ELECTROCHEMISTRY

Introduction, Single electrode potential, Origin of single electrode potential theory, Nernst
equation to calculate the electrode potential, Numerical problems. Electrochemical cells -
galvanic cell and electrolytic cell, representation of galvanic cell, Construction and working
of galvanic cell, Liquid junction potential, Functions of salt bridge, EMF of cell,
Determination of EMF of cell by Poggendroff’s method using Standard cell, Construction,
working, application and limitations of calomel electrode, Numerical problems. Construction,
working, applications, advantages and limitations of glass electrode, Numerical problems.
Classification of Batteries – Introduction, primary and secondary with examples;
construction, working and applications of lead acid battery. Construction, working and
applications of Ni-Cd and Li-ion batteries, advantages and disadvantages. Fuel Cells –
Introduction, construction and working of AFC & PEMFC, advantages and disadvantages.
Metal finishing – Electroplating – polarization, over voltage, decomposition potential
including determination of decomposition potential. Characteristics of good deposit, Factors
influencing the nature of the deposit, Methods of cleaning the metal surface. Electroplating of
Cu & Cr & electroless plating of Cu.

1 INTRODUCTION
Electrochemistry deals with the behavior of electrolytes in solution and inter
conversion of chemical and electrical energies; that is, the study of chemical changes due to
the flow of an electric current and production of electric current due to chemical reaction.
Electrolysis, electrometallurgy and electroplating use electrical energy to drive chemical
reactions, while chemical energy is transformed into electricity in galvanic cells, batteries and
fuel cells. Substances such as metals and alloys conduct electricity under the influence of an
applied electric potential through a flow of electrons and hence are known as electronic
conductors. The flow of electricity in electronic conductors does not cause any physical or
chemical change in the conductor. On the other hand electrolyte solutions and molten salts
conduct electricity through the migration of ions and are known as electrolytic conductors or
electrolytes. When direct current is passed through an electrolyte solution, decomposition and
changes occur in the composition of the electrolyte. The practical importance of
electrochemistry includes electroplating, electroextraction of metals, electrorefining of
metals, and electro-production of certain compounds.

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1.1 ELECTROCHEMICAL CELLS
An electrochemical cell consists of two electrodes or metallic conductors, in contact
with an electrolyte, an ionic conductor. An electrode and its electrolyte comprise an electrode
compartment. The two electrodes may share the same compartment. If the electrolytes are
different, the two compartments may be joined by a salt bridge, which is a tube containing a
concentrated electrolyte solution in agar jelly that completes the electrical circuits and
enables the cell to function. So an electrochemical cell can be defined as a single
arrangement of two electrodes in one or two electrolytes which converts chemical energy
into electrical energy or electrical energy into chemical energy. Electrochemical cells can
be classified into two types:
• Galvanic Cells
• Electrolytic Cells

external circuit

internal circuit

Fig.1.1. A schematic diagram of Electrochemical Cell

1.1.1 Galvanic Cells
A galvanic cell is an electrochemical cell that produces electricity as a result of the
spontaneous redox reaction occurring inside it. Galvanic cell generally consists of two
electrodes dipped in two electrolyte solutions which are separated by a porous diaphragm or
connected through a salt bridge. It is a single arrangement of two electrodes in one or two
electrolytes which converts stored up chemical energy in the form of electroactive materials
(anode & cathode active materials) directly into electrical energy. The negatively charged
electrons flow from anode to cathode and are attracted to the positive cathode through the
external circuit.

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Anode vs. Cathode:
Anode ;
• the electrode at which oxidation occurs
• is where electrons are produced
• is what anions migrate towards
• has a –ve sign.
Cathode ;
• the electrode at which reduction occurs
• is where electrons are consumed
• is what cations migrate towards
• has a –ve sign
A typical galvanic cell can be illustrated by Daniel cell (Fig. 1.1.1)

-
e
v

Oxidation at Zn reduction at Cu

Half cell(Anode compartment) Half cell(Cathode

compartment)

Fig.1.1.1. A schematic diagram of Daniel cell

A Daniel cell consists of two compartments, one of which contains zinc rod dipped in
zinc sulphate solution and the other with a copper rod dipped in a copper sulphate solution.
The two electrolytes are connected by a salt bridge. When the zinc and copper rod electrodes

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are connected externally through a voltmeter by using a wire, the following oxidation-
reduction reactions taking place at the electrodes. At the zinc electrode, zinc goes into the
solution as Zn2+ ions, liberating two electrons. In the process zinc undergoes oxidation
liberating two electrons. The positive ion flows from the salt bridge to the cathode and the
zinc electrode becomes lighter.
⚫ Zn (s) → Zn2+ (aq) + 2e- ---------------------------(1).
At the copper electrode reduction of Cu2+ ions takes place with the deposition of metallic
copper on the copper rod, by consuming two electrons. The negative ions flow from salt
bridge to anode and copper electrode becomes heavier. The ionic conduction in the solution
is coupled to the electronic conduction in the electrodes.
⚫ Cu2+ (aq) + 2e- → Cu(s) --------------------------- (2)
Each of these reactions is known as half cell reaction. The reaction (1) in which loss of
electrons takes place is called oxidation half reaction; while the reaction 2, in which gain of
electrons takes place, is called reduction half reaction. The net reaction is obtained by adding
reactions 1 and 2. i.e. Zn(s)+ Cu2+ (aq) → Zn2+ (aq) + Cu(s) is called redox or oxidation –
reduction reaction. When the circuit is closed, the electrons flow from zinc to copper through
the external wire to feed the Cu2+ ions in the process of discharging copper and thus electrical
energy or current is produced which may be used for the purpose of external work.
As in the case of Daniel cell, by the combination of any two different electrodes materials one
can construct a galvanic cell. The electrode with a greater tendency to go into the solution by
liberating electrons acts as an anode, & the other one with more tendency to undergo
reduction acts as a cathode. In a galvanic cell anode is negative and the cathode is positive.
The reason to this nomenclature is that oxidation is accompanied by the liberation of
electrons which are given up to that electrode which thereby acquires a negative charge.
Reduction on the other hand, is accompanied by absorption of electrons by reactant in
solution from the electrode, which thereby acquires a positive charge. Hence the flow of
electrons is from the negative electrode to positive electrode and the direction of flow of
positive electricity, which is known as conventional current, is from the cathode to anode.
1.1.2 Electrolytic cells
An electrolytic cell is an electro –chemical cell in which a non- spontaneous reaction is
driven by an external source of current although the cathode is still the site of reduction, it is
now the negative electrode whereas the anode, the site of oxidation is positive.
The electrolytic cell (Fig.1.1.2) find wide applications in the purification of metals & also in
electro deposition of a metal on to the surface of another metal, alloy or any conductor in
general, by the process of electrolysis.

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 CuSO 4 solution

SO42- Cu2+
Fig.1.1.2 Schematic diagram of an electrolytic cell
Electrolysis involves the conversion of electrical energy into chemical energy i.e. chemical
changes are brought about by the expense of electrical energy. Since electrolysis is a non
spontaneous process, the minimum energy required to carry out such a process is equal to the
free energy increase accompanying the change, & this is equal but opposite in sign to the free
energy decrease accompanying the reverse spontaneous process. This is true when
electrolysis is carried out reversibly. However, in irreversible conditions, the potential to be
applied for electrolysis is higher than the reversible emf of the cell.
1.1.3 Representation of a galvanic cell
According to the present convention, a galvanic cell is represented by keeping in view the
following points:
1. The anode is written on the left hand side and the cathode is written on the right hand
side of cell representation.
2. The anode is written by writing the metal (or solid phase) first and then the electrolyte
along with the concentration in the bracket. The two are separated by a vertical line or
a semicolon. The electrolyte may be represented by the formula of the whole
compound or by ionic species.
Anode representation
Metal/ Metal ion (concentration) i.e. M/Mn+ (c)
Zn│Zn2+ or Zn; Zn2+ or Zn │ ZnSO 4 (1M) or Zn; ZnSO 4 (1M)

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 3. The cathode of the cell is represented by metal ion first and then the metal (or solid
phase) thereafter. The two are separated by a vertical line or a semicolon.
Cathode representation:
Mn+ (c) / M i.e. Metal ion (concentration) / Metal
e.g. Cu2+│Cu or Cu2+; Cu or Cu2+ (1M); Cu or CuSO 4 (1M)/Cu
4. A salt bridge is indicated by two vertical lines, separating the two half-cells. Thus the
Daniel cell, may be represented as:
Zn │ ZnSO 4 (1M)║ CuSO 4 (1M)/Cu
Cu(s) / Cu2+ (aq) ║Ag+(aq) / Ag (s)
Comparisons of Galvanic and Electrolytic cells
Galvanic Cell Electrolytic Cell

1. Cell reaction is spontaneous 1. Cell reaction is non-spontaneous

2. Converts chemical energy to electrical
2. Converts electrical energy into chemical
energy energy
Anode is negative and cathode is positive 3. Anode is positive and cathode is negative
3. Usually have two electrodes and two
4. Single electrolyte and two electrodes
electrolytes
4. Used as a potable source of electrical
5.
energy in cars, flashlights and calculators Used for electrolysis apparatus like
Example. Daniel cell electroplating and electrorefining

Example. Electroplating of nickel

1.1.4 LIQUID JUNCTION POTENTIAL

The potential set up at the junction of the two electrolytes because of the difference in the
speeds of the cations in one direction and anions in the other i.e. potential at the junction of
the two electrolytes because of unequal migration of ions across the boundary between the
two solutions is called the liquid junction potential, E j. In a Daniel cell, if the concentrations
of ZnSO 4 (aq) and CuSO4 (aq) are equal SO4 2- ions do not diffuse across the junction and the
charge cannot flow around the circuit. But Cu2+ ions diffuse into ZnSO4 (aq) and Zn2+ ions
diffuse into CuSO4 (aq) because Cu2+ ions are slightly more mobile than Zn 2+ ions. This
produces a small excess positive charge on the ZnSO 4 (aq) side of the junction and equal

6
negative charge on the CuSO 4 (aq) side. The liquid junction potential is the difference
between the electric potential developed in the two solutions across their interface
i.e. Ej = Ø soln, R - Ø soln,L where Ø soln. R is the electric potential of the electrolyte solution on
the right hand side half – cell in the cell scheme. Ø soln. L is the electric potential of the
electrolyte solution on the left hand side half-cell. Generally, LJPs are of the order of a few
millivolts.
1.1.5 SALT BRIDGE
The contribution of the liquid junction to the potential can be reduced (to about 1 to 2
mV) by joining the electrolyte compartments through a salt bridge containing salts such as
KCl, KNO 3 , and NH4 NO3 whose ions have the same migration velocities. Then the ions
move with equal speed to anode and cathode compartments minimizing the junctions
potentials almost zero. A salt bridge is used to connect electrolytically, the two electrolyte
solutions of a galvanic cell, as shown in the Fig. 1.1.5.

Fig.1.1.5 Daniel Cell indicating the function of a salt bridge

The salt bridge consists of a saturated solution of a salt such as KCl or NH4 NO 3 , whose ions
have almost same migration velocities. The positive and negative ions of the salt in the salt
bridge migrate with equal speed into cathode and anode compartments respectively, thereby
minimizing liquid junction potential.
The salt bridge is prepared by dissolving 5g agar in 100 mL aqueous solution of KCl
containing 35 g of KCl and filling in a U-tube. On cooling, the agar forms a jell with KCl
solution in it. A salt bridge has the following functions:

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 1. It provides electrical contact between the two electrolyte solutions of a cell i.e., it
physically separates the two electrolytes but completes the electrical circuit by
altering ions causing charge to move from half-cell to the other.
2. It minimizes liquid junction potential in galvanic cells containing two electrolyte
solutions in contact. i.e., it reduces the LJP to a minimum by nearly equal diffusion
rates of cations and anions.
3. It maintains the electrical neutrality of the two half cells i.e., it prevents any net
charge accumulates in the two electrolytes.
1.1.6 ELECTROMOTIVE FORCE OF THE CELL
Electricity cannot flow from one electrode to another unless there is a potential
difference between the two points. The difference of potential, which causes a current to flow
from the electrode at higher potential to an electrode at lower potential is called the
“electromotive force”(e.m.f.) of the cell “or the “cell potential” and is expressed in volts V.
The emf of a cell is denoted by E cell .Mathematically,
Ecell = Ecathode- Eanode
The driving force that pushes the negatively charged electrons away from the anode and pulls
them towards the cathode is known as emf. The E Cell depends on the nature of the electrodes
composition, (combination of electrodes, strong tendency to lose or gain electrons produces
large cell potential) temperature (E∞T) and concentration of the electrolyte solutions. To
facilitate comparison of different galvanic cells, their standard emf, denoted by E 0 cell is used.
Standard emf of a cell is defined as the emf of a cell when the reactants & products of the cell
reaction are at a unit concentration or unit activity, at 298 K and at 1 atmospheric pressure
including pure solids and liquids.
The emf of a cell represents the driving force of a cell reaction. As represented by the
thermodynamic relation,
∆G = -nFE
Where ∆G is the free energy change accompanying a cell reaction, n is the number of
electron transfer during the cell reaction, and F is the Farad ay constant, F = eN A, the
magnitude of the charge per mole of electrons. Hence the above equation is the key
connection between the electrical measurements on the one hand and thermodynamic
properties on the other.
The cell reaction is spontaneous or feasible when ∆G is negative. ∆G can be negative only if
the emf of the cell is positive, because, the other two factors, n & F are always positive. Thus
emf of a galvanic cell is always positive. The positive emf value indicates the spontaneity of
cell reaction in the given direction. When the cell potential is large, a given number of

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electrons traveling between the electrodes can do a large amount of electrical work. When the
cell potential is small, the same number of electrons can do only a small amount of work. A
cell in which the overall reaction is at equilibrium can do no work, and then the cell potential
is zero.
1.1.7 Measurement of emf of a cell
The emf cannot be measured accurately by connecting directly a voltmeter between the
two electrodes, because during such a measurement, a part of the cell current is drawn to
deflect the needle as part of the emf is used to overcome the internal resistance of the cell.
Consequently, such a measurement would indicate a potential difference less than the actual
emf of the cell. For precise emf measurements potentiometers are used, which require
extremely small current at the balance point.
The potentiometric measurement of emf of a cell works based on Poggendorff’s
compensation method. In this method, emf of a test cell is opposed by the impressed emf
from an external source of emf, and the measurement is made when there is no net flow of
current in the circuit. The basic principle is that the emf of the cell to be measured is exactly
balanced by an equal and opposite known emf so that no current flows in the circuit (null
point) A schematic diagram of the potentiometer is shown in Fig.1.1.7
S Rh
+ - C

D D
A
B
Ex
J
G
Es

Fig.1.1.7. Potentiometric arrangement for the measurement of EMF of a galvanic

cell.1.1.5

AB- Potentiometric wire

S- Storage battery
ES- Standard cell
Ex- unknown cell
G- Galvanometer
J- Sliding contact.
Rh – adjustable resistance

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The two terminals of a storage battery(S) which has a constant and higher emf than the test
cell, is connected to two ends of a long uniform wire AB of high resistance. The positive
terminal of the test cell is connected to the end A, to which the positive terminal of S is
connected & the negative terminal is connected to a sliding contact J through a galvanometer
(G). The sliding contact is moved along the wire AB until the null point is reached, which is
indicated by no current flow in the galvanometer. The position of a null point is noted & the
distance AD is measured. The emf of the unknown cell E x is proportional to the length AD.
• Ex α AD
Then the test cell Ex is replaced by a standard cell Es, whose emf, is known the position of
the sliding contact is readjusted by moving it over AB, as before, till null point D 1 is
reached .The length AD 1 is measured. The emf of the standard cell E s is proportional to the
length AD 1 .
• Es α AD 1
• Ex ═ AD
• Es AD1
• Ex = AD x Es
AD I
Thus the emf of the test cell is calculated by substituting the emf of the standard cell in the
above equation.
1.1.8 Standard cell requirements:
1. Its emf should remain constant for a longer period of time.
2. It should be capable of providing highly reproducible emf.
3. The temperature coefficient of emf should be negligibility small i.e (δ E/ δT)= 0
4. The cell reaction should be reversible.
5. It should not be subjected to permanent damage due to the passage of current.
6. A standard cell is one which has a constant and reproducible known emf with a
negligible variation of emf with temperature e.g. Weston standard cell or Weston
cadmium cell.
1.2 Energetic of cell reactions:
1.2.1 The relation between E and ∆G:
A cell in which the overall reaction has not reached chemical equilibrium can do electrical
work as the reaction drives electrons through an external circuit. The work that a given
transfer of electrons can accomplish depends on the cell potential.

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The maximum electrical work as per thermodynamics, chemical reaction can do is given by
the value ∆G for the reaction.
We, max = ∆G----------------- 1
Where, We is electrical work. It follows that, to draw thermodynamic conclusions from
measurements of the work a cell can do, we must ensure that the cell is operating reversibly.
Only then it is producing maximum work and only then we can relate electrical work to ∆G.
Both these conditions are achieved by measuring the cell potential when it is
balanced by an exactly opposing source of potential so that the cell reaction occurs
reversibly, the composition is constant, and no current flows.
The net electrical energy and the emf of the cell produced in a cell is the product of the
quantity of electricity that passes through the cell and the emf of the cell.
We = QE Joules. -------(2)
Q is the quantity of electrical charge in coulombs produced by the reaction and E is the emf
of the cell in volts.
Charge on 1 mol (6.02 x 10 23 ) electrons is F coulombs, where F is Faraday constant. When n
electrons take part in the cell reaction, n mols of electrons are involved per mol of a reactant
of the reaction. Hence charge on n mol of electrons = nF coulombs. This is the charge, Q in
coulombs produced by the reaction. For 1 mole of electrons transferred in the cell reactions,
the quantity of electricity = 1F
If n moles of electrons are transferred in the cell reactions, the quantity of electricity = n F
Therefore electrical energy= nFE, ----------(3)
In a large number of reactions, electrical energy produced is not equal to chemical energy.
Electrical energy produced = decrease in free energy for cell reaction i.e. - ∆G = nFE or
∆G = -nFE Joules-------(4)
If we know emf E, ∆G can be calculated. The larger the value of cell potential the further the
reaction is equilibrium.
1.2.2 Relation between E and ΔH
Enthalpy Change ΔH = nF[T(δE/δT)P –E] --------(5)
If we know emf and temperature coefficient of emf, ΔH can be calculated..

1.2.3 Relation between E and ΔS :

ΔS = nF(δE/δT)P ------------------(6)
1.2.4 Numerical Problems
1. Emf of Weston Cadmium cell is 1.0183 V at 293 K and 1.0l81 V at 298 K. Calculate
∆G, ΔH and ΔS of the cell reaction at 298 K.

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 Solution:- ∆G: ∆G = - n FE n = 2 for the cell reaction;
F = 96,500 C E= 1.0181 V at 298 K
∆G = -2 x 96,500 x 1.0181 J = -196.5 KJ
∆H: ∆H = nF [ T (δE /δT)P – E]
(δE/δT)p = 1.0181 – 1.0183 / 298-293 = -0.0002 / 5
= - 0.00004VK -1
T = 298 K
∆H = 2 x 96,500 { [298 x (-0.00004)] – 1.0181}
= -198. 8 KJ
ΔS: ΔS = nF(δE / δT) P

= 2 x 96,500 x (0-00004) = -7.72JK -1

2. The emf of the cell Cd|CdCl2. 2.5 H2O (saturated) || AgCl(s)| Ag is 0.6753V and 0.6915 V at
298 K and 273 K respectively. Calculate ∆G, ΔH and ΔS of the cell reaction at 298 K.
Solution. Here n = 2, E = 0.6753 V at 298 K and 0.6915 at 273 K.
(δE/δT)p = (0.6753-0.6915) V/ (298-273) K = - 0.00065 V/K
Now at 298 K, ∆H = nF [ T (δE /δT)P – E]
= 2 mol x 96,500 C mol-1 { [298 K x (- 0.00065 V/K)] – 0.6753 V }
= -167. 7 KJ
∆G at 298 K ; ∆G = - n FE = -2 x 96,500 x 0.6753 = -130.33 KJ
ΔS = nF(δE / δT) P

= 2 x 96,500 x (0-00065) = -125.45 J.K -1

1.3 SINGLE ELECTRODE POTENTIAL

The potential of the single electrode is the difference of potential between a metal and
the solution of its salt. i.e the tendency of an electrode to lose or gain electrons when in
contact with its own ions in the solution. In a cell, the electrode with lower electrode potential
has less tendency to undergo reduction and acts as an anode. The electrode with higher
electrode potential has a higher tendency to undergo reduction and acts as a cathode.
Example: In case of Zn in ZnSO 4 solution acquires a negative charge (Fig. 1.3a).
M(s) → Mn+ + ne -(aq) (1) Dissolution reaction and conversely, the metal
shows the tendency to go into the solution as metal ion by losing electrons (Fig. 1.3b).
Mn+ (aq) + ne -(aq) → M(s) (2) Deposition reaction

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 Fig.1.3a. Zinc ions move Fig.1.3b.Copper ions get deposited as
into solution leaving behind copper leaving behind free negatively
electrons making it electron charged sulfate ions in solution makes the
rich electrode electron poor

The rate of this reaction depends on,

(i) the nature of the metal
(ii) the temperature
(iii) the concentration of metal ions in solution.

When a metal is placed in the solution of its own salt, the chemical reaction (1) or (2), takes
place depending on whether the dissolution reactions are faster than deposition or vice versa.
A dynamic equilibrium is established, because negative or positive charge developed on the
metal attracts the positively or negatively charged free ions in the solution. Due to this
attraction, the positive or negative ions remain quite close to the metal. Thus, a short layer of
positive ions or negative ions as in the figure is formed at the junction of the electrode and the
solution. This layer is called a Helmholtz electrical double layer. A difference of potential is
consequently, set up between the metal and the solution. This potential difference will persist
as long as the charge is allowed to remain on the metal; and this will prevent any f urther
passing of the positive ions from or to the metal. At equilibrium the potential difference
between the metal & solution becomes a constant value. The equilibrium potential difference
so established is called the “electrode potential” of the metal. Thus, the electrode potential of
a metal is the measure of the tendency of a metallic electrode to lose or gain electrons, when

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it is in contact with a solution of its own salt of unit molar concentration at 298K.
Consequently, the tendency of an electrode to lose electrons is a direct measure of its
tendency to get oxidized & this tendency, is called oxidation potential. Similarly, the
tendency of an electrode to gain electrons is a direct measure of its tendency to get reduced
and this tendency is known as reduction potential. By concentration, electrode potential refers
to reduction potential.
1.3.1 Measurement of electrode potential
It is impossible to determine the absolute half cell potential We can only measure the
difference in potential between two electrodes potentiometrically, by combining them to form
a complete cell. All voltage measuring devices determine differences in potential. If one knob
of voltameter is connected to a test electrode, another one will make contact with the solution
in the electrode compartment via another conductor. This second contact involves solid/
solution interface and acts as a record half cell. The redox reaction must take place if the
charge is to flow and potential is to be measured. A potential is associated with this second
reaction and absolute half cell potential is not obtained. What we measure ultimetaly is the
difference between the half cell potential of test electrode and a half cell made up of the
second contact and the solution. Therefore, absolute electrode potentials cannot be measured.
We can only determine the relative value of electrode potential, if we can fix arbitrarily the
potential of any one electrode. For this purpose, the potential of a standard hydrogen
electrode (SHE) or normal hydrogen electrode (NHE) (i.e., a platinum electrode in contact
with 1 M H + ion concentration and hydrogen gas at 1 atmospheric pressure is constantly
bubbled through it) has been arbitrarily fixed as zero and the numerical values of electrode
potentials of different electrodes are relative values w.r.t SHE. Therefore, single electrode
potentials of electrodes are referred to as potentials on the hydrogen scale.
Sign of electrode potential: When an electrode is coupled with a SHE, if reduction occurs
then EP is given a +ve sign e.g Copper electrode + SHE
• Cu2+ +2e- → Cu(s) reduction at copper electrode (cathode)
• H 2 (g) → 2H + +2e- oxidation at hydrogen elecrode (anode) → E0 = 0.34 volt
A +ve sign on the EP value indicates that the half cell acts as cathode and acepts electrons
from the hydrogen electrode.
Similarlly, when an electrode is coupled with SHE, if oxidation occurs then EP is given a -ve
sign e.g . Zinc electrode + SHE
• Zn (s) → Zn2+(aq) +2e- (oxidation at Zinc elecrode)
• 2H + (aq) + 2e -→ H 2 (g) (reduction at Hydrogen elecrode) → E0 = - 0.76 volt

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A –ve sign on the electrode potential value indicates that the half cell acts as an anode by
releaseing electrons to the hydrogen electrode.
1.3.2 Standard electrode potential:
Standard electrode potential is the electrode potential when the electrode is in contact with a
solution of unit concentration at 298 K involving pure solids and liquids. If the electrode
involves a gas, then the gas is at 1 atmospheric pressure. It is denoted by Eo . When elements
are arranged in increasing order (downwards) of their standard electrode potential, a series
called electrochemical series is obtained. In a cell, the electrode with lower electrode
potential has less tendency to undergo reduction and it acts as anode similarly electrode with
higher electrode potential has higher tendency to undergo reduction and acts as cathode.
Reducing agents Stable ions Electrode half reaction E 0 volts
Lithium Li+ -3.03
Potassium K+ -2.92
Aluminium Al3+ -1.66
Zinc Zn2+ -0.76
Iron Fe3+ -0.44
Lead Pb2+ -0.13
H2 2H+ 0
Copper Cu2+ 0.34
Silver Ag+ 0.80
Gold Au3+ 1.52

Fig. 1.3.2. Selected standard electrode potentials

1.3.3 Nernst equation

Nernst equation is an expression of a quantitative relationship between electrode

potential/cell potential and concentration of the electrolyte species in an electro-chemical
reaction. i.e. mathematical expression that relates the potential of an electrode to the
concentrations of those species in solution that are responsible for the potential. Consider a
general redox reaction: Mn+(aq) + ne- M(s)
E = Eo + 2.303RT/nF log [Mn+]

E= Electrode potential at some moment in time

E0 = Standard electrode potential

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R= Universal gas constant (joules per mol K)

T= Temperature in Kelvin scale F= Faraday constant (96,500 Coulumbs)

n = Number of electrons transferred in the half reaction/ cell reactions
[Mn+]= Concentration of metal ion at that moment in time (moles per litre).
At 298 K, when the values of R.T and F are substituted, the equation reduces to,

E = Eo + (0.0592/n) log [Mn+]

This expression is known as the Nernst equation for electrode potential at 298 K. From these
equations, it is clear that,
i) If the concentration of the solution (Mn+) is increased, the electrode potential
increases and vice versa.
ii) If the temperature is increased, the electrode potential increases and vice versa.

The Nernst equation can also be applied for the calculation of emf of a cell. Consider the cell
reaction aA+ bB cC +dD
The Nernst equation for the emf of the cell is

Ecell = Eo cell – 2.303RT/nF log [C]c [D]d /[A]a [B]b

At 298 K,

Ecell = Eo cell – (0.0591/n) log [C]c [D]d /[A]a [B]b

Where n is the number of electrons transferred during the cell reaction and Eo cell is the
standard emf of the cell.
1.3.3.1 Significance of the Nernst equation

1. It can be used to calculate the potential of a cell that operates under non-standard
conditions. The Nernst equation tells us that a half-cell potential will change by 59 millivolts
per 10-fold change in the concentration of a substance involved in one-electron oxidation or
reduction; for two electron processes, the variation will be 28 millivolts per ten fold
concentration change. Thus for the dissolution of metallic copper
Cu(s) → Cu 2+ + 2e–

the potential E = (– 0.337) – .0295 log [Cu 2+] becomes more positive (the reaction has a
greater tendency to take place) as the cupric ion concentration decreases.
2. It can be used to measure the equilibrium constant for a reaction. At equilibrium the
overall cell potential for the reaction is zero. i.e. E=0
Nernst equation,

16
0 = Eo - RT/nF lnK c
Kc = e nFE° / RT

1.4 Calomel electrode

The calomel electrode (Fig.1.4.1), a mercury mercurous chloride electrode develops + 0.242
V at 289 K when the KCl solution is saturated. It has been found that the potential of the
calomel electrode, on the hydrogen scale varies with the concentration of the potassium
chloride solution used. The concentration of KCl solution used is either decinormal, normal
or saturated. Correspondingly, the electrode is known as decinormal, normal or saturated
calomel electrode respectively.

1.4.1 Construction & Working:

Fig.1.4.1 Schematic diagram of calomel electrode.

It consists of a tube, in the bottom of which is a layer of mercury, over which is placed a paste
of mercury and mercury chloride.The remaining portion of the cell is filled with a solution of
normal or decinormal or saturated solution of KCl. A platinum wire sealed at its end fixed
into the main tube dipping into the mercury layer is used for making electrical contact. The
electrode can be represented as Hg (l) /Hg2 Cl2 (sat’d) /KCl-(sat’d/ xM)

17
The calomel electrode can act as anode or cathode depending on the nature of other electrode
of the cell. When it acts anode, the electrode reaction is
• 2Hg (l) → Hg2 2+ (aq) + 2e-
• Hg2 2+(aq) + 2Cl- (aq)→Hg2 Cl2
----------------------------------------------------

• 2Hg(l) + 2Cl- (aq) → Hg2 Cl2 (s)+ 2e-

When it acts as cathode, the electrode reaction is,
• Hg2 2+(aq) + 2e-→ 2Hg(l)
• Hg2 Cl2 (s) → Hg2 2+ (aq) + 2Cl-
__________________
• Hg2 Cl2 (s) + 2e- → 2Hg (l) + 2 Cl-(aq)

The net reversible electrode reaction is,

Hg2 Cl2 (s) + 2e- 2 Hg (l) + 2 Cl-(aq)

Electrode potential is given by

E = Eo – 2.303 RT log [Cl-]2

2F

= Eo - 0.0591 log [Cl-] at 298 K

1.4.2 Uses:

Since the electrode potential is a constant it can be used as a secondary reference electrode to
replace the inconvenient SHE for potential measurements.
i) To determine the electrode potential of the unknown electrode
For example: The test electrode, Zn(s) /Zn2+(aq) is coupled with a saturated calomel electrode.

Zn(s) / Zn2+ (aq) ││ Cl- (saturated soln) /Hg2 Cl2(s) / Hg (l)

The emf of the so formed cell is determined experimentally by potentiometric method.

Then
E cell = E cathode – Eanode = 0.2444 – Ezn
Ezn = 0.2444 – E cell
ii) To determine the pH of a solution cell: Hg(l) / Hg 2 Cl2 (s) // H + /pt,H 2 (g)
E cell = E cathode – E anode

= 0.242 – (- 0.0592 pH)

18
 pH = E cell – 0.242/0.0592
1.4.3 Advantages

➢ It is very simple to construct.

➢ It can be used for a long time without much attention.

➢ Electrode potential is stable over a long period (reproducibly).

➢ It hashes the low temperature coefficient of emf.

➢ It is less prone to contamination because the mercury/ mercurous chloride interface is

protected inside a tube not in direct contact with the electrolyte.
1.4.4 Disadvantages

➢ Calomel electrodes should not be used above 50 o C because the mercurous chloride
breaks down, yielding unstable readings. This is important if substantial temperature
changes occur during measurement.
➢ Calomel electrode should be used with proper precaution as mercury compounds are
toxic.

1.5 Ion Selective Electrode.

The electrode which is sensitive to a specific ion present in an electrolyte whose

potential depends upon the activity of a specific ion in the electrolyte is called an ion selective
electrode. The magnitude of the potential of this electrode is an indicator of the activity of the
specific ion in the electrolyte. Example for this type of electrode is glass electrode.
1.5.1 Glass electrode: Construction

19
 Glass Membrane
Electrical contact

Protective sleev
e

Ag/AgCl wir
e

HCl, 0.1 molmd-3(Referrence solution of dilute

HCl)
Thin wall
ed glass Outer Inner
membrane
E1 E2
Solutionof
unknownpH

Fig.1.5.1a. Schematic diagram of the Glass Fig. 1.5.2b. Line sketch of a glass membrane
electrode showing outer analyte solution and internal
reference solution.

The electrode consists of a thin glass membrane, typically about 0.03 to 0.1 mm thick, sealed
onto one end of a heavy–walled glass tube. A special variety of glass (corning 0l5 glass with
approximate composition 20 % Na2 O, 6 % CaO & 72 % SiO 2 ) is used which has a low
melting point and high electrical resistance. The glass bulb is filled with a solution of
constant pH (0.1 M HCl). A small volume of saturated silver chloride is contained in the tube.
A silver wire in this solution forms a silver/silver chloride reference electrode which is
connected to one of the terminals of a potential measuring device. The internal reference
electrode is a part of the glass electrode and it is not the pH sensing element. Only the
potential that occurs between the outer surface of the glass bulb and the test solution responds
to pH changes.
1.5.2 Working: A silicate glass used for membranes consists of an infinite 3D- network of
SiO 4 4- groups in which each silicon is bonded to four oxygen and each oxygen is shared by
two silicons. There are sufficient cations to balance the negative charge of the silicate groups
within the interstices of this structure. Singly charged cations such as sodium and lithium are
mobile in the lattice and are responsible for electrical conduction within the membrane. The
glass is a partially hydrated aluminosilicate containing sodium or calcium ions. The

20
hydration of a pH sensitive glass membrane involves an ion -exchange reaction between
singly charged cations in the interstices of the glass lattice and protons from the solution. The
process involves univalent cations exclusively because divalent cations are too strongly held
within the silicate structure to exchange with ions in the solution and hence immobile. The
ion-exchange reaction can be written as

• H+ + Na+ Na+ + H+
Solution glass solution glass

The Na+ ions on the glass membrane are exchanged for H + ions in the solution. The potential
of the electrode is controlled by the difference between the hydrogen ion concentration inside
and outside the thin glass membrane. Since the H + ion concentration inside the electrode is
constant, the electrode’s potential varies only with the concentration of H + in the solution
outside. Thus the potential arises from the difference in positions of ion-exchange
equilibrium on each of the two surfaces. The surface exposed to the solution having the
higher H + concentration becomes positive with respect to the other surface. This charge
difference or potential serves as the analytical parameter when the pH of the solution on one
side of the membrane is held constant. Evidently the selectivity of glass electrodes is related
both to the ability of the various monovalent cations to penetrate into the glass membrane and
to the degree of attraction of the cations to the negative sites within the glass.
1.5.3 Electrode Potential of GE

The overall potential of the glass electrode has three components; 1) The boundary potential
Eb , which varies with the pH of the analyte solution. It is made up of two potentials, E 1 & E2
which develop at the two surface of the glass membrane i.e. the potential developed at the
inner glass surface & the potential developed at the outer glass surface.
Eb = E1 -E2 _______________________ (1)

Where Eb is the boundary potential

E1 = potential developed at the interface between the exterior of the glass and the
analyte solution
E2 = Potential developed at the interface between the internal solution and the interior
of the glass. The boundary potential is related to the concentration of hydrogen
ion in each of the solution by the Nernst-like equation.

21
Eb = E1 – E2 = 0.0592 log Cl / C2 _________________ (2)

Where C1 = concentration of the analyte solution

C2 = concentration of the internal solution

For a glass pH electrode the hydrogen ion concentration of the internal solution is held
constant.

So eqn. (2) becomes

Eb = K + 0.0592 log C 1 __________________(3) (Recall pH= -log [H +]

Eb = K - 0.0592 log pH where K= -.0592 log C2

The boundary potential is then a measure of

1) the hydrogen ion concentration of the external solution.

2) The potential of the internal Ag/AgCl reference electrode. E Ag/AgCl.

3) A small unpredictable contribution called the asymmetry potential, E asym .

The sources of the asymmetry potential include the following.
i) Differing conditions of strain in the two glass surfaces during manufacture

ii) Mechanical abrasion on the on the outer surface during use

iii) Chemical etching of the outer surface during use.
The asymmetry potential changes slowly with time. The glass electrode potential can be
written in the equation form as
EG = Eb + EAg/ AgCl + E asym __________________ (4)

Substitution of eqn – (3) for Eb , gives

EG = K + 0.0592 log C 1 + EAg/AgCl + E asym

= K – 0.0592 log pH + E Ag/AgCl + E asym ___(5)

EG = Eo G – 0.0592 pH __________________(6)
where Eo G = K + EAg/AgCl + E asym. a combination of three constant terms = constant To
measure the hydrogen ion concentration of the test solution, the glass electrode (indicator
electrode) must be combined with an external reference electrode, which is required for all
kinds of ion-selective electrode determinations.
1.5.4 Applications: Determination of pH:
The glass electrode has an emf that changes with hydrogen ion concentration, i.e the glass
electrode is the most important indicator electrode for hydrogen ion. It is used for the

22
measurement of pH under many conditions and normally calomel electrode is used as
reference electrode to complete the cell (Fig.1.4.4)
Cell: SCE / Test solution / GE

Fig.1.4.4. Set up of indicator electrode and reference electrode for the measurement of pH.

E cell = E glass – E calomel where E glass = the E.P. of the glass electrode.

E calomel = the E.P. of the SCE

E cell = Eo G – 0.0592 pH – 0.2444

The Eo G value of a glass electrode can be determined by dipping the glass electrode in a
solution of known pH. Typical fields are the clinical & food analysis, environmental
monitoring (industrial waste acidity of rain) and process control (fermentation, boiler w ater,
galvanization & precipitation)

1.5.5 Advantages:

➢ It can be used without interference in solutions containing strong oxidants, strong

reductants, proteins, viscous fluids and gases as the glass is chemically robust.
➢ The glass electrode gives accurate results in the pH range 2 – 10. With some special
glass (by incorporation of Al2 O 3 or B2O3 ) measurements can be extended to pH
values up to 12.
➢ It is immune to poisoning and is simple, robust and easy to operate.

➢ The equilibrium is reached quickly & the response is rapid.

23
 ➢ It can be used for very small quantities of the solutions. Small electrodes can be used
for pH measurement in one drop of solution in a tooth cavity or in the sweat of the
skin (micro determinations using microelectrodes)
➢ The glass electrode is much more convenient to handle than the inconvenient
hydrogen gas electrode.
➢ Glass electrodes which are selective for Li+, Na+, Cs+, Ag+ and NH4 + ions are
commercially available and these special electrodes are useful for measuring the
above ions.
1.5.6. Disadvantages:

➢ The bulb of this electrode is very fragile and has to be used with great care. The
sensitive tip is easily scratched and ruined.
➢ The alkaline error arises when a glass electrode is employed to measure the pH of
solutions having pH values in the 10-12 range or greater. In the presence of alkali
ions, the glass surface becomes responsive to both hydrogen and alkali ions. Hence
the measured pH values are low and thus the glass pH electrode gives erroneous
results in highly alkaline solutions.
➢ The acid error results in highly acidic solutions (pH less than zero) Measured pH
values are high.
➢ Dehydration of the working surface may cause erratic electrode performance. It is
crucial that the pH electrode be sufficiently hydrated before being used. When not in
use, the electrode should be stored in an aqueous solution because once it is
dehydrated; several hours are required to rehydrate it fully.
➢ As the glass membrane has a very high electrical resistance (50 to 500 MΩ), the
ordinary potentiometer cannot be used for measurement of the potential of the glass
electrode. Thus special electronic potentiometers are used which require practically
no current for their operation.
➢ Standardization has to be carried out frequently because asymmetry potential changes
gradually with time. It is better to determine E o G for a glass electrode before use.
➢ The commercial version is moderately expensive.
➢ To some extent, the constant E oG is a function of the area of glass in contact with the
acid analyte. For this reason, no two glass electrodes will have the same value of E o G.
Note that EoG depends on a particular glass electrode used & it is not a universal
constant.
1.6 BATTERY TECHNOLOGY

24
1.6.1 Introduction
Can you imagine a world without batteries? The clock on your wall requires a battery for it to
work. The watch on your wrist goes on a battery. The motor vehicle needs a battery for it to
start and take you to your destination. Battery is the backbone of UPS to run your computer
without interruption. After a days work, if you pick-up the remote control of the television, it
is again the battery that helps you to change channels of the T.V. Cameras, laptop computers,
cellular phones, key chain laser, heart pacemaker and children toys – they all require
batteries.
Batteries are used for so many different purposes and different applications require batteries
with different properties. The battery required to start a car must be capable of delivering a
large electrical current for a short period of time. The battery that powers a cardiac
pacemaker must be small, rugged, leak proof, compact and capable of delivering a steady
current for an extended period of time. In UPS systems, longer and consistent backup is
needed. Batteries for hearing aids must be above all tiny. Batteries for torpedoes and
submarines must be stable during storage and give high power for short times & certainly
rechargeable. For a lap-top computer, a battery in the form of a flexible sheet distributed
around the case is much preferred. Batteries remain an enormous industry with a turnover of
billions of pounds worldwide.

1.6.2 Classification of commercial cells

Primary Cells: They are galvanic cells which produce electricity from chemicals that are
sealed into it when it is made. This type of cells cannot be recharged as the cell reaction
cannot be reversed efficiently by recharging. Once the cell reaction has reached equilibrium
the cell must be discarded. No more electricity is generated and we say the battery is ‘dead’.
These are also known as ‘throw – away’ batteries or irreversible batteries.
Eg: Dry cell, Lithium copper sulfide cell
Secondary cells: A secondary cell is rechargeable by passing current through it. In the
charging process, an external source of electricity reverses the spontaneous cell reaction and
restores a non- equilibrium mixture of reactants. After charging, the cell can be used for
supplying current when required, as the reaction sinks toward equilibrium again. Thus as the
secondary cell can be used through a large number of cycles of discharging and charging.
Such cells are also known as rechargeable cells, storage cells, or accumulators.
Eg. Lead-acid batteries, Nickel-cadmium cell, Lithium- ion battery
1.6.2.1 Requirements of Primary Battery:
• Compact, lightweight and must be fabricated from easily available raw materials.

25
• Economic and have benign environmental properties
• Should have a high energy density, longer shelf life
• Provide constant voltage and should have a long discharge period
1.6.2.2 Requirements of Secondary Battery
• Long shelf-life in both charged & discharged conditions
• Longer cycle life and design life
• High power to weight ratio
• Short time for a recharge.
• High voltage & high energy density
1.6.2.3 Differences between Primary and Secondary batteries
Primary Batteries Secondary Batteries
1.Cell reaction is irreversible Cell reaction is reversible
2. They must be discarded after its They may be recharged a number of
active elements have been consumed times from an external d.c. source
during its useful life
3. Have a relatively short shelf life Have a very long shelf life
4. Function only as galvanic cells Function as galvanic cells during
discharge as & as electrolytic cells
during the charging process.
5. They cannot be used as energy They can be used as energy storage
storage devices devices (e.g. solar/ thermal energy
converted to electrical energy)

6. They cannot be recharged They can be recharged.

e.g. Dry cell, Li-MnO2 battery e.g.Lead acid battery, Ni-cd battery

1.6.3 Lead Storage Battery (Lead Accumulator or Car Battery or The acid battery)
Construction: The electrodes are lead grids to maximize its surface area. The anode grid is
filled with finely divided spongy lead (Pb) and the cathode grid is packed with lead dioxide
(PbO 2 ). Both electrodes are submerged in a sulfuric acid solution (H 2 SO4 ) having a specific
gravity of about 1.25 that acts as the electrolyte. Anode and cathode grids are separated by
insulators like strips of wood, rubber or glass fiber. In car batteries, six cells are connected in

26
series (anode to cathode) to produce a 12–volt battery. The battery is encased in a plastic
container or hard vulcanized rubber vessel. The cell doesn’t need to have a separate anode
and cathode compartments because the oxidizing and reducing agents are both solids (PbO 2 &
Pb) that are kept from coming in contact by the presence of insulating spacers between the
grids. Both anode and cathode are immersed in a common electrolyte (i.e. cell without liquid
junction). This is an example of a ‘wet cell’, because the electrolyte is an aqueous solution
of sulphuric acid. The lead acid battery is very widely manufactured – 300 million units are
made each year.
At the cathode:
• PbO 2 (s) + 4H+(aq) + 2e− → Pb2+(aq) + 2H2 O (l)
• Pb2+(aq) + SO 4 2−(aq) → PbSO 4 (s)
____________________________________________________
• PbO 2 (s) + 4H+(aq) + SO 4 2−(aq) + 2e− → 2 PbSO 4 (s) + 2H 2 O (l)
_____________________________________________________

Overall: Pb(s) + PbO 2 (s) +4H+(aq) + 2SO 4 2−(aq) → 2PbSO 4 (s) + 2H 2 O(l)
Explanation:At the anode, lead atoms lose two electrons (e-) and become positively charged
lead ions (Pb2+). The lead ions combine with the sulfate ions (SO42-) in the sulfuric acid
solution to produce lead sulfate (PbSO 4 ). At the cathode, lead dioxide gains electrons,
releasing oxygen, which attaches to hydrogen ions (H+) to produce water (H 2 O (l) and lead
ions. The lead ions react with sulfate ions to produce lead sulfate. As this reaction progresses,
the flow of electrons creates an electric current. Lead sulfate adheres on each electrode and
water increases. The concentration of sulfuric acid decreases and the amount of lead and lead
dioxide decrease. When the reactants are depleted, the battery stops producing electricity.
The reaction can be reversed by recharging the battery & the PbSO 4 formed during discharge
remains adhered on each electrode and is available at the site during recharging. The nominal
voltage of each cell is about 2.1 V. The lead storage battery is designed to operate reversibly,
so that it can be used for the storage of electrical energy. They are called storage batteries
because their essential function is to store electrical energy. It is used to store energy in
chemical form.
Reactions during Charging:
Anode: PbSO4 (s) + 2e- → Pb(s)+ SO 4 2-(aq)
Cathode: PbSO 4 (s) + 2H2 O(l) → PbO 2 (s) + SO 4 2-(aq) + 4H +(aq) +2e-
Net reaction: 2PbSO 4 (s) + 2H2 O (l) → Pb(s) + PbO 2 (s) +2H 2 SO4

27
Recharging is possible because PbSO 4 formed during discharge adheres to the electrodes. By
attaching an external power source to a battery ( >2 volts), a current runs through the poles in
the opposite direction from normal discharge. This changes the lead sulfate and water back
into the original reactants, lead dioxide and sulfuric acid, i.e. the electrodes return to their
former composition and the sulfuric acid is regenerated. Charging, therefore, produces a
gradual increase in the sulfuric acid concentration. Since the level of charge on a storage
battery is related to sulfuric acid concentration, the specific gravity of the H2 SO4 solution is
a measure of the operational condition of a battery. A charged battery at room
temperature with its electrolyte at normal concentration supplies a potential difference of 2.1
to 2.2 V. The complete reaction cycle of a lead acid storage battery is as follows.

Disch
Pb(s) + PbO 2 + 2 H2 SO4 (aq) arge 2 PbSO 4 (s) + 2 H2 O(l)
H2 SO4 Ch
arg
In an automobile, the energy necessary for recharging the battery is provided by the generator
driven by the engine. As the external source forces electrons from one electrode to another,
the PbSO 4 is converted to Pb at one electrode & to PbO 2 at the other.
Overcharging:
Electrolysis of water: The net reaction can be summarized by the equation.
2H2 O (l) + electrical energy → 2H 2 (g) + O2 (g)
No gases will be liberated on charging as long as lead ions are present in solution. If the
electrolysis is permitted to proceed further, hydrogen gas is formed at the cathode and oxygen
gas is evolved at the anode. The hydrogen ions are discharged at the cathode through the
reaction
2H+(aq) + 2e -→ H2 (g)
Sulphate ions are resistant to oxidation and are not discharged at the cathode. Water is
oxidized at the anode in preference to SO 4 2-
2H2 O(l) →O2 (g) + 4H+(aq) +4e -
Consequences: (i) Excessive charging may reduce the acid level and may damage the
exposed electrode grids (ii) In extreme cases, there will be dangerous high-pressure build-up
that can lead to a serious risk of explosion. In more normal circumstances, the older version
of the battery needs to be ‘topped up’ from time to time.
Recent years have seen the introduction of “maintenance – free batteries” without a gas –
release vent. Here the gassing is controlled by careful choice of the composition of the lead
alloys used i.e. by using a Pb-Ca (0.1 % ) as the anode which inhibits the electrolysis of
water.

28
Alternatively, some modern batteries contain a catalyst (e.g. a mixture of 98% ceria (cerium
oxide) & 2% platinum) that combines the hydrogen and oxygen produced during discharge
back into the water. Thus the battery retains its potency and requires no maintenance. Such
batteries are sealed as there is no need to add water and this sealing prevents leakage of cell
materials.
Applications: The many battery designs available for a wide variety of uses can be classified
into three main categories. (a) Automotive (b) Industrial & (c) Consumer batteries.
The automotive type is used in cars and trucks, to provide a short burst of power for starting
the engine. It is incorporated as an essential accessory into the starting circuit of internal
combustion engines for starting, lighting & ignition (SLI). Units normally have nominal
voltages of 12 V for LMVS and 24 V for HGVS. It is still playing a major role in
transportation, powering literally millions of ICES in automobiles. The industrial batteries are
used for heavy–duty applications such as motive and standby power. This class of batteries is
used to operate electric trucks, submarines and mine locomotives. They also provide power
for the air conditioning and lighting systems. It is used in the stationary back–up power
applications such as telecommunication systems, to ensure that, for example, the telephone
network will continue to operate even in the event of a mains power failure. Such batteries
are kept in hospital operating theaters, railway signal centres and other places where a power
failure might be disastrous and is used to supply electrical power during emergencies.The
consumer batteries are used in aemergency lighting systems, security and alarm systems,
public address systems, power tools, UPS in computers, and small engine starting including
electronic vehicles.
Advantages:
• A lead storage battery is highly efficient. The voltage efficiency of the cell is defined
as follows.
• Voltage efficiency = average voltage during discharge
• average voltage during charge
• The voltage efficiency of the lead – acid cell is about 80 %.
• The near reversibility is a consequence of the faster rate of the chemical reactions in
the cell i.e. anode oxidizes easily and cathode reduces easily leading to an overall
reaction with a high negative free energy change.
• A lead – acid battery provides a good service for several years. The number of
recharges possible range from 300 to 1500, depending on the battery’s design and

29
 conditions. The sealed lead-acid batteries can withstand up to 2000 – recharging.
Time required for recharging is relatively low i.e about 2-8 hours.
• The battery has low internal self – discharge.
• A typical car battery provides a voltage of 12 V. This is not a large voltage, but the
battery can provide a large current. E.g. over 10 A, without being destroyed.
Disadvantages:
• If left unused in partially charged condition, it can be ruined in a short time by
nucleation and the growth of relatively large PbSO 4 crystals, which are not easily
reduced or oxidized by the charging current. This disaster is known as ‘sulfation’.
• The lead acid battery has low energy storage to weight ratio i.e. its chief
disadvantages is its great weight.(energy density ~ 35 wh / kg)
• The cell potential decreases with a decrease in concentration of sulfuric acid. During
the discharge process sulfuric acid is consumed and water is produced. So the solution
of sulfuric acid in the cell becomes less concentrated. The state of charge of the cell
can be judged by the concentration of sulfuric acid in the liquid and this is usually
done with a simple device to measure the density of the liquid. The density of a
healthy, fully charged battery is ≥ 1.25 g/mL.
• The battery is not efficient at a lower temperature. Foe a battery to function properly,
the electrolyte must be fully conducting. There will be an increase in the viscosity of
the electrolyte due to a decrease in the temperature. This leads to a decrease in the cell
potential.
• Overcharging may damage the exposed electrodes and may also lead to an explosion
in extreme cases. Sulfuric acid is highly corrosive liquid. In the event of an explosion,
the electrolyte is sprayed on to the individual who is working on the battery.
Therefore, safety goggles must be worn when working with these batteries.
• Lead is toxic and hence environmental & health problems arise due to careless
disposal by consumers.
• The corrosion of the lead grid at the lead dioxide electrode is one of the primary
causes of lead acid battery failure.
1.6.4 Nickel-Cadmium Cell
Construction: NiCad cell consists of a nickel wire gauze electrode grids. The anode grid
consists of spongy cadmium metal and the cathode grid contains the nicked (III) compound
NiO(OH). The electrolyte is a concentrated solution of KOH. It is the electrolyte of choice
because of its compatibility with the various electrodes, good conductivity and low freezing

30
point temperature (about – 30o C). Anode and cathode are separated by a very thin separator.
The contents are encased as a sealed unit in a steel case.

Figure 1.6.4 Schematic representation of NiCad cell

Working:
Discharging reactions
Anode: Cd (s) + 2OH -(aq) → Cd(OH)2 (s) + 2e-
Cathode: 2NiO(OH)(s) + 2H2 O + 2e- → 2Ni(OH)2 (s) + 2OH -(aq)
___________________________________________________
Cd (s) + 2NiO(OH)(s) + 2H2 O → 2 Ni(OH)2 (s) + Cd(OH)2 (s)
Charging reactions:
Anode: Cd(OH)2 (s) + 2e-→ Cd (s) + 2OH -(aq)
Cathode: 2 Ni(OH)2 (s) + 2OH -(aq) → 2 NiO(OH)(s) + 2H2 O+2e-
____________________________________________________

Overall reaction: 2 Ni(OH)2 (s) + Cd(OH)2 (s) → 2 NiO(OH)(s) + Cd (s) +2H2 O(l)
Explanation: At anode cadmium metal undergoes oxidation from 0 to +2, leaving behind
two electrons for every atom oxidized, as the cell discharges. At cathode nickel is reduced
from the +3 oxidation state (in nickel oxide hydroxide) to +2 (in nickel hydroxide). Note that
OH - is not used up as the cell is discharged. Therefore, there is no voltage drop through most
of the useful life of the battery as it discharges. The net reaction can take place until the
active materials are exhausted, during charging process, the cadmium hydroxide is re-
converted into cadmium and the nickelous hydroxide is reconverted to nickeloxide
hydroxide. The overall chemical reaction of the Ni-Cd system may be represented as

Cd + 2 NiO(OH) + 2H2 O Cd(OH)2 + 2Ni(OH)2

The cell must be recharged by applying the correct dc charging voltage.

31
Applications: Nicad cells are available in standard sizes (AA, D, C,F etc.) for use in flash
lights, photoflash units and portable electronic equipment such as radios, micro tape
recorders, calculators, cordless phones, electronic shavers, drills & garden tools. It is also
used in emergency lighting systems, alarm systems, personal audio equipment (walkman type
cassette players), kitchen appliances and other battery powered small tools, toys & games.
Advantages:
➢ Ni-cad batteries can be recharged many times because the solid products of the electrode
reactions adhere to the surface of the electrodes. Normally this battery can withstand up
to 3000 – recharging (longer cycle life)
➢ They maintain nearly constant voltage level throughout their discharge. Note that there
is no change change in the electrolyte composition during the operation.
➢ It can be left unused for long periods of time at any state of charge without any
appreciable damage (i.e. long shelf life).
➢ It can be encased as a sealed unit like the dry cell because gassing will not occur during
nominal discharging or recharging.
➢ They possess a longer design life. It can be extended upto 30 years or more if
maintained.
➢ They exhibit good performance ability at low temperatures.
➢ They can be used to produce large instantaneous currents as high as 1000-8000 A for one
second.
Disadvantages:
➢ It poses an environmental pollution hazard due to careless disposal by consumers and
produces health problems (decreases range from asthma to cancer) due to higher toxicity
of metallic cadmium than lead.
➢ Cadmium is a heavy metal and its use increases the weight of batteries, particularly in
larger versions. The energy density is approximately 40 Wh/kg.
➢ Cost of cadmium metal and hence the cost of construction of NiCad batteries is high.
The overall capital cost of these batteries is roughly then higher than that of lead storage
batteries.
➢ The KOH electrolyte used is a corrosive hazardous chemical. It is a poison and if
ingested attacks the throat and stomach linings. Eye contact can result in serve burns and
blindness. Protective clothing and face shields or goggles should be worn while
performing maintenance work.
1.6.5 Lithium ion cells

32
Lithium metal cannot be used safely in secondary batteries. Hence, various lithium
compounds have been made, which are used in rechargeable batteries, commonly known as
Lithium –Ion Cells. In these type of batteries, a lithiated metal oxide such as LiCoO 2,
LiV 2 O5 , LiMn2 O4 etc is inserted into the cathode which consists of a layered graphite crystal.
The electrolyte is normally LiPF 6 , but LiBF4 can also be used as LiPF6 is not corrosion
resistant.
Construction:
The anode is a lithium-carbide type intercalate (Lix C6 ). The cathode is a transition metal
oxide MO2 of variable oxidation state (MnO 2 , CoO2 , NiO2 ) which can intercalate lithium
usually cobalt dioxide, CoO 2 is used. The electrolyte is usually inert polar dry ether or
carbonate (diethyl carbonate or propylene carbonate), in which a conductivity salt such as
LiPF6 or LiBF4 is dissolved.

Figure 1.6.5 Schematic diagram of Rechargeable lithium ion battery

Working: Graphite has a layered structure and its electrochemically reduced in an aprotic
organic electrolyte containing lithium salts and lithium in interclated (or doped) between the
layers of graphite to form Lithium-Graphite interclated compound (GIC). Li-GIC undergoes
oxidation leaving an electron.
At anode:
⚫ Lix C6 xLi+(solv) + 6C(s) + xe-………………………….(1)
When a negative electrode is discharged, lithium is deinterclated (undoped) from lithiated
graphite and lithium ions dissolve into the elctrolyte. The lithium content in the LiCoO 2
electrode reversibly changes during charge and discharge as indicated in the following
equation:
At cathode:
⚫ CoO 2 (s) + xLi+(solv) + xe- Lix CoO 2 (s)……………….(2)

33
Net cell reaction:
Lix C6 (s) + CoO 2 Discharge Lix CoO 2 (s) + 6C………………….(3)
Charge
Explanations: It is called as a lithium ion battery to emphasise that it contains no lithium
metal. Both the electrodes are intercalation compounds. The electrode on the left serves as the
anode when the cell discharges. It is a special intercalation compound consisting of a graphite
host into which lithium ions have been electrochemically inserted between the carbon atom
layers. The lithiated graphite is written as Lix C6 . During the discharge, the lithium ions are
extracted by the half-reaction (1). The electrode that serves as cathod e during discharge is
normally cobalt dioxide. The reduction half reaction is cathode during discharge is normally
cobalt dioxide. The reduction half reaction shown in eq.(2), where cobalt undergoes reduction
from IV to III oxidation state. The overall reaction is shown in eq.(3). During discharge the
Li+ ions spontaneously migrate from the lithium graphite anode to the CoO2 cathode
enablingcurrent to flow through the external circuit. When charged, cobalt ions are oxidized
and lithium ions migrate into the graphite, when discharging the battery delivers energy to the
external load and when charging it recieves energy from a d.c. power source. The electrode
that acts as an anode, during discharging becomes a cathode when its charging.
Applications:
• Lithium-ion batteries are most commonly used in applications where one or more of
the advantages (size, weight or energy) outweigh the additional cost, such as mobile
telephones and mobile computing devices.
• Lithium-ion-polymer batteries are used when the battery design matters in a particular
application as different designs are possible (Cylindrical, jelly -roll design, flat
rectangular).
• It is used in current-generation laptops, cellular phones, video-recorders.
• It is also used in portable CD players, televisions and implantable medical devices.
Advantages:
➢ Lithium-ion batteries were designed to overcome the safety problems associated with
the highly reactive properties of Lithium metal.
➢ Long cycle life (400-1200 cycles).
➢ They are smaller, lighter and provide greater energy density than either nickel-
cadmium or nickel-metal-hydride batteries
➢ They can be operated in a wide temperature range and can be recharged before they
are fully charged.
➢ Typically designed to be recharged in the device rather than in an external charger.
34
 ➢ The average voltage of a Li-ion battery is equivalent to three Ni-Cd cells.
Disadvantages:
➢ Poor charge retention.
➢ The self discharge rate is about 10% per month.
➢ It prices are high compared to other types of cells commonly used.
1.7 Fuel cells
A fuel cell is a galvanic cell of a special type in which chemical energy contained in a fuel –
oxidant system is converted directly into electrical energy in a continuous electrochemical
process. It is an energy conversion device or electricity producer. The fuel cell has two
electrodes and an electrolyte like a primary cell. The reactants (i.e. fuel + oxidant) are
constantly supplied from outside and the products are removed at the same rate as they are
formed.
Cell: Fuel/ electrode/electrolyte/electrode/oxidant.
Anode: Fuel + oxygen ----------->Oxidation products+ ne-
Cathode: Oxidant + ne- ---------->Reduction products
A fuel cell consists of fuel, electrodes, electrolyte, & oxidant. Fuel undergoes oxidation at
the anode and oxidant gets reduced at the cathode. The cell can produce current as long as
the reactants are supplied. Most fuel cells produce low voltages, commonly less than one
volt, So a number of them are connected in series in “fuel batteries.”

Figure 1.7 Fuel cell

Eg:- H2-O2 fuel cell, CH 3 OH-O2 fuel cell, Solid-oxide fuel cell, Molten carbonate fuel cell
1.7.1 Advantages of fuel cells
• High fuel to electricity conversion efficiency of 70-75 % while a thermal power plant
converts 35-40% chemical energy of coal into electrical energy.
• Fuel cell products do not cause pollution problems such as noise pollution, chemical
pollution and thermal pollution normally associated with conversional power plants.

35
 • Fuel cell power plants can be located near the point of use electricity such as on an
urban location,rather than at a remote place. So transmission and distribution lose
(~30%) could be avoided.
• A fuel cell will produce a steady electric current as long as fresh reactants are
available.
1.7.2 Classification of fuel cells
S. No. Fuel cell type Electrolyte used
1 Polymer electrolyte Polymer membrane
2 Direct methanol Polymer membrane
3. Alkaline Potassium hydroxide
4. Phosphoric acid Phosphoric acid
5. Molten carbonate Lithium/potassium carbonate
6. Solid oxide Yittria stabilized zirconia

1.7.3 Alkaline fuel cell (AFC)

The hydrogen gas is continuously supplied at the anode and pure oxygen gas is continuously
supplied at the cathode form an external reservoir. The cell operates at about 80 o C and the
normal voltage is 1.10 V. At the anode, hydrogen is oxidized to the H + ions, which are
neutralized by the OH - ions of the electrolyte, forming water and electrons are released. At
the cathode, oxygen and water take electrons to form hydroxide ions. The overall reaction is
equivalent to the combustion of hydrogen. The only product discharge by the cell is water
vapor that escapes through the exhaust point. Note that the gases H 2 and O2 diffuse into the
electrode pores and so does the electrolyte solution.

Figure 1.7.3 AFC

Working:
At Anode:

36
 • H 2 (g) + 2OH -(aq) 2H 2 O(l) + 2e-
At Cathode:
1
• O2 (g) + H2 O(l) + 2e- 2OH -(aq)
2
1
Overall: H2+ O2 H2 O (l)
2
Advantages: Desirable attributes of the AFC include its excellent performance on hydrogen
(H2 ) and oxygen (O 2 ) compared to other candidate fuel cells due to its active O2 electrode
kinetics and its flexibility to use a wide range of electro-catalysts.
Disadvantages:
• The sensitivity of the electrolyte to CO 2 requires the use of highly pure oxidant and
fuel.
• As a consequence, the use of a reformer would require a highly effective CO and
CO2 removal system.
• If ambient air is used as the oxidant, the CO2 in the air must be removed. While this
is technically not challenging, it has a significant impact on the size and cost of the
system.
Applications: AFC is widely used in US space programs to produce electrical energy and
water onboard spacecraft.
1.7.5 Proton exchange membrane fuel cell (PEMFC)
Polymer electrolyte membrane fuel cells – also called proton exchange membrane fuel cells –
deliver high power density and offer the advantages of low weight and volume, compared to
other fuel cells. PEM fuel cells use a solid polymer as an electrolyte and porous carbon
electrodes containing a platinum catalyst. They need only hydrogen, oxygen from the air, and
water to operate and do not require corrosive fluids like some fuel cells. Polymer electrolyte
membrane fuel cells operate at relatively low temperatures, around 80 o C (176 o F).
Low temperature operation allows them to start quickly (less warm-up time) and results in
less wear on system components, resulting in better durability. However, it requires that a
noble-metal catalyst (typically platinum) be used to separate the hydrogen’s electrons and
protons, adding to system cost. The platinum catalyst is also extremely sensitive to CO
poisoning, making it necessary to employ an additional reaction to reduce CO in the fuel gas
if the hydrogen is derived from an alcohol or hydrocarbon fuel. This also adds cost.
Developers are currently exploring Pt/Ru catalysts that are more resistant to CO.
Role of Proton conducting membranes:

37
• The membrane function in two ways: It acts as the electrolyte which provides ionic
communication between the anode and the cathode and also it serves as the separator for
the two-reactant gases.
• Optimized proton and water transport properties of the membrane and proper water
management are crucial for efficient fuel cell operation.
• Dehydration of the membrane reduces the proton conductivity and excess of water can
lead to the flooding of the electrolyte. Both conditions result in poor performance.
• The absence of solution-phase electrolyte in PEF fuel cells, compared to alkaline and
phosphoric acid fuel cells greatly reduces the complexity of the fuel and oxidant flow
controls.
• Polymeric electrolyte is carbon dioxide tolerant.
• The most important breakthrough came with the development of perflourinated
membrane by DuPont. From 1966, the membrane requirements were best met by nafion
family of perfluorinated ionomer membranes. Lifetimes over 60,000 hrs have been
achieved at 353 K. Their general formula is

F F F F F F F F F

C C C C C C C C C

F F F F O F F F F

F C F

F C F

F C F

F C F
Construction: O=S=O

Electrolyte:-Ion exchange polymeric O

-
+
membranes. This is an excellent
H
insulator, but an excellent conductor of H + ions. The material used, consists of a
fluorocarbon polymer backbone, similar to Teflon, to which sulphonic acid groups are fixed
to the polymer and cannot leak out, but the protons of these groups are free to migrate
through the membrane.
Electrodes:-Typical gas diffusion electrodes, made up of porous C impregnated with Pt
catalyst. Noble metal treated carbon fiber paper/cloth which is directly bonded to the polymer
membrane at an elevated temperature and pressure (The catalytic electrode/membrane
configuration is referred to as membrane electrodes assemble, MEA).
Fuel:- Hydrogen

38
Oxidant:- Air
Catalyst:-Platinum
Interconnect:- Carbon or metal
Operating temperature:- 40 – 80 o C.
Charge-carrier:-H+
Electrode:-

Fig.1.7.5.1 schematic
of a typical PEMFC
electrode, which
displays three layers
(i) A Teflonized substrate (typically, carbon cloth)
(ii) A diffusion layer, generally formed by carbon particles of about 0.1 μm size with Teflon.
(iii) An active layer, where Pt catalyst grains are supported on carbon particles (Pt loading is
usually 0.4 mg/cm2 or less) with or without Teflon.
Cell reactions and Function of PEMFC:
PEM fuel cells operate at around 80 o C and practical efficiency of 60 %. Power output is in
the range of 5-200 KW. They are ideal for transportation and portable power. Additional
advantages are their high response, small size and low cost. A polymer electrolyte membrane
fuel cell is unusual in that its electrolyte consists of a layer of solid polymer which allows
protons to be transmitted from one fact to the other. Porous carbon is used as the anode and
cathode of the PEMFC, as shown in Fig. It basically requires H 2 and O 2 as its inputs, though
the oxidant may also be ambient air, and these gases must be humidified. It operates at a low
temperature because of the limitations imposed by the thermal properties of the membrane
itself. The operating temperatures are around 90 o C and a Pt catalyst is used.

39
Fig.1.7.5.2 PEMFC
At anode:
• H2 (g) 2H+(aq) + 2e-
At cathode
1
• O 2 (g) + 2H+(aq) + 2e- H2 O(l)
2
1
Overall reaction: H 2 (g) + O(g) H2 O(l)
2
Applications:
• PEM fuel cells are used primarily for transportation applications and some stationary
applications.
• Due to their fast startup time, low sensitivity to orientation, and favorable power-to-
weight ratio, PEM fuel cells are particularly suitable for use in passenger vehicles, such as
cars and buses.
Advantages:
The PEMFC has a solid electrolyte which provides excellent resistance to gas crossover.
The PEMFCs low operating temperature allows rapid start-up and, with the absence of
corrosive cell
constituents, the use of the exotic materials required in other fuel cell types, both in
stack construction.
PEMFCs are capable of high current densities of over 2 kW/I and 2 W/cm2 .
Disadvantages:
• The low and narrow operating temperature range makes thermal management
difficult, especially at very high current densities, and makes it difficult to use the
rejected heat for cogeneration.

40
 • Optimized proton and water transport properties of the membrane and proper water
management are crucial for efficient fuel cell operation. Dehydration of the membrane
reduces the proton conductivity and excess water can lead to the flooding of the
electrolyte. Both the conditions lead to poor performance.
• Perflourinated membranes have a high cost.
• PEMFCs are quite sensitive to poisoning by trace levels of contaminants including
CO, sulfur species and ammonia.
1.7.6 Differences between the fuel cell and galvanic cell:
Fuel Cell Galvanic Cell

1. They do not store chemical energy They store chemical energy

2. Reactants are fed from outside the cell The reactants from an integral part of its
continuously construction.
3. Need expensive noble metal catalysts & an These special conditions are not required
optimum to an operative for their efficient
functioning.
4. Do not get discharged and no need of Get-discharged when stored – up energy is
charging exhausted.
5. Such cells never become dead as long as Limited life span in use
fresh reactants are available
6. Useful for long-term electricity generation. Useful as portable power services.
7.Reaction products must be continuously No such problem
removed
8. No pollutants are generated (significant Pollutants are generated after their useful
environmental benefits) life
9. Produce power from fuels They cannot generate electricity from fuels
10. Significantly higher power densities Lower power density

1.8 Metal finishing

1.8.1 Introduction

Metal objects such as car components, kitchen utensils, juice cans, window frames, railings
and so on which we see in everyday life will have undergone a surface modification, referred
to as finishing. It covers a wide range of processes carried out to modify the surface

41
properties of a metal. The process involves deposition of a layer of another metal or a
polymer, conversion of a surface layer of atoms into oxide film or any other inorganic
compound film or any process which can finally improve the surface characteristics. Metal
finishing is done by electroplating, electroless plating, grinding wheels and honing, lapping
and burnishing tools to obtain a smooth surface of a component with desired characteristics.
Metal finishing is a process of electro deposition of an adherent metallic film of uniform
thickness on the surface of the substrate for the purpose of modifying its surface properties.
The metal finishing techniques were originally introduced in the industry for improving the
physical appearance of the metal objects by imbibing a decorative appeal. Since then a wide
range of technological developments in the field was taken place for imparting additional
desirable surface properties to the material other than their intrinsic properties to enhance the
utility of the metal. Some of them are
• Improving resistance to corrosion
• Enhancing resistance to chemical attack, abrasion and wear
• Imparting thermal resistance and resistance to impact
• Improving thermal and electrical properties
• Increasing hardness, thermal and optical reflectivity to the surface
• Making the surface resistant for moisture attack
1.8.2 Electroplating
The techniques of metal finishing include electroplating of metals and alloys and Electroless
plating of a modified surface. Electroplating is the process by which coating metal is
deposited on the base metal by passing a direct current through an electrolytic solution,
containing the soluble salt of the coating metal. It is primarily used for depositing a layer of
material to bestow a desired property (e.g., abrasion and wear resistance, corrosion protection
and aesthetic qualities) to a surface that otherwise lacks that property and sometimes to build
up thickness on undersized parts. The common metals used for coating purpose are Zn, Cu,
Ni, Cr, Ag, Au and Pt.
1.8.3 Theory of electroplating
Electroplating is the process of coating a metal on a substrate made up of another metal, alloy
or non-metal by the process of electrolysis. The process used in electroplating is called
electrodeposition and the principle is electrolysis. The electroplating device is an electrolytic
cell in which two electrodes (anode and cathode) are dipped in an electrolytic solution. The
part to be plated is the cathode of the circuit. In one technique, the anode is made of the
metal to be plated on the part. Both components are immersed in a solution called an

42
electrolyte containing one or more dissolved meal salts as well as other ions that permit the
flow of electricity. A rectifier supplies a direct current to the anode, oxidizing the metal
atoms that compromise it and allowing them to dissolve in the solution. At the cathode, the
dissolved metal ions in the electrolyte solution are reduced at the interface between the
solution and the cathode, such that they ‘plate out’ on to the cathode. The rate at which the
anode is dissolved is equal to the rate at which the cathode is plated, ie the current flowing
through the circuit. In this manner, the ions in the electrolyte bath are continuously
replenished by the anode. Other electroplating processes may use an inert anode such as lead
or graphite. In these techniques, ions of the metal to be plated must be periodically
replenished to maintain proper coating metal ion concentration in the bath. The device used
for electroplating is an electrolytic cell in the form of a tank having two electrodes immersed
in the electrolyte solution. The schematic representation of various components of the
electroplating unit is shown in Fig. 1.8.3.

Fig. 1.8.3 Schematic of the electroplating bath

Essential components include:
• An electroplating bath containing a conducting salt and the metal to be plated in a soluble
form as well as a buffer and additives.
• The article to be plated - electronically conducting cathode.
• The electronically conducting anode, the coating metal itself, or an inert material of good
electrical conductance like graphite.
• An inert vessel to contain the above mentioned materials made up of either rubber lined
steel, concrete or wood.
Suppose the anode is made of coating metal itself. During electrolysis, the concentration of
the electrolytic bath remains unaltered, since the metal ions deposited from the bath are

43
replenished continuously by the reaction of free anions with the anode metal. As an example,
if the CuSO 4 solution is used as an electrolyte, it ionizes as
CuSO 4 → Cu2+ + SO 4 2−
On passing current, Cu2+ ions go to the cathode and get deposited there.
• Cu2+ + 2e − → Cu
The free SO 4 2- ions migrate to the copper anode and dissolve an equivalent amount of copper
to form sulfate.
• Cu + SO 4 2- → CuSO 4 + 2e
Thus there is a continuous replenishment of electrolytic salt during electrolysis. If however,
the anode is made of some inert material like graphite, then electrolytic salt is added
continuously in order to maintain proper coating metal ion concentration in the bath.
Moreover the process of electroplating goes on nonstop, since the anode is not consumed and
its replacement is not required. The process involves the passage of current and electrolysis
of conducting media. Three important factors governing the electroplating process include
decomposition potential (E D), polarization and overvoltage.
1.8.3.1 Decomposition Potential (E D):
When an electric current is passed through the electrolyte solution the electrolysis starts and
the products formed, gather around the electrodes. Concentration in the vicinity of the
electrodes changes and a back emf sets in. e.g., in the electrolysis of water, if a small voltage
(~ 0.75V) is applied between two platinum electrodes immersed in the 1M sulphuric acid
solution, the electrolysis starts, proceeds to some extent and then decreases rapidly finally to
stop. The reason for this observation is the initial passage of current causing release of a
small amount of hydrogen and oxygen at the cathode and anode respectively. The gases are
adsorbed at the surface of electrodes and the inactive platinum electrode is converted into
active gas electrodes. This produces a back emf of the polarization current, which resists the
emf of the battery or applied voltage. At potential below 1.7V the back emf counterbalance
the effect of applied emf and the process of electrolysis is not sustained. If the applied voltage
is slowly increased, there is a slight increase in the current until the applied voltage just
exceeds the back emf (1.7 V), the current suddenly increases appreciably at that point. Thus,
the minimum external potential or voltage, at which the electrolysis current begins to increase
appreciably and continuous electrolysis sets in is known as decomposition potential of the
electrolyte. It is equal to back emf.
Measurement of decomposition potential (E D):
The schematic diagram for the determination of decomposition potential is shown in
Fig.1.8.4.1a The electrolytic cell consists of two platinum electrodes (E 1 and E2 ) dipped in

44
the electrolytic solution. The applied voltage (V) is measured at different resistance and the
corresponding current is measured with the help of milliammeter (M).

Fig. 1.8.3.1a Setup for measurement of decomposition potential

A series of readings for current passing through the electrolyte cell at corresponding applied
voltage is recorded and a graph is plotted to measure the electrode potential. A graph
between applied emf and the current density is shown in the following Fig.1.8.3.1b

Fig. 1.8.3.1b A graph of external voltage applied vs current density

The linear portions of the graph are extended, until they intersect. Voltage corresponding to
the point of intersection is the E D of the electrolyte.
Factors influencing decomposition potential:
Decomposition potentials of different electrolytes are different. Even the ED of an electrolyte
is not a constant. It depends upon the following factors;
• Strength of the current flowing through the cell
• Chemical nature of the electrodes
• Physical nature of the electrodes
• Activity of the electrolyte
• Absolute temperature.
Use of decomposition potential values:
45
• Knowledge of ED value enables the calculation of actual emf which is required for setting
in continuous electrolytic processes, electroplating and electrorefining.
• It helps in predicting the sequence of discharge process to occur.
• Used in the separation of a mixture of metal ions from a solution by electrolysis.
1.8.3.2 Overvoltage
The decomposition potential of an electrolyte is approximately equal to the emf of the
galvanic cell formed due to the discharge of products at the electrodes. The decomposition of
an electrolyte is therefore expected to start as soon as applied potential reaches the value of
reversible emf of the cell. This is true with respect to metal ions. But when products
discharged at the electrodes are gases, then the actual decomposition potential is invariably
much higher than its theoretical reversible electrode potential. The excess voltage is referred
to as overvoltage (η) of the gas. It may occur at both the electrodes.
Overvoltage (η) is the difference between the actual applied emf to bring about continuous
electrolysis and the theoretical emf needed for such electrolysis. For instance, the reversible
potential of oxygen gas with smooth Pt electrode is 1.23 V. But actual gas evolution takes
place at a potential of 1.68 V. The excess 0.45 V is the overvoltage of oxygen on smooth Pt
surface. The following factors influence the overvoltage of an electrolyte;
• Nature of the electrode surface (or material)
• Current density and temperature
• Nature of the electrolyte
Overvoltage is believed to be a surface phenomenon at the electrodes. Of the many steps
involved in gas evolution at electrodes, at least one is rather a slow process and requires
energy. The extra energy is supplied by the applied voltage and this extra energy is related to
overvoltage.
e.g., electrolysis of water

(i) H + (aq.) + e- H (fast)

(ii) H + H H2 (slow)
The step (ii) being slow, consumes energy and accounts for overvoltage. Hydrogen
overvoltage is the measure of the tendency of hydrogen to be liberated at the cathode. Higher
the value of overvoltage more difficult is the liberation of hydrogen on that metal.
1.8.3.3 Polarization
Since the electrolysis is a non spontaneous process, the minimum energy required to carry out
such a process is equal to the free energy increase accompanying the change. However, in
irreversible conditions, the potential to be applied for electrolysis is higher than the reversible

46
emf of the cell. A cell that requires excess voltage over the theoretical is said to be polarized
and the phenomenon is referred to as polarization. Electrolytic processes occur at the
electrodes of the cell. Polarization sets in the cell when the electrode processes become slow
and irreversible. Thus polarization in the cell is due to polarization at the electrodes.
Magnitude of overpotential is directly proportional to the extent of polarization. The observed
polarizations are of two types.
(a) Concentration polarization (b) Kinetic polarization
Concentration polarization:
An electrochemical reaction occurs only at the surface of the two electrodes. Reactant
concentration decreases in the electrolyte adjacent to the electrode surface. The reactant
species are transported to the electrode surface by processes like diffusion, migration and
convection from the bulk of the solution. When the rate of transport is insufficient to match
the rate of electrode reaction, current flowing through the cell drops. A higher potential than
the theoretical value is required to maintain the current at the necessary level. This
phenomenon is called concentration polarization. The steps involved in electrolytic processes
are
(i) Diffusion of reactant species towards the electrode and
(ii) Diffusion of product away from the electrode, cause concentration polarization.
Concentration polarization can be eliminated or at least minimized by increasing the
convection, by raising the temperature or mechanical agitation of the solution.
Kinetic or Activation polarization:
Activation polarization is caused when steps
i) Adsorption of the reactant on the electrode
ii) Charge transfer across the metal-solution interface and
iii) Desorption of the product from the electrode become slow and need activation
energy.
A higher potential than the theoretical value is to be applied to maintain current at the
necessary level. It is not possible to eliminate or minimize kinetic polarization by any means.
Activation polarization is normally very low, when metal deposition or metal dissolution i s
the electrode process. When the electrode process is a gas (H 2 and O2 ) evolution, kinetic or
activation polarization is usually very high.
Factors influencing polarization:
• Size and nature of the electrode
• Nature of ions accumulated on electrodes
• Electrolytic concentration
47
• Temperature
• Conductivity of electrolytic solution
• Stirring of electrolytic solution
• Use of depolarizer
Importance of polarization effect:
An impervious or non-porous film, contributes to the increase of polarization at an electrode.
Considerable polarization effect can also be seen where loosely adhering and even porous
films are formed. Such films either formed naturally (during manufacturing) or artificially
(by the application of special coatings or products of corrosion) are important in determining
the rate of corrosion of a metal or an alloy and also for the protection form corrosion.

1.8.4 Applications of electroplating

• Plating for aesthetic appearance:
• Plating for protection
• For electroforming
• Plating on non-metals

1.8.5 Characteristics of a good deposit

▪ The deposit should be bright and lustrous
▪ The deposit should be continuous, uniform, non porous and adhesive
▪ It should be hard and ductile
▪ It should be of fine grained nature

1.8.6 Factors influencing the nature of the deposit

There are several factors which affect the nature of an electro deposit.
(a) Current density
Higher the current density, more the deposition rate but will enforce the poor adhesion
and loose and brittle plating quality. There is the possibility of a burnt and spongy deposit.
Whereas low current density takes extra time to finish the job and is uneconomical.
Therefore, optimum moderate current densities should be applied.
(b) Metal ion concentration
As the electroplating involves the discharge of free metal ions, the concentration of free metal
ions plays an important role. If the concentration of metal ion is low the crystal size will be
smaller and a fine adherent film may be coated. Thus the ideal situation is low free metal ion
concentration in a concentrated solution of a metal compound which can be attained by
48
addition of a compound with a common ion or by the formation of complex compound and
ions. e.g., when copper is deposited from an electroplating bath containing copper sulphate
solution, sulphuric acid is added to increase the concentration of sulphate ion. The
concentration of cupric ions is reduced due to common ion effect.
(c) Temperature:
Generally, the solution to be deposited is used at room temperature. However, warm baths
are used for increasing solubility of electrolyte and current density. The size of the crystals
increases with increasing temperature and renders lower adherence. But on the other hand
the solubility and metal dissociation increase at higher temperature leading to the higher
conductance of the solution. Also, the mobility of ions increases at a higher temperature and
decreases the viscosity of the electrolyte solution so that the cathode film is replenished at a
faster rate. This increases the current density for a given voltage and reduces the tendency
towards treeing. There are disadvantages also of using high temperatures. Since, the
possibility of corrosion of equipment, decomposition of the organic addition agent and
evolution of hydrogen gas at cathode would increase at a higher temperature. So the
optimum range of temperature needs to be selected.
(d) pH of the electrolyte
The pH of the electrolyte solution should be properly maintained. The range of the pH varies
for different types of the plating bath. If pH is more towards the acidic side the nature of the
deposit will be affected adversely as the evolution of hydrogen gas is expected at cathode
thereby forming a burnt deposit. If pH is more towards the basic side the plating is delayed,
so uneven and thick deposit is obtained. Suitable buffers may be used for maintaining the
appropriate pH.
(e) Presence of additives:
To obtain electroplate with desire qualities and specifications, additional substances called
additives are added in small quantities to the electrolyte bath. These additives have the
capacity to modify the structure, appearance and characteristics of the deposit. The different
types of additives used are
(i) Complexing agents:
(ii) Brighteners:
(iii) Levellers:
(iv) Wetting agents:
(v) Structure modifiers:
(f) Throwing power of the plating bath

49
Throwing power is defined as the degree of uniformity of metal distribution or evenness of
deposit thickness obtained on a cathode of irregular shape. If the distribution of the deposit is
uniform throughout the surface of the article to be coated, the throwing power is considered
good.
1.8.7 Methods of cleaning the metal surface
It is essential to clean the surface of base metal before the application of the electroplated
coating. The common impurities found on the metal surface are grease, oil, oxide layer and
other extraneous matters. The following methods are employed to clean the metal surfaces.
(iii) Physical (Solvent) cleaning:- Physical cleaning is done with the help of solvents to
make the surface free from oil, grease, superficial dirt, and buffing, polishing and fatty
substances. The commonly used solvents such as chlorinated hydrocarbons, xylene, toluene,
aqueous cleaning agents are used with or without electric current. Solvent cleaning is made
more effective by vapour degreasing. An organic volatile solvent like trichloroethene is
heated and vapours are passed over the metal surface to be cleaned. The vapours condense
on the surface and condensed liquid dissolves and washes away the oil, grease and other
organic matter from the surface. The emulsifying agents are also added to the solvent to
remove organic impurities from the surface of the metal.
(ii) Chemical (Alkali) Cleaning: It is used to remove the minute residue of soil and grease
and for removal of tarnish and oxide film. The commonly used alkali cleaners consist of a
number of alkalies, soap, chelating agents like Na 2 O3 , sodium phosphates, NaOH etc. Alkali
cleaning is made more effective by passing current through a hot alkaline solution, with the
article to be cleaned constituting the cathode. The evolution of H 2 at the cathode and O2 at the
anode, metal helps to dislodge the greasy substance. It is followed by thorough rinsing with
water and then immersing in a very dilute solution of acids to remove traces of alkali after
cleaning is completed.
(iii) Mechanical Cleaning: Involves removal of the oxide layer (tarnish), loose rust and other
inorganic deposits from the surface to obtain better appearance, protection and optimum
effects. This is done by hand cleaning with bristle brush and some abrasives like sand papers,
polishing tools (grinding with grinding stone), scratch rubbing with chisel, knife, scrapers,
wire brush or a abrasive stone or paper and detergent.
(iv) Pickling: The oxides sometimes cannot be removed by simple alkali or mechanical
cleaning. The extraneous fragments like heavy scales of oxides, scratches and strains can be
removed from the surface by dissolving in the acid solution. The acid pickling involves the
removal of such oxides; rust or tarnish by immersing the material (except Al) in acid like dil.
HCl or dil.H 2 SO4 or dil. HNO3 . Pickling of Al is done in alkaline solution, whereas pickling

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of Cu, Ni or brass articles are accomplished in a solution of dil. HNO3 or a mixture of dil.
HNO 3 and dil. H 2 SO4 . Pickling is usually followed by polishing and buffing.
(v) Electro polishing :- In this method, the metal to be cleaned is made anode in a suitable
solution. During the process, a surface layer of the metal gets dissolved along with the
impurities. It also helps to remove minor surface irregularities. The most commonly used
baths for electro polishing contain sulphuric acid, phosphoric acid, chromic acid, nitric acid
etc. After the process, the metal is thoroughly rinsed with water, dried and used for
electroplating.
1.8.8 Electroplating of chromium
Chromium plating is a finishing treatment utilizing the electrodeposition of a thin layer of
chromium on a metal object. This layer can be decorative or corrosion protective to the base
surface. The process of chromium plating includes degreasing to remove heavy soiling,
manual cleaning to remove all residual traces of dirt and surface contamination and various
pretreatments depending on the objectives of the coating. Different etching solutions such as
hydrochloric, hydrofluoric, sulphuric acid and ferric chloride are used. Further, the treated
base material is placed into the chrome plating bath for electroplating of desired thickness.
• Chromium coatings are generally thinner and have micro pores in it. As the thickness of
the coating increases, cracks develop in the coatings. Hence, chromium coatings are
always plated on nickel/copper undercoates. Ni gives protection and chromium gives a
decorative finish.
• Chromium anodes are not used in electroplating of chromium on account of two
difficulties. These electrodes become passive in acidic medium and they result in a black
deposit.
• Chromium has higher electrode potential and can be easily coated on the iron to protect
from rusting/corrosion
• The anode efficiency is nearly 100 % whereas cathode efficiency is at best around 20 %.
It may be inferred that metal going into the solution is five times of the metal getting
deposited, resulting in building up of excessive chromic acid concentration. This disturbs
the ratio of Cr(III) to Cr(VI) and the conductivity of the bath and dull deposits called
burnt deposits are obtained. To avoid this, inert material is used as anode and chromium
electrolyte in the bath.

Table 1.8.8 Comparison of decorative and hard coating of chromium

Decorative coating Hard coating
Bath Chromic acid (250 g) + Chromic acid (250 g) +

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 composition H2 SO4 (2.5 g) + H2 SO4 (2.5 g) +
Trivalent chromium (1g) Trivalent chromium (1
g)
Operating 45 – 55 °C 45 – 55 °C
Temperature
Anode Insoluble anodes like Lead – lead : 6%
Pb – Pb : 6% Sb – Pb: 7%
Sb - Pb--7% Sn
Sn
Cathode Article to be coated Article to be coated
Current density 145--430 A/ft 2 290--580 A/ft 2
Cathode 10 – 15 17 – 21
efficiency
Applications Decorative applications with Coating of industrial
corrosion resistance finish on components like gauges,
cycles, automobiles, dies, cutting tools,
furniture, household fittings, piston rings and
aircraft, surgical and dental hydraulic rams.
instruments.

1.8.9 Electroless plating

Electroless plating is a method of depositing a metal film on a substrate surface (conductor or

non-conductor) from metal salt solution using a suitable reducing agent without using
electrical energy. The reaction can be depicted as
Metal ions + Reducing agent Metal + Oxidized product
The method involves the deposition of metals such as Cu, Ag, Ni, Au or Pd on the surface of
the base material by means of a reducing agent. Electroless plating results in a fine grained
metal deposit that has similar finishing as that of traditional electrodeposit finishing. In
industries, such process is used for plating on non-conductors like plastic, electroformed dies,
hard memory disks, printed circuit boards (PCBs) or to obtain an extremely uniform plate.
This technique is also used for the prevention of corrosion.
Process of electroless plating: The process of electroless plating involves the following
steps:

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(i) Preparation of active surface: This is the most important step and the surface is activated by
any of the following ways.
(a) etching – by acid treatment
(b) electroplating with a thin layer of metal or insulators like plastic surfaces f ollowed by heat
treatment
(c) Alternate treatment with SnCl2 and PdCl2 on the plastic surface
SnCl2 + PdCl2 Pd + SnCl4
Pd is coated on plastic.
(ii) Preparation of plating bath:
(a) Metal to be coated in the form of chloride or sulphate solution
(b) Reducing agents like formaldehyde and sodium hypophosphate for reduction of metal ion
to metal
(c) Complexing agents like EDTA, tartrates, citrates to form metal complexes to prevent
excess deposition
(d) Stabilizers like thiourea, calcium ions too prevent decomposition of the bath and to impart
stability to the solution
(e) Exaltants (accelerators) like succinates, glycinates and fluorides to increase the rate of
plating
(f) Brighteners like thiosulphate to give a lustrous appearance
(g) Buffers like boric acid to maintain the pH
(iii) Reduction step: Active surface is dipped in the bath and deposition is carried out. The
plating is carried out in a series of tanks where the object is immersed to plate the desired
metal. The rate of deposition is controlled by the amount of reducing agent present and the
type of chelating agent used. The deposition rate is normally 12.5 – 25 µm, although, it has
been done up to 650 µm in thickness.
Advantages of electroless plating
The following are main advantages of electroless plating
• More uniform coating on the surface of object whatever shape it may have. Even the
objects having irregular shapes, holes, recesses, internal surfaces, valves or threaded
parts get uniform deposit since it has better throwing power than electroplating.
• Electrical power and other accessories are not required.
• Coating is harder than regular plating and better wear resistance.
• Deposits have compatible wettability for oils, inherent lubricity and non-galling
characteristics, unlike electrolytic nickel.

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 • Deposits are much superior to electroplated nickel and hard chrome, as they are less
porous and provide better corrosion protection to steel substrates.
• Electroless plating of Ni on aluminum substrate enhances the solderability together
with providing a non-magnetic under lay in magnetic components. The deposits are
less porous and possess unique characteristic chemical, mechanical and magnetic
properties.
• Additives or levelers are not required in the process nor the complex filtaration
method requirement.
• It is a simple process, so requires simple equipment.
Disadvantages of electroless plating
The main disadvantages of the process are the following;
• Due to speedy chemical renewal, cost of waste treatment is high.
• The frequency of dumping electroless bath is high as it is sensitive to contamination
• Costs per unit weight of the deposited metal are more.
• It needs pure chemicals.
• Chemical reductants are more expensive than electricity.
• Metal salts and reductant used in electroless plating solutions are thermodynamically
not stable.
• Impurities or dust or colloidal matter (even if present in trace amount) promote the
decomposition of bath components.
1.8.9.1 Electroless plating of Copper
It is an auto-catalytic reaction used to deposit a coating of electroless copper on a substrate
without the use of electrical energy. It is commonly used to plate plastic for decorative
purposes and parts for engineering applications, particularly to render conductivity for
electronic and printed circuit boards.
Reducing agents generally react with the plating bath, resulting in slow, deposition rates and
poor deposit quality. It can be prevented by rejuvenating the bath at regular intervals. The
bath solution undergoes spontaneous decomposition, resulting in an additional waste stream
of copper and etching solution as copper built up on the tanks from the bath solution, must be
stripped with an etchant such as sulphuric acid and hydrogen peroxide.
Electroless plating bath for copper includes;
• Coating solution : CuSO 4 soln
• Reducing agent : HCHO
• Buffer: NaOH & Rochelle salt

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 • Complexing agent: EDTA di sodium salt
• Optimum pH: 11
• Optimum temperature: 25 °C
The reactions involved at two electrodes are
At cathode:
• Cu2+ (aq) + 2e- Cu (S)
At anode:
• 2HCHO + 4OH -(aq.) 2HCOO -(aq.) + 2H2 O (l) + H2 (g) + 2e-
Overall reaction:
Cu2+(aq.) + 2HCHO + 4OH -(aq.) 2HCOO -(aq.) + 2H 2 O(l) + H2 (g)
Since Cu2+ ions and HCHO are consumed during the redox reaction, these are replenished
periodically. The redox reaction involves consumption of hydroxyl ions and pH of the
solution decreases as the reaction progresses. Hence addition of buffer is essential. Usual
plating rate is 1-5 µmh-1 .
Applications of electroless plating:
• Electroless copper plating is widely used for metalizing printed circuit boards (PCBs)
• It is used as a base coating for subsequent conventional electroplating
• It is used for producing through hole connections and for decorative plating on
plastics. When double sided PCBs are fabricated then holes are drilled for making
electrical connections. These holes are plated by electroless plating.

1.8.10 Comparison of electroplating and electroless plating

Table 1.8.9 Comparison of electroplating and electroless plating
Property Electroplating Electroless plating
Driving force Electric current Autocatalytic redox
reaction
Anode reaction
Cathode Article to be plated Article to be plated with a
catalytic surface
Anode Separate anode Article to be plated
Reducing agent Electrons bring about Chemical reagents bring
about reduction reaction
Anode reactant M or H2 O R, the reducing agent in
solution

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Nature of deposit Pure metal or alloy Usually metal
contaminated with species
derived from the redox
reaction
Thickness limit 1 - 100 1 – 100
(µm)
Applicability Applicable to Can be used for conductors
conductors only and non-conductors
Throwing power Less throwing power; More throwing power and
cannot be used for can be used for irregular
irregular shapes and and uneven shaped objects
intricate parts

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