probability of the qubit
collapsing to one state or another upon measurement) for computing,
In conventional computers using semiconductors, electrons represent binary states (0 or 1),
with eight bits covering numbers singly between 0 and 255. Quantum computing uses quan-
tum bits (qubits) that are superpositions of ‘spin up" and ‘spin down’ states, allowing them
{o represent all numbers between 0 and 255 simultancously. This allows quantum computers
to perform many calculations in parallel, Spintronic devices have the potential for quantum
computing. The spins of the electrons are expected to play an important role in the quantum
computers, as they can be used as qubits or quantum bit.
‘al boron nitride, a material consisting of just a few monolayers of atoms, can be
Hexagon:
acitors used in superconducting qubits. Di-
stacked to serve as the insulating layer in the
amonds with nitrogen-vacancy (NV) centers, nanowires, including semiconductor, supercon
ducting, and topological nanowires are also used in quantum computing. Metals ike Al, ND are
Used in used in superconducting circuits. Quantum dots materials like indium arsenide (InAs)
and gallium arsenide (GaAs) are employed to produce single photons, which are crucial for
quantum communication applications. Quantum computing requires very low temperatures to
avoid decoherance so that quibts remains in their quantum states and prevents error rates.
2.7. Supercapacitors
Supercapacitors or ultra capacitors are energy storage devices having high-capacity, with a
capacitance value much higher than solid-state capacitors but with lower voltage limits. Both
capacitors and batteries are energy storage devices. The differences between capacitors and
batteries are given in table 2.1.
Tn supercapacitors energy is stored electrostatically and electrochemically and bridges the gap
Chemistry for Information Science and Electrical Science (Common for Group A & B)n Chapter 2: Materials for Electronic Application,
ipacitors—_
Capacitor ii
Table 2.1; Differences bets
Battery =
Blectrical energy is stored in the fo
| chemi
ene!
|
|
ty is low ~ al
Cnty oncliy (release See
power density (release energy)
inergy density is very high
Lower power density (release
slowly)
acitors and batteries. A capacitor contains two metal plates separated
by a dielectric material whereas a super capacitor generally consists of electrodes, electrolyte,
separator and collector.
Electrode: Materials with good conductivity and high stability like porous active carbon
coming are generally used as the electrode material. Carbon based nanoparticles (eg. car.
bon nano tubes, graphene, carbon quantum dots etc.), metal oxide nanoparticles, nanowires,
quantum dots, conducting polymer-based composites etc. are used as the electrode material in
supercapacitors. Nanomaterials enhances the performance of the supercapacitors by increasing
the capacitance, energy density, and cycling stability of the supercapacitors
Electrolyte: Capacity of the capacitor depends mainly on the dielectric constant of the elec-
trolyte. Either solid or liquid can be used as the electrolyte. For commercial application solid
electrolytes are preferred since they are leak-free and possess high ionic conductivity. Gener-
ally, a solvent mixed with conductive salts such as tetraalkylammonium or lithium salts acts as
the solid electrolyte. Sulphuric acid, KOH solution etc can act as the liquid electrolyte.
Separator: Electrolyte membranes will act as the separator. It prevents short-circuiting be-
tween the electrodes but allows the electrolyte ions to pass through. Polymer-based and paper-
based are found to be durable and economical.
Collector: Electrons are collected at the collector. Carbon fibre, metal like Al, Pt, Cu, Ni ete.
are the commonly used collectors. Binders, such as polyvinylidene fluoride (PVDF) and poly-
acrylonitrile (PAN), act as adhesives to hold the active material and current collectors together.
Advantages of supercapacitor
+ Longer cycling time and higher service life compared to the battery.
* High efficiency, higher charging rates and high power density.
+ Low resistance which enables them to produce high load currents,
*+ Small sizes and lightweight which makes them easily installed in small
areas.
+ Environment friendly.
Chemistry for Information Science and Electrical Science (Com; for Group A & B)
mon for Group
eeChapter 2: Materials for Electronic Applications 73
pisadvantages of supereapacitor
+ Higher self discharge rate.
= Amount of energy stored per unit weight is considerably lower compared to batteries.
+ Low voltage limits which demand serial connections to produce high voltage.
Applications of supereapacitors
* Used in hybrid buses in combination with the battery to increase battery life and decrease
the size.
« Used in implantable devices and health monitoring devices to supply power.
«Used in solar-powered road and farming devices, street light portable traffic light system,
wireless security camera etc.
« Used in wind turbines to supply power to the pitch control of blade.
+ Memory devices in laptops, smartphones, tablets etc., are developed using supercapaci-
tors.
2.8 Questions
2.8.1 Short answer questions
1. "Properties of nanomaterial differ from bulk material” rationalize the statement with suit-
able example.
Write a note on sol-gel method of nanoparticle synthesis.
3, Give any three applications of nanomaterials.
4, List any three properties of graphene.
5. Explain the electrical conductivity of graphene based on its structure:
6. List any three applications of carbon nano tubes.
7. What are carbon quantum dots?
8. What are fullerenes?
9, Discuss the structure and bonding in Buckminster fullerene.
10. How halogenated polymers quench fire?
11, Name and write the structure of any two fire retardant polymers.
12, What are conducting polymers? Draw the structure of polyacetylene and polyaniline.
13. Explain doping in conducting polymers.
Chemistry for Information Science and Electrical Science (Common for Group A & B)for Electronic Applic
Chapter 2: Mi
140 Why conducting polymers like poly aniline and poly pyrrole ean be doped only wig, ,
type dopents’?
Show how polaron moves ina conducting polynt
What are polaran and bipoli
17, Write the synthesis of polypyrrote,
IS. Mention any thre Ds over LED and LCD. y
advantages of OL
ventional inorganic LEDs,
19, Why n region acts as emissive layer in contrast conv
red! solar cells,
20. Give any three advantages of dye sensi
21. What do you mean by spintronies.
22. List the materials used for quantum computing,
2.8.2 Es:
‘AY questions
js with example.
1. Discuss the classification of nanomate
2. Give the properties and application of nano mater
of nano
3, Explain the sol-gel method and chemical reduction methods for the synthesi
particles.
Discuss the synthesis, properties and application of graphene.
5. Explain the classification of carbon nano tubes.
and application of carbon nano tubes,
6, Describe the synthesis, propertic
7. Discuss the properties and application of carbon quantum dots.
Explain the structural features and applications of fullerenes.
sification of conducting polymet
9, Explain the e|
10. What is meant by doping of polymers? Deser
¢ the different types of doping.
11. How is polyaniline synthesized? List any two properties and applications.
12. How is polypyrrole synthesized? Li
any two properties and applications.
13, What are OLEDs? Explain the construction and working of OLED with the help of @
neat labelled sketch.
14, What are dye sensitized solar cel
the help of a neat labelled sketch,
Explain the construction and working of DSSC with
intronics
tive sl es on materials used for s :
15. Give short notes ¢ c ed for and quantum computing.
16, Mention the advantages, disidvantages and applications of super capacitors
rials used in supercapacitors,
plain the mi
stry for Information Science and Electrical Science (Common for Group A é eB)
af ion for