Winter semester 2023-2024

Engineering Chemistry (BCHY101L)

Module 4

Energy Devices

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 Contents…. (6 hours)
 Electrochemical and electrolytic cells
 Electrode materials with examples
• Semi-conductors
 Chemistry of Li ion secondary batteries
 Supercapacitors
 Fuel cells: H2-O2 and solid oxide fuel cell (SOFC)
 Solar cells: Photovoltaic cells (silicon based), Photoelectrochemical
cells, Dye- sensitized cells.

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 Electrochemical Cell
 A device that is used to generate electricity from a spontaneous redox reaction
or, conversely, that uses electricity to drive a non-spontaneous redox reaction.
 An electrochemical cell typically consists of
• Two electronic conductors (also called electrodes >> anode and cathode)
• An ionic conductor (called an electrolyte)
• the electron conductor used to link the electrodes is often a metal wire,
such as copper wiring
 The electrochemical cells are broadly classified into two types:
• Galvanic or voltaic cell: Converts the energy released by a spontaneous
chemical reaction to electrical energy. ΔG < 0
• Electrolytic cell: Consumes electrical energy from an external source to drive
a non-spontaneous chemical reaction. ΔG > 0
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 Galvanic or voltaic cell
 A galvanic cell uses the energy released during a spontaneous redox reaction
(ΔG < 0) to generate electricity.
 This type of electrochemical cell is also called a voltaic cell after its inventor, the
Italian physicist Alessandro Volta.
 Anode is written on the left-hand side >> oxidation occurs
 Cathode is written on the right-hand side >> reduction occurs
Electrode on the left Electrode on the right
Metal (or solid phase)| Electrolyte (whole Electrolyte (whole formula or ion) | Metal
formula or ion) (or solid phase)
Zn|Zn(NO3)2 (1M) Cu(NO3)2 (1M)|Cu
Oxidation: M1 → M1n+ + n e- Reduction: M2n+ + n e- → M2
Overall representation of Galvanic cell
M1 | M1n+ (C1) ║ M2n+ (C2) | M2 4
 Daniel Cell
 Invented by British chemist John Frederic
Daniell.
 Zn Electrode dipped in ZnSO4 solution:
• Oxidation: Zn → Zn2+ + 2 e-
 Cu Electrode dipped in CuSO4 solution:
• Reduction: Cu2+ + 2 e- → Cu
 Each electrode is referred to as half cell which
are connected through a salt bridge
 Salt bridge: KCl or NH4Cl in a gelatine form
 Maintains the charge balance in the two half
cells
 Minimizes or eliminates the liquid junction
potential 5
 EMF of Electrochemical Cell
 The electromotive force (EMF): Maximum potential difference between two electrodes of
a galvanic or voltaic cell.
 This quantity is related to the tendency for an element, a compound or an ion to acquire
(i.e. gain) or release (lose) electrons.
 Cell reaction is feasible when Ecell has positive value.
 Cell EMF in terms of Nernst Equation:
𝒏+ ሿ
𝟎. 𝟎𝟓𝟗 ሾ𝑴𝟏
𝑬𝒄𝒆𝒍𝒍 = 𝑬𝟎𝑴𝟏 − 𝑬𝟎𝑴𝟐 + 𝐥𝐨𝐠 𝟏𝟎 𝒏+
𝒏 ሾ𝑴𝟐 ሿ
𝑬𝟎𝑴𝟏 = 𝑺𝒕𝒂𝒏𝒅𝒂𝒓𝒅 𝒓𝒆𝒅𝒖𝒄𝒕𝒊𝒐𝒏 𝒑𝒐𝒕𝒆𝒏𝒕𝒊𝒂𝒍 𝒐𝒇 𝒄𝒂𝒕𝒉𝒐𝒅𝒆, 𝑴𝟏
𝑬𝟎𝑴𝟐 = 𝑺𝒕𝒂𝒏𝒅𝒂𝒓𝒅 𝒓𝒆𝒅𝒖𝒄𝒕𝒊𝒐𝒏 𝒑𝒐𝒕𝒆𝒏𝒕𝒊𝒂𝒍 𝒐𝒇 𝒄𝒂𝒕𝒉𝒐𝒅𝒆, 𝑴𝟐

 For equimolar solution of electrolytes corresponding to M1 and M2:

𝑬𝒄𝒆𝒍𝒍 = 𝑬𝟎𝑴𝟏 − 𝑬𝟎𝑴𝟐
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1. Write the half cell reaction, the net reaction and cell EMF of the following cell:
Cd|Cd2+ (0.01 M)║Cu2+ (0.5 M)|Cu
The standard reduction potentials are ̶ 0.40 V and 0.34 V respectively.

 The half reactions:

At anode: Cd → Cd2+ + 2 e- Standard reduction potential = ̶ 0.40 V
At cathode: Cu2+ + 2 e- → Cu Standard reduction potential = 0.34 V
 Net reaction: Cd + Cu2+ → Cu + Cd2+
 Cell EMF: 𝟎. 𝟎𝟓𝟗 ሾ𝟎. 𝟓ሿ
𝑬𝒄𝒆𝒍𝒍 = 𝟎. 𝟑𝟒 − (−𝟎. 𝟒𝟎) + 𝐥𝐨𝐠 𝟏𝟎
𝟐 ሾ𝟎. 𝟎𝟏ሿ
𝟎. 𝟎𝟓𝟗
= 𝟎. 𝟕𝟒 + 𝐥𝐨𝐠 𝟏𝟎 𝟓𝟎
𝟐
𝟎. 𝟎𝟓𝟗
= 𝟎. 𝟕𝟒 + × 𝟏. 𝟕
𝟐
= 𝟎. 𝟕𝟒 + 𝟎. 𝟎𝟓 = 𝟎. 𝟕𝟗 𝑽 7
 The Electrolysis of Molten NaCl
 Here Na+ ions gain electrons and are reduced
to Na at the cathode.
 As Na+ ions near the cathode are depleted,
additional Na+ ions migrate in.
 Similarly, there is net movement of Cl- ions to
the anode where they are oxidized to Cl2.
 Positive terminal is connected to the anode.
 The negative terminal is connected to the
cathode which forces electrons to move from
the anode to the cathode.
 Electrolysis is performed at ~ 801 °C.
 Here inert electrodes are used.

Cathode: 2 Na+ (l) + 2 e- → 2 Na (l)

Overall: 2 NaCl (l) → 2 Na (l) + Cl2 (g)
Anode: 2 Cl ̶ (l) → Cl2 (g) + 2 e- 8
 Electrolytic Decomposition of Water
 A pair of inert electrodes are dipped into the
solution and applying a voltage between
them results in the rapid evolution of bubbles
of H2 and O2.
 Due to very poor electrical conductivity of
pure water, a small amount of an ionic solute
(such as H2SO4 or Na2SO4) is added to increase
its electrical conductivity.
 The electrolytes are chosen such a way that
the ions that are harder to oxidize or reduce
than water:
Cathode: 4 H+(aq) + 4 e- → 2 H2(g)
Anode: 2 H2O → O2(g) + 4 H+ + 4 e-
Overall: 2 H2O → O2(g) + 2 H2(g)
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 Semiconductors
 A semiconductor is a substance, usually a solid chemical element or compound that
can conduct electricity under some conditions but not others, making it a good medium
for the control of electrical current.
 It has almost filled valence band, empty conduction band and very narrow energy gap i.e.,
of the order of 1 eV. Energy gap of Silicon (Si) and Germanium (Ge) are 1.0 and 0.7 eV
respectively. Consequently Si and Ge are semiconductors.

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 Effect of temperature on conductivity of semiconductors:
 At 0 K electrons freeze at valence band and hence all semiconductors are insulators.
 Electrical conductivity of a semiconductor material increases with increasing temperature
as resistivity decreases.
 At higher temperature transition from the valence band to the conduction band gets
facilitated  higher conductivity or lower resistivity.

Temperature
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Types of semiconductors:

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 Intrinsic Semiconductor
 Intrinsic semiconductor material is chemically very pure and possesses poor conductivity.
 It has equal numbers of negative carriers (electrons) and positive carriers (holes)

Absence of Presence of
electrical field electrical field

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 Extrinsic Semiconductor.
 Extrinsic semiconductor is an improved intrinsic semiconductor with a small amount
of impurities added by a process, known as doping, which alters the electrical
properties of the semiconductor and improves its conductivity.
 Introducing impurities into the semiconductor materials (doping process) can control
their conductivity.
 Doping process produces two groups of semiconductors:
• The negative charge conductor (n-type)
• the positive charge conductor (p-type)
 Semiconductors are available as either elements or compounds.
 Silicon and Germanium are the most common elemental semiconductors.
 Compound Semiconductors include InSb, InAs, GaP, GaSb, GaAs, SiC, and GaN.

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 n-type Semiconductor
 An n-type semiconductor is an intrinsic semiconductor doped with pentavalent
impurity, such as, P, As, Sb, etc.
 If a small amount of phosphorus is added to a pure silicon crystal, one of the
valence electrons of phosphorus becomes free to move around (free electron)
as a surplus electron.

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 p-type Semiconductor
 An p-type semiconductor is an intrinsic semiconductor doped with trivalent
impurity, such as, B, Al, In, etc.
 If a small amount of boron is doped to a single crystal of silicon, valence
electrons will be insufficient at one position to bond silicon and boron, resulting
in holes that lack electrons.

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 Preparation of Semiconductors:  99.9999% pure Si and Ge
 Distillation:
• Separation of materials is based on the difference in boiling points.
• For Ge  GeCl4 and for Si  SiHCl3
• As is removed from GeCl4 (b.p. 83.1 0 C) with the help of HCl.
• Pure GeCl4 is obtained by fractional distillation in presence of chlorine.
• After cooling, the pure GeCl4 is treated with extra pure water to get germanium
oxide.
• Subsequent reduction of GeCl4 with pure hydrogen affords highly pure elemental Ge.

GeCl4 + 2 H2O  GeO2 + 4 HCl

GeO2 + 2 H2  Ge + 2 H2O
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 Zone refining
 Difference between solubility of impurities in the molten and solid phases is used to
concentrate impurities at the end section of the ingots.
 The technique is based on the principle that when an impure metal in a molten state is
allowed to cool, only the metal crystallizes while the impurities remain present in
the molten state (mass) or melt.
 Used for the purification of germanium, silicon, gallium etc.

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 Czochralski crystal pulling technique
 Ge or Si obtained by zone refining method is polycrystalline, i.e., there is no regularity in
their crystal structure and contain crystals of different sizes.
 This method involves growing the crystal on a single crystal seed; thereby the atoms
reproduce identical atomic arrangement as that of the seed crystal.

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Silicon crystal with a
diameter of 300 mm and a
weight exceeding 250 kg

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 Doping techniques
 Epitaxy:
• Involves in unified crystal growth or deposition of a thin crystal on another substrate.
• Si or Ge wafer (kept in graphite boat) is placed in a long cylindrical quartz tube reactor,
which is then heated (by RF induction coil). Then gases containing compounds of Ge or
Si mixed with calculated/appropriate quantities of dopant over the wafer results.
• For getting Si epitaxial film, SiCl4, H2 and N2 mixture is used.
• For n-type doping  above mixture is used with phosphine (PH3)
• For p-type doping  Diborane (B2H6) is employed.
 Diffusion technique:
• Conversion of a region of semiconductor material by solid or gaseous diffusion of
impurity atom into the crystal lattice of the semiconductor material without any
melting and it consists of heating a P-type dopant.
• By this technique, the extent of impurity atoms penetration can be controlled
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even less than a few millions of a centimetre.
 Battery
 Battery is a device that consists of one or more electrochemical cells connected in series or
parallel or both and converts the chemical energy into electrical energy.
 The cell consists of three major components:
• The anode: Reducing electrode which gives up electrons to the external circuit
• The cathode: Oxidizing electrode which accepts electrons from the external circuit
• The electrolyte: It is the ionic conductor
 Types of Cells/Batteries:
• Primary battery (Primary cells): The cell reaction is not reversible. When all the reactants
have been converted to product, no more electricity is produced, and the battery is dead.
Example: Lechlanche Cell (Dry Cell), Alkaline Cell and Lithium batteries.
• Secondary battery (secondary cells): The cell reactions can be reversed by passing electric
current in the opposite direction. Example: Lead acid batteries, Ni-Cd batteries, Ni-Metal
Hydride batteries, Lithium ion batteries.
• Flow battery and fuel cell: Materials (reactants, products, electrolytes) pass through the
battery. Example: Hydrogen-oxygen fuel cell (HOFC), Solid oxide fuel cell(SOFC), etc. 22
 Lithium-Ion (Li ion) Batteries
 Lithium-ion battery is a secondary battery.
 It does not contain metallic lithium as anode.
 As the name suggests, the movement of lithium ions are responsible for charging &
discharging.
 Lithium ion battery technology was first proposed in the 1970s by M Whittingham who
used titanium sulphide for the cathode and lithium metal for the anode.
 The Nobel Prize in Chemistry 2019 is awarded to John B. Goodenough, M. Stanley
Whittingham and Akira Yoshino.

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 Why lithium?
 Currently, most portable electronic devices, including cell phones and laptop
computers, are powered by rechargeable lithium-ion (Li-ion) batteries, because:
 Lithium is a very light element.
 Li-ion batteries achieve a high specific energy density which is the amount of energy
stored per unit mass.
 Because Li+ has a very large negative standard reduction potential, Li-ion batteries
produce a higher voltage per cell than other batteries.
 A Li-ion battery produces a maximum voltage of 3.7 V per cell, nearly three times
higher than the 1.3 V per cell that nickel–cadmium and nickel–metal hydride
batteries generate.
 As a result, a Li-ion battery can deliver more power than other batteries of
comparable size, which leads to a higher volumetric energy density—the amount of
energy stored per unit volume.
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 Construction of Lithium-Ion (Li ion) Batteries
 Cathode: This is the positive electrode and it is
typically layers of lithium-metal oxide (LiCoO2,
LiNiO2, LiMn2O4, LiNiMnCoO2) and lithium metal
polyanionic materials (LiFePO4, LiMnPO4, LiFeSO4F,
etc.).
 Anode: The negative electrode is made from
graphite, usually with composition Li0.5C6.
 Electrolyte: Mixture of organic carbonates such as
ethylene carbonate, diethyl carbonate.
 Separator: Prevents touching two electrodes. This
absorbs the electrolyte, and enables the passage of
ions, but prevents the direct contact of the two
electrodes within the lithium in cell. Polyethylene
(PE), polypropylene (PP), and PE/PP separators
with pore sizes are used.
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Charging Reaction and Discharging

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 Charging Reaction and Discharging
Charging Reaction: Discharging Reaction:
 When the cell is being charged, cobalt  Li+ ions move out of the anode and
ions are oxidized and release migrate through the electrolyte
electrons. where they enter the spaces between
 Simultaneously Li+ ions migrate out of the cobalt oxide layers.
LiCoO2 and into the graphite.  Simultaneously electrons flow through
 Electrons flow from the positive the external circuit.
electrode to the negative electrode.  Electrons reduce cobalt at ions at the
 The electrons and Li+ ions combine at positive electrode to regenerate LiCoO2.
the negative electrode.
Anode: LiCoO2 → Li1-nCoO2 + n Li+ + n e- Anode: LinC6 → C6 + n e- + n Li+
Cathode: C6 + n e- + n Li+ → LinC6 Cathode: Li1-nCoO2 + n Li+ + n e- → LiCoO2

LiCoO2 + C6 → Li1-nCoO2 + LinC6 Li1-nCoO2 + C6Lin → LiCoO2 + C627

 Lithium ion battery variants
NAME CONSTITUENTS ABBREVIATION MAJOR APPLICATIONS
CHARACTERISTICS

Lithium Cobalt LiCoO LCO High capacity Cell phones, laptops,

2
cameras

Lithium Manganese LiMn O LMO Lower capacity Power tools, medical,

2 4
Oxide hobbyist

Lithium Iron LiFePO LFP Lower capacity Power tools, medical,

4
Phosphate hobbyist

Lithium Nickel LiNiMnCoO NMC Lower capacity Power tools, medical,

2
Manganese Cobalt hobbyist
Oxide
Lithium Nickel Cobalt LiNiCoAlO NCA Electric vehicles and
2
Aluminium Oxide grid storage

• Lithium polymer (Poly-Carbon monofluoride) batteries have an output of 2.8 V and

28
moderately high energy density.
 Lithium-ion battery applications
 Portable power packs: Li-ion batteries are lightweight and more compact than other battery
types, which makes them convenient to carry around within cell phones, laptops and other
portable personal electronic devices.
 Uninterruptible Power Supplies (UPSs): Li-ion batteries provide emergency back-up power
during power loss or fluctuation events to guarantee consistent power supply.
 Electric vehicles: As Li-ion batteries can store large amounts of energy and can be recharged
many times, they offer good charging capacity and long life spans which creates high
demand for Li-ion battery packs for electric, hybrid or plug-in hybrid electric vehicles.
 Marine vehicles: Li-ion batteries are emerging as an alternative to gasoline and lead-acid
batteries in powering work or tug boats and leisure craft like speed boats and yachts.
 Personal mobility: Lithium-ion batteries are used in wheelchairs, bikes, scooters and other
mobility aids for individuals with disability or mobility restrictions.
 Renewable energy storage: Li-ion batteries are also used for storing energy from solar
panels and wind turbines as they can be charged quickly. They are lighter, more compact
and can hold higher amounts of energy than lead-acid batteries. 29
 Advantages & Disadvantages of Lithium Ion Battery
 Advantages:
• High energy density: High energy density is one of the biggest advantages of lithium ion
battery technology. This higher power density offered by lithium ion batteries is a great
advantage for their use in electronic gadgets and electric vehicles.
• Low self-discharge: Lithium ion cells is that their rate of self-discharge is much lower than
that of other rechargeable cells such as Ni-Cad and NiMH forms.
• Low maintenance: Lithium ion batteries do not require active maintenance.
• High cell voltage: The voltage produced by each lithium ion cell is about 3.6 volts. This
ensure less number of cells in many battery applications.
• Variety of types available: There are several types of lithium ion cell available. This ensures
the right technology can be used for the particular application needed.
• No requirement for priming: Lithium ion batteries are supplied operational and ready to
go.
• Load characteristics: These provide a reasonably constant 3.6 volts per cell before falling
30 off
 Disadvantages:
• Protection required: Lithium ion cells and batteries are not as robust as some other
rechargeable technologies. They require protection from being over charged and
discharged too far.
• Ageing: Lithium ion batteries suffer from ageing. Often batteries will only be able to
withstand 500-1000 charge discharge cycles before their capacity falls.
• High Cost: A major lithium ion battery disadvantage is their cost. Typically they are around
40% more costly to manufacture than Nickel cadmium cells.
• Chances of explosion:
• Bad design or manufacturing defects: In that case, there wasn’t enough space for the
electrodes and separator in the battery. When the battery expanded a little as it charged,
the electrodes bent and caused a short circuit.
• Overcharging: When overcharged, lithium cobalt oxide releases oxygen which can react
with flammable electrolyte leading to overheating.
• Electrolyte breakdown: On overheating, Dimethyl carbonate decompose to form CO2
which causes pressure build up in battery, resulting in a dangerous explosion. 31
 Batteries Vs Capacitors
 Batteries and capacitors do a similar job—storing electricity—but in completely different
ways. Batteries have two electrical terminals (electrodes) separated by a chemical
substance called an electrolyte.
 When power is on, chemical reactions happen involving both the electrodes and the
electrolyte. These reactions convert the chemicals inside the battery into other
substances, releasing electrical energy as they go. Once the chemicals have all been
depleted, the reactions stop and the battery is flat.

 A supercapacitor is a type of capacitor

that can store a large amount of
energy, typically 10 to 100 times more
energy per unit mass or volume
compared to electrolytic capacitors.
 These can deliver and accept charge Supercapacitors/
more quickly than batteries.
Ultracapacitors 32
 Capacitors
 A capacitor is a device used to store electrical charge
and electrical energy.
 Capacitors use static electricity (electrostatics)
rather than chemical substances to store energy.
 Inside a capacitor, there are two conducting metal
plates with an insulating material called a dielectric in
between them - it's a dielectric sandwich.
 Positive and negative electrical charges build up on
the plates and the separation between them, which
prevents them coming into contact, is what stores the
energy.
 The dielectric allows a capacitor of a certain size to
store more charge at the same voltage, so it makes
the capacitor more efficient as a charge-storing
device. 33
 A supercapacitor differs from an ordinary capacitor in two important ways:
• Its plates effectively have a much bigger area and the distance between them is much
smaller, because the separator between them works in a different way to a
conventional dielectric.
• Although the words "supercapacitor” and "ultra capacitor” are often used
interchangeably, there is a difference: they are usually built from different materials
and structured in slightly different ways, so they store different amounts of energy.
 Like an ordinary capacitor, a supercapacitor has
two plates that are separated.
 The plates are made from metal coated with a
porous substance such as powdery, activated
charcoal, which effectively gives them a bigger
area for storing much more charge. Unlike
capacitor, in a supercapacitor, there is no dielectric
as such. Instead, both plates are soaked in an
electrolyte and separated by a very thin insulator
(which might be made of carbon, paper, or plastic) 34
 How do Supercapacitors Work?
 When the plates are charged up, an opposite charge forms on either side of the separator,
creating what's called an electric double-layer.
 This is why supercapacitors are often referred to as double-layer capacitors, also called
electric double-layer capacitors or EDLCs).
 The capacitance of a capacitor increases as the area of the plates increases and as the
distance between the plates decreases.

35
 Application of Supercapacitors
 Supercapacitors have been widely used as the electrical equivalents of flywheels in
machines—"energy reservoirs" that smooth out power supplies to electrical and
electronic equipment.
 Supercapacitors can also be connected to batteries to regulate the power they supply.
 In wind turbines, where very large supercapacitors help to smooth out the intermittent
power supplied by the wind. In electric and hybrid vehicles, supercapacitors are
increasingly being used as temporary energy stores for regenerative braking (where the
energy a vehicle would normally waste when it comes to a stop is briefly stored and then
reused when it starts moving again).

36
 Fuel Cells
 A fuel cell is a device that converts chemical potential energy (energy stored in molecular
bonds) into electrical energy without combustion.
 They offer higher electrical efficiency (≥ 40%) compared to conventional power
generation systems.

37
 Principle of Operation
 A fuel cell is a device that uses hydrogen (or hydrogen-rich fuel) and oxygen to
create electricity by an electrochemical process.
 Hydrogen and oxygen (air) are supplied to anode and cathode, respectively.
 When hydrogen is led to the anode, the hydrogen molecules are split into
proton and an electron. The protons migrate through the electrolyte to the
cathode, where they react with oxygen to form water.
 At the same time, the electrons are forced to travel around the electrolyte to
the cathode side, because they cannot pass through the electrolyte. This
movement of electrons thus creates an electrical current.

38
 Types of Fuel Cells
 There are eight main types of fuel cells, based mainly on the type of electrolyte:
• PEMFCs, proton exchange membrane or polymer electrolyte membrane fuel
cells
• AFCs, alkaline fuel cells
• PAFCs, phosphoric acid fuel cells
• MCFCs, molten carbonate fuel cells
• SOFCs, solid oxide fuel cells
• DMFCs, direct methanol fuel cells
• DAFCs, direct ammonia fuel cells
• DCFCs, direct carbon fuel cells
 Apart from DAFCs, DMFCs, and DCFCs, other types of fuel cells are fed with
hydrogen. 39
 Hydrogen – oxygen fuel cells (HOFC)
 This cell is a common type of fuel cell. Similar to a galvanic cell, fuel cells also
have two half cells.
 Both half cells have porous graphite electrode with a catalyst (platinum, silver
or a metal oxide).
 The electrodes are placed in the aqueous solution of NaOH or KOH (alkaline
fuel cells-AFC) or H2SO4 (acidic fuel cell) which acts as an electrolyte.
 Hydrogen and oxygen are supplied at anode and cathode respectively at about
50 atmospheric pressure, the gases diffuse at respective electrodes.
 The overall chemical reaction in a hydrogen fuel electrochemical cell involves
the oxidation of hydrogen by oxygen to produce only water.
2 H 2 + O 2 → 2 H 2O 40
 Proton exchange membrane fuel cell (PEMFC)
or
Polymer electrolyte membrane fuel cells (PEMFC)
 This type of fuel cell utilize water-based, acidic polymer electrolyte
membranes (PEMs), such as Nafion, to conduct protons for ion exchange
purposes.
 PEMFC cells operate at relatively low temperatures (< 80°C).
 Due to the relatively low temperatures and the use of precious metal-based
electrodes, these cells must be operated on pure hydrogen.

Nafion
41
 Process
 Hydrogen fuel is processed at the anode where electrons are separated from
protons on the surface of a platinum-based catalyst.
 The protons pass through the membrane to the cathode side of the cell while
the electrons travel in an external circuit, generating the electrical output of the
cell.
 On the cathode side, another Pt electrode combines the protons and electrons
with oxygen to produce water.

• At anode: H2 (g) → 2 H+ + 2 e-
• At cathode: O2 (g) + 4 H+ + 4 e- → 2 H2O
• Net reaction: O2 (g) + 2 H2 (g) → 2 H2O (I)
ECell˚= 1.23 V
42
PEMFC

43
 Advantages
• The energy conversion is very high (75-82%).
• Fuel cell minimizes expensive transmission lines and transmission losses.
• It has high reliability in electricity generation and the by-products are environmentally
acceptable.
• Maintenance cost is low for these fuels and they save fossil fuels.
• Noise and thermal pollution are very low.
 Disadvantages:
• The major disadvantage of the fuel cell is the high cost and the problems of durability and
storage of large amount of hydrogen.
• The accurate life time is also not known and It cannot store electricity.
• Electrodes are expensive and short lived.
• Storage and handling of H2 gas is dangerous because it is inflammable.

 Applications:
• The most important application of a fuel cell is its use in space vehicles, submarine or military
vehicles.
• The product H2O is valuable source of fresh water for the astronauts.
• Fuel cell batteries for automotive will be a great boon for the future. 44
 Solid Oxide Fuel Cell (SOFC)
 SOFC is a high-temperature FC that utilizes solid ceramic inorganic oxide as an
electrolyte; e.g., zirconium oxide stabilized with yttrium oxide, instead of a
liquid or membrane, also known as Yttria-stabilized Zirconia (YSZ).
 SOFC is also referred to as ceramic FC.
 Both hydrogen and carbon monoxide are used as fuels.
 Solid oxide fuel cells work at very high temperatures, the highest of all the fuel
cell types at around 800 °C to 1,000 °C.
 Efficiency: over 60% when converting fuel to electricity
 This cell is relatively resistant to small quantities of sulphur in the fuel,
compared to other types of fuel cell, and hence can be used with coal gas.
45
 Structure of SOFC
 Anode or fuel electrode:
• Nickel mixed with YSZ (Yttria stabilized Zirconia) or called Nickel-YSZ cermet (a cermet
is a mixture of ceramic and metal).
• It is a porous ceramic layer to allow the fuel to flow towards electrolyte.
 Cathode or air electrode:
• The cathode is usually a mixed ion-conducting and electronically conducting ceramic
material.
• It is a thin porous ceramic layer coated over the solid electrolyte where oxygen
reduction takes place. One example being, strontium doped lanthanum manganite
(LSM).
 Electrolyte:
• Oxide ion (O2-) conducting ceramic.
• The most popular electrolyte material is a bilayer composite electrolyte (YSZ layer +
gadolinium doped CeO2) (GDC) layer) or a mixture of ZrO and CaO.
46
 At anode (oxidation):
H2 (g) + CO (g) + 2 O2- → H2O (g) + CO2 (g) + 4e-
 At cathode (reduction):
O2 (g) + 4e- → 2 O2-
 Net reaction:
H2 (g) + CO (g) + O2 (g) → H2O (g) + CO2 (g) 47
 Advantages of SOFC:
• SOFCs have a number of advantages due to their solid materials and high
operating temperature.
• Since all the components are solid, as a result, there is no need for electrolyte
loss maintenance and electrode corrosion is eliminated.
• Also because of high-temperature operation, the SOFC has a better ability to
tolerate the presence of impurities as a result of life increasing.
• High efficiencies: Due to high-quality waste heat for cogeneration
applications and low activation losses, the efficiency for electricity
production is great.
• Low emissions. Releasing negligible pollution. It is the cleanest among all fuel
cells.
48
 Disadvantages:
• High operating temperature (500 to 1,000 °C) which results in longer start up
times and mechanical/chemical compatibility issues.
• The cost and complex fabrication are also significant problems that need to be
solved.

• Applications:
• SOFCs are being considered for a wide range of applications, such as working
as power systems for trains, ships and vehicles; supplying electrical power for
residential or industrial utility.
• Stationary power generation
• By product gases are channeled to turbines to generate more electricity:
cogeneration of heat and power and improves overall efficiency.
• Auxiliary power units in vehicles 49
Differences between Primary, Secondary and Fuel cells

50
 Solar Energy Potential
 Theoretical: 1.2x105 TW solar energy potential
(1.76 x105 TW striking Earth; 0.30 Global mean albedo)
Energy in 1 hr of sunlight ↔ 14 TW for a year
 Practical: ≈ 600 TW solar energy potential (50 TW - 1500 TW depending on land fraction
etc.; WEA 2000)
Onshore electricity generation potential of ≈ 60 TW (10% conversion efficiency)
Photosynthesis: 90 TW

51
Solar energy conversion devices

52
Types of solar energy conversion cells

• Photovoltaic Cells
• Photoelectrochemical cells
• Dye-sensitized solar cells

53
 Photovoltaic Cells
 A solar cell is a device that converts the energy of sunlight directly into electricity
by the photovoltaic effect.
 The photovoltaic effect involves creation of a voltage (or a corresponding electric
current) in a material upon exposure to electro-magnetic radiation.
 Though the photovoltaic effect is directly related to the photoelectric effect, the
two processes are different.
 There are several different types of PV cells which all use semiconductors to
interact with incoming photons from the Sun in order to generate an electric
current.
 Highly purified silicon (Si) from sand, quartz, etc. is “doped” with intentional
impurities at controlled concentrations often used in Photovoltaic Cells.
54
 Why Silicon?

Silicon is considered as the most suitable material for solar energy conversion because:
 Second most abundant element (~ 28% by mass) after oxygen
 Highly pure silicon can be readily synthesized from sand or quartz by heating them
at high temperature in furnace

SiO2 + C → Si + CO 2

 Silicon is an excellent semiconductor with optimum band gap of 1.23 eV at 300 K

 Cost effectiveness
 Silicon can be easily doped with phosphorus (P), arsenic (As), antimony (Sb), boron
(B), indium (In) or aluminium (Al).
55
 Types PV based on the structure of silicon: Crystal structure, or atomic
arrangement in a material plays crucial role in its electrical properties.
• Single-crystal silicon:
• In its crystalline form, a material is characterized by an ordered array of
component atoms. This array is repetitive with displacement through the
material sample.
• 15–18% efficient, typically expensive to make (grown as big crystal)

56
• Poly-crystalline silicon:
• Where a polycrystalline material is concerned, the object is composed of a
number of sub-sections, each of which is crystalline in form. These
subsections, however, are independently oriented so that at their interfaces
the atomic order and regularity undergo sharp discontinuities.
• 12–16% efficient, slowly improving and cheaper to make (cast in ingots)

57
• Amorphous silicon (non-crystalline)
• The final category, the amorphous material, displays no atomic regularity of
arrangement on any macroscopic scale.
• 4–8% Efficient and cheapest per Watt
• Called as “thin film” and easily deposited on a wide range of surface types

58
p-n junction

59
•System converts light energy to electricity

•Applications in Aerospace & Satellite etc 60

61
 Disadvantages of Photovoltaic Solar Cells
 Some toxic chemicals, like cadmium and arsenic, are used in the PV production
process. These environmental impacts are minor and can be easily controlled
through recycling and proper disposal.
 The conversion of light energy into heat energy is one of the limitations.
 Solar energy is somewhat more expensive to produce than conventional
sources of energy due in part to the cost of manufacturing PV devices
 Solar power is a variable energy source, with energy production dependent on
the sun.
 Solar panels efficiency levels are relatively low (between 14%-25%) compared to
the efficiency levels of other renewable energy systems.
 Solar panels are fragile and can be damaged relatively easily.
62
 Photoelectrochemical cells

 Photoelectrochemical cell is a photocurrent generated device

which is made up of an electrolyte and a photoactive
semiconductor electrode.
 Photoelectrochemical (PEC) cell is a device in which a photoactive
semiconductor material is in contact with an electrolyte .
 Irradiation of the SC/electrolyte junction with light of energy > Eg,
the band gap of the semiconductor, produces electron - hole pairs.
 The electron-hole pairs are spatially separated (due to the junction
potential) to drive oxidation and reduction reactions in the system.

63
 Photoelectrochemical cells
 Types of Photoelectrochemical cells:
• Liquid Junction Solar Cell (LJSC) – n-SC/Electrolyte/Metal
• The free e-s in SC absorb the high energy radiation and then the excited e-s
will move from the valance band to conduction band of the SC. As a result of
this, the holes (+) are created.
This cell is used to convert solar energy into electrical energy.
• Photoelectrosynthesis (PES) cells –
In this class of cells, solar energy is converted into chemical energy in the form
of fuels.

64
Regenerative photoelectrochemical cells

65
 Major advantages of PEC cells over photovoltaic cells

 Easy junction formation (mere dipping of the SC electrode in the

electrolyte).
 In-situ water electrolysis is possible.
 Efficiencies of polycrystalline bulk and thin film electrodes are
comparable to those of single crystal electrodes.
 Novel reaction products are possible and catalytic effects
(Photocatalysis) can be induced on the SC surfaces.
 Particulate systems can be used.

66
 Conditions for Efficient Solar Energy Conversion –
Electrodes

 The requirements for the electrode materials are:

(1) Band gap (Eg) should be optimum

(2) The doping level should be optimum, so that there will be a good spatial
separation of the photo-generated carriers and hence, high quantum
efficiency.
(3) Should have large values of absorption co-efficient (α). This is usually found
for direct band gap SC’s.
(4) Applied bias (external energy source) makes the LJSCs more efficient.

67
Working of PEC cells

68
 Dye Sensitization - Grätzel cell
1. Sunlight energy (photon of light) passes through the titanium dioxide layer and strikes
electrons within the adsorbed dye molecules. Electrons gain this energy and become
excited because they have the extra energy.
2. The excited electrons escape the dye molecules and become free electrons. These free
electrons move through the titanium dioxide and accumulate at the -ve plate (dyed TiO 2
plate).
3. The free electrons then start to flow through the external circuit to produce an electric
current. This electric current powers the light bulb.
4. To complete the circuit, the dye is regenerated. The dye regains its lost electrons from the
iodide electrolyte. Iodide (I-) ions are oxidised (loss of 2 electrons) to tri-iodide (I3-). The
free electrons on the graphite plate then reduce the tri-iodide molecules back to their
iodide state. The dye molecules are then ready for the next excitation/oxid/red cycle.
69
70
 Transparent and Conductive Substrate
• Substrate for the deposition of the semiconductor and catalyst, acting also as
current collectors
• Characteristics of a substrate:
More than 80% of transparency
Should have a high electrical conductivity.
• The fluorine-doped tin oxide (FTO, SnO2: F) and indium-doped tin oxide (ITO,
In2O3: Sn) are usually applied as a conductive substrate in DSSCs.
• These substrates consist of soda lime glass coated with the layers of ITO and
FTO.
• The ITO films have a transmittance > 80% and 18 Ω /cm2 of sheet resistance,
• FTO films show a lower transmittance of ~ 75% in the visible region and sheet
resistance of 8.5 Ω /cm2
71
 Working Electrode (WE)
• Working electrodes (WE) are prepared by depositing a thin layer of oxide
semiconducting materials such as TiO2, Nb2O5, ZnO, SnO2 (n-type), and NiO (p-
type) on a transparent conducting glass plate made of FTO or ITO
• These oxides have a wide energy band gap of 3 – 3.2 eV
• Due to its non-toxicity, and easy availability, TiO2 is mostly used as a
semiconducting layer
• To enhance its activity the TiO2 semiconducting layers are immersed in a
mixture of a photosensitive molecular sensitizer and a solvent
• Due to highly porous structure and the large surface area of the electrode, a
high number of dye molecules get attached on the nanocrystalline TiO2
surface, and thus, light absorption at the semiconductor surface increases.

72
 Photosensitizer or Dye
• Dye are responsible for the maximum absorption of light.
• These should have the following photophysical and electrochemical properties:
• Dyes should be luminescent.
• Their absorption spectra should cover UV-vis and NIR regions.
• The periphery of the dye should be hydrophobic to enhance the long-term stability of
cells.
• Co-absorbents like chenodeoxycholic acid (CDCA) or anchoring groups like alkoxy-silyl,
phosphoric acid, and -COOH should be present to avoid the aggregation of the dye
over the TiO2 surface.

73
 Electrolyte
• An electrolyte, such as I−/I3−, Br−/Br2−, SCN−/SCN2, and Co(II)/Co(III) has five main
components, i.e., redox couple, solvent, additives, ionic liquids, and cations.
• The following properties should be present in an electrolyte: :
• Redox couple should be able to regenerate the oxidized dye efficiently.
• Should have chemical, thermal, and electrochemical stability.
• Should be non-corrosive with DSSC components.
• Should be able to permit fast diffusion of charge carriers, enhance
conductivity, and create effective contact between the working and counter
electrodes.

 Counter Electrode (CE)

• CE in DSSCs are mostly prepared by using Pt, C, CoS, Au/GNP, alloy CEs like
FeSe, and CoNi0.25. 74
Photosensitizers or Dyes

75
Naturally Occurring Dyes

76
 Construction of a Grätzel cell
o In Grätzel cell a range of organic dyes are used.
o Examples: Ruthenium-Polypyridine, Indoline dye & metal free organic dye.
o These dyes are extractable from simple foods such as hibiscus tea, tinned summer fruits,
blackberries.

Construction:
o Two transparent glass plates are perforated on one side with a transparent thin layer of a
conducting material.
o Onto the conducting sides, one plate is coated with graphite and the other plate is coated with
titanium dioxide (TiO2).
o A dye is then adsorbed onto the TiO2 layer by immersing the plate into a dye solution of 10-4M in
alcohol for 10 min. (approx.)
o The plates are then carefully sandwiched together and secured using a paper clip.
o To complete the cell a drop of iodide electrolyte is added between the plates.
o Figure shows a Grätzel cell prepared from hibiscus tea.
o The upper plate is the TiO2 plate, dyed with hibiscus tea and the lower plate is coated with
graphite. 77
 Construction of a Grätzel cell
 In Grätzel cell a range of organic dyes are used.
Examples: Ruthenium-Polypyridine, Indoline dye & metal free organic dye.
 These dyes are extractable from simple foods such as hibiscus tea, tinned
summer fruits, blackberries.

Upper Plate :
Dye coated TiO2
Plate (Anode)

Lower Plate :
Graphite coated
conductor (Cathode)
78
 Working Principle
The working principle of DSSC involves four basic steps: light absorption, electron injection,
transportation of carrier, and collection of current.

 Sunlight energy (photon of light) passes through the titanium dioxide layer and absorbed
by the photosensitizer
 Due to the photon absorption, electrons get promoted from the ground state (Dye) to
the excited state (Dye*) of the dye
 Excited electrons with a lifetime of nanosecond range are injected into the conduction
band of nano-porous TiO2 electrode which lies below the excited state of the dye.
 As a result, the dye gets oxidized.

Dyeo + hν → Dye*

Dye* → Dye*+ + e- (TiO2)

79
Advantages and disadvantages of DSSC

80