Chapter 1. Introduction of Electrochemical Chapter 1. Introduction of Electrochemical Concepts Concepts

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Chapter 1. Introduction of Electrochemical Chapter 1. Introduction of

Electrochemical Concepts Concepts
Chapter · January 2020
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Chapter 1. Introduction of Electrochemical
Concepts
• Electrochemistry – concerned with the interrelation of

electrical and chemical effects. Reactions involving the
reactant – the electron.
Chemical changes caused by the passage of current
• An electrochemical system is not homogeneous but is

heterogeneous.
• Broad Field : electroanalysis, sensors, energy storage

and conversion devices, corrosion, electrosynthesis, and
metal electroplating.
Electroanalytical Chemistry
• Electroanalytical chemistry encompasses a group of

quantitative analytical methods that are based upon the
electrical properties of an analyte solution when it is
made part of an electrochemical cell.
• These methods make possible the determination of a
particular oxidation state of an element.
Ox + ne- ↔ Red
• There are two general types of electrochemical methods:

potentiometric (no current, equilibrium potential) and
voltammetric (current measured as a function of the
applied potential.
Electrochemical Cells
Electrochemical cells consist of two electrodes: an anode

(the electrode at which the oxidation reaction occurs) and a
cathode (the electrode at which the reduction reaction
occurs).
Cu(s) + Zn+2 ↔ Cu+2 + Zn(s)
Cu(s) ↔ Cu+2 + 2e- (oxidation)
Zn+2 + 2e- ↔ Zn(s) (reduction)
There are two types of electrochemical cells: galvanic

(ones that spontaneously produce electrical energy) and
electrolytic (ones that consume electrical energy).
Conduction
1. Metals
2. Solution (ion
migration)
3. Electrode rxns
(at interfaces)
A potential difference between two electrodes represents a

tendency for the reaction to occur.
Electrochemical Potentials
The potential that develops in a cell is a measure of the

tendency for a reaction to proceed toward equilibrium.
2.303 RT log [Ox]

E= Eo´ +
nF [Red]
Measured
E vs. Ref Nernst Equation
ax = γ [x]
Standard reduction reactions: all relative

to the H2/H+ reaction, 298 K, unit activities
for all species, and pH 0.
Electrochemical Potentials
We use concentrations in the Nernst equation, but really

activities are the proper term. The activity of a species can
be defined as the ability of a species to participate an
equilibrium reaction involving itself.
e.g. Fe+3 + e- ↔ Fe+2 FeCl+2, etc.

Depends on ionic strength
Ecell = Ecathode – Eanode
∆Grxn = - nFEcell Key equations
∆Grxn = -RTlnKeq
Reference Electrodes
All cell potential measurements require two electrodes!
1. AgCl(s) + e- ↔ Ag(s) + Cl-
E = Eo + (0.059/n)log1/[Cl-]
2. Hg2Cl2(s) + 2e- ↔ 2Cl- + 2Hg(l)
E = Eo + (0.059/2)log1/[Cl-]2
n = number of electrons transferred per mole, 2.303 RT/F = 0.059 V

Cu+2 + H2(g) ↔ Cu(s) + 2H+
Zn/ZnSO4 (aZn+2 = 1.00)//CuSO4 (aCu+2 = 1.00)/Cu

Anode (oxidation) Cathode (reduction)
This shorthand is not always used in your textbook.
Electrochemical Cells and Reactions
Electrode (conductor) – Electrolyte (ionic solution)

Electrode Solution
solid solution Ox
e-
Red
Electrodes: Pt, Au, Pd, C, Hg
Ox + e- Red
Electrolyte solutions (low ohmic resistance):

ionic solutions (NaCl), molten salts, and
ionic polymers (Nafion).
Electrode reaction kinetics are affected by the electrode

surface cleanliness, surface microstructure, and surface
chemistry.
Two electrified interfaces but only one of interest.
V = J/C measure of the

energy available to drive
charge externally between
electrodes.
Rate of oxidation = Rate of reduction
Reference electrode: AgBr + e- Ag + Br-(aq) E0 = 0.071V

vs. NHE
Magnitude of the
potential controls the
direction and rate of
charge transfer.
As a potential is moved
negative, the species
that will be reduced
first (assuming all are
rapid) is the oxidant
(acceptor) in the couple
with the least negative
Eo.
• There are two types of current flow:
1. Faradaic – charge tranferred across the electrified

interface as a result of an electrochemical reaction.
dQ = i = nF dN
Q = nFN
dt dt
2. Non-faradaic – charge associated with movement

of electrolyte ions, reorientation of solvent dipoles,
adsorption/desorption, etc. at the electrode-electrolyte
interface. This is the background current in
voltammetric measurements.
Pt/H+, Br- (1M)/AgBr/Ag
(+) current = cathodic

(-) current = anodic
(+) potential = left
(-) potential = right
Br2 + 2e- 2Br- E0 = 1.09 V vs. NHE

2H+ + 2e- H2 E0= 0.00 V vs. NHE
Ecell = Ec - Ea
Hg/H+, Br- (1M)/AgBr/Ag

Kinetically fast reactions have
significant faradaic current
flow near Eo, while sluggish
reactions have little current
flow except at large
overpotentials.
Hg2Br2 + 2e- 2Hg + 2Br- E0 = 0.14 V vs. NHE

2H+ + 2e- H2 E0= 0.00 V vs. NHE
Hg/H+, Br- (1M), Cd+2(1mM)/AgBr/Ag
CdBr42- + 2e- Cd(Hg) + 4Br-
Hg2Br2 + 2e- 2Hg + 2Br- E0 = 0.14 V vs. NHE

2H+ + 2e- H2 E0= 0.00 V vs. NHE
Electrified Interfaces
Ideally polarizable electrode (IPE) – no charge transfer

across the interface. Ions move in and out of the interfacial
region in response to potential changes. The interface
behaves as a capacitor (charge storage device).
Excess electrons on one

plate and a deficiency on
the other.
Changing the potential, E, causes the charge stored, Q,

to change according to the relationship:
Q(coulombs) = C(farads) x E(volts)

qmetal = -qsolution charge neutrality!
Compact Layer = inner and outer Helmholtz planes

(electrostatic forces are very strong!)
Diffuse Layer = gradient of charge accumulation

(thermal agitation)
σmetal = qmetal/area (µC/cm2)
The excess charge on a metal is confined to the near surface region.

However, the balancing charge on the solution side of the interface
extends out into the solution with some thickness. (ionic zones in sol.)
σmetal = -(σIHP + σOHP + σdiffuse)

Structure of the electric double layer has
a major effect on electrode reaction
kinetics! (Faradaic reaction rates).
Species not specifically adsorbed

approach the OHP.
Φ2 – Φs is wasted!!
Φm – Φs is potential felt by analyte
⎛ dy ⎞
Field strength ⎜⎝ dx ⎟⎠ x = x 2 is critical!!
The solution side of the interface consists of a compact

layer (inner and outer Helmholtz layers) plus a diffuse layer.
Diffuse layer extends from the OHP to the bulk solution.

Ionic distribution influenced by ordering due to coulombic
forces and disorder caused by random thermal motion.
Qm + (QCL + QDL) = 0 Qm = - (QCL + QDL)
Q = CE (C = Farad E = voltage difference)

QDL = CdlA(E-Epzc) (A = area (cm2) Epzc = point of zero charge)
1/CTOT = 1/CCL + 1/CDL Smallest value dominates

the interfacial capacitance
CCL CDL
Electrochemical Experiment and Variables in
Electrode pretreatment matters a great deal!!!

1. Mass transfer of
reactant/product to and away
from the electrode interface.
2. Electron transfer at interface.
3. Preceeding or follow-up
chemical reactions.
4. Surface processes
(adsorption/desorption)
Working Electrode (Indicator Electrode)

η = E - Eeq
dQ
i (amperes) = (coulombs/s)
dt
Q (coulombs)
= N (moles electrolyzed)
nF (coulombs/mol)
dN i i
Rate (mol/s) = = Rate (mol/s-cm2) =
dt nF nFA
Mass Transport
Modes of Mass Transport

1. Migration – movement of
charged body under
influence of an electric field.
2. Diffusion – movement of
species under the influence
of a concentration gradient.
3. Convection - stirring or
hydrodynamic transport.
dCi(x) ziF dΦ(x)

Ji(x) = -Di - DiCi - Ciυ(x)
dx RT dx
Ji(x) = flux of I (mol/s-cm2) D = diffusion coeff. (cm2/s) C = conc. (mol/cm3)

dΦ(x)
= potential gradient z = charge on species υ(x) = velocity (cm/s)
dx
Mass Transport
l = (2Dt)1/2
Diffusion layer thickness
υmt = Do (dCo/dx)x=0
υmt = Do (C*o – Co(x=0))/δo
Do (C*o – Co(x=0))/δo = i/nFA = Dr(Cr(x=0) – C*r)/δr

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Chapter 1. Introduction of Electrochemical Chapter 1. Introduction of

Chapter · January 2020

Nisreen Kais Abood

determination of cefixime View project

The user has requested enhancement of the downloaded file.

• Electrochemistry – concerned with the interrelation of

Chemical changes caused by the passage of current

• An electrochemical system is not homogeneous but is

• Broad Field : electroanalysis, sensors, energy storage

• Electroanalytical chemistry encompasses a group of

• There are two general types of electrochemical methods:

Electrochemical cells consist of two electrodes: an anode

Cu(s) + Zn+2 ↔ Cu+2 + Zn(s)

Cu(s) ↔ Cu+2 + 2e- (oxidation)

Zn+2 + 2e- ↔ Zn(s) (reduction)

There are two types of electrochemical cells: galvanic

A potential difference between two electrodes represents a

The potential that develops in a cell is a measure of the

2.303 RT log [Ox]

Standard reduction reactions: all relative

We use concentrations in the Nernst equation, but really

e.g. Fe+3 + e- ↔ Fe+2 FeCl+2, etc.

Ecell = Ecathode – Eanode

∆Grxn = - nFEcell Key equations

2. Hg2Cl2(s) + 2e- ↔ 2Cl- + 2Hg(l)

n = number of electrons transferred per mole, 2.303 RT/F = 0.059 V

Cu+2 + H2(g) ↔ Cu(s) + 2H+

Zn/ZnSO4 (aZn+2 = 1.00)//CuSO4 (aCu+2 = 1.00)/Cu

Electrode (conductor) – Electrolyte (ionic solution)

Electrolyte solutions (low ohmic resistance):

Electrode reaction kinetics are affected by the electrode

Two electrified interfaces but only one of interest.

V = J/C measure of the

Rate of oxidation = Rate of reduction

Reference electrode: AgBr + e- Ag + Br-(aq) E0 = 0.071V

• There are two types of current flow:

1. Faradaic – charge tranferred across the electrified

2. Non-faradaic – charge associated with movement

Pt/H+, Br- (1M)/AgBr/Ag

(+) current = cathodic

Br2 + 2e- 2Br- E0 = 1.09 V vs. NHE

Hg/H+, Br- (1M)/AgBr/Ag

Hg2Br2 + 2e- 2Hg + 2Br- E0 = 0.14 V vs. NHE

Hg/H+, Br- (1M), Cd+2(1mM)/AgBr/Ag

CdBr42- + 2e- Cd(Hg) + 4Br-

Hg2Br2 + 2e- 2Hg + 2Br- E0 = 0.14 V vs. NHE

Ideally polarizable electrode (IPE) – no charge transfer

Excess electrons on one

Changing the potential, E, causes the charge stored, Q,

Q(coulombs) = C(farads) x E(volts)

qmetal = -qsolution charge neutrality!

Compact Layer = inner and outer Helmholtz planes

Diffuse Layer = gradient of charge accumulation

σmetal = qmetal/area (µC/cm2)

The excess charge on a metal is confined to the near surface region.

σmetal = -(σIHP + σOHP + σdiffuse)

Species not specifically adsorbed

Φm – Φs is potential felt by analyte

Do (Co – Co(x=0))/δo = i/nFA = Dr(Cr(x=0) – Cr)/δr