Electrochemistry
The study of chemical processes that involve the transfer of electrons, encompassing both spontaneous redox reactions (galvanic cells) and non-spontaneous reactions driven by electrical energy (electrolysis).
Redox Reactions
Oxidation and reduction always occur together in redox reactions:
- Oxidation: Loss of electrons, increase in oxidation number
- Reduction: Gain of electrons, decrease in oxidation number
- Oxidising agent: Species that is reduced (gains electrons)
- Reducing agent: Species that is oxidised (loses electrons)
Electrochemical Cells
Galvanic (Voltaic) Cells
Spontaneous cells that produce electrical energy from chemical reactions:
- Anode: Site of oxidation (negative electrode, electrons flow out)
- Cathode: Site of reduction (positive electrode, electrons flow in)
- Electrons flow from anode to cathode through external circuit
- Current flows from cathode to anode (opposite direction)
- Salt bridge: Maintains electrical neutrality by allowing ion flow between half-cells
Electrolytic Cells
Non-spontaneous cells that use electrical energy to drive chemical reactions:
- External power source forces electron flow
- Anode: positive terminal (oxidation)
- Cathode: negative terminal (reduction)
Cell Notation (Cell Diagram)
Standard notation for representing electrochemical cells:
$$ \text{Anode} \mid \text{Anode electrolyte} \parallel \text{Cathode electrolyte} \mid \text{Cathode} $$
- Single vertical line (|) represents phase boundary
- Double vertical line (||) represents salt bridge
- Inert electrodes (Pt, graphite) used when no solid metal participates
Examples:
- $\text{Zn}(s) \mid \text{Zn}^{2+}(aq) \parallel \text{Cu}^{2+}(aq) \mid \text{Cu}(s)$
- $\text{Pt}(s) \mid \text{Br}^-(aq), \text{Br}_2(l) \parallel \text{Cl}_2(g), \text{Cl}^-(aq) \mid \text{Pt}(s)$
BrBr
ClCl
Standard Electrode Potential (E°)
The potential of a half-cell under standard conditions (1 M solutions, 1 atm gases, 25°C).
Standard Hydrogen Electrode (SHE)
Reference electrode with $E° = 0.00$ V: $2\text{H}^+(aq) + 2e^- \rightarrow \text{H}_2(g)$
[H][H]
Standard Cell Potential (E°cell)
$$ E°_{cell} = E°_{cathode} - E°_{anode} $$
- Positive $E°_{cell}$ indicates spontaneous reaction
- More positive cathode: stronger oxidising agent
- More negative anode: stronger reducing agent
Electromotive Force (EMF) and Gibbs Free Energy
$$ \Delta G° = -nFE°_{cell} $$
Where:
- $n$ = number of electrons transferred
- $F$ = Faraday constant (96,485 C/mol)
- Negative $\Delta G°$ = spontaneous reaction
Nernst Equation
Relates cell potential to concentration:
$$ E_{cell} = E°_{cell} - \frac{RT}{nF} \ln Q $$
At 25°C:
$$ E_{cell} = E°_{cell} - \frac{0.0592}{n} \log Q $$
Electrolysis and Faraday's Laws
Faraday's First Law: Mass of substance produced is proportional to quantity of electricity passed.
Faraday's Second Law: Masses of different substances produced by the same quantity of electricity are proportional to their equivalent weights.
$$ m = \frac{Q \times M}{n \times F} $$
Where:
- $m$ = mass of substance produced
- $Q$ = charge passed (current × time)
- $M$ = molar mass
- $n$ = number of electrons per ion
- $F$ = Faraday constant
Applications
- Batteries: Lead-acid, alkaline, lithium-ion
- Fuel cells: Hydrogen-oxygen fuel cells
- Corrosion: Rusting as electrochemical process
- Electroplating: Coating metals using electrolysis
Related Pages
- FAD1018 - Basic Chemistry II — course page
- Redox Reactions — oxidation-reduction fundamentals
- Thermodynamics — Gibbs free energy relationships
Sources
- L1 L2 Electrochemistry — Lectures 1-2 on electrochemical cells (redox, cell notation, standard potential)
- Electrochemistry Part 2 — Lecture part 2 on driving force, Nernst equation, equilibrium
- FAD1018 L4-L5 — Electrolytic Cell — Electrolysis, selective discharge, overpotential, industrial cells
- FAD1018 Tutorial 4 — Electrochemistry — tutorial practice