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Half reactions can be written to describe both the metal undergoing oxidation (known as the anode) and the metal undergoing reduction (known as the cathode). Half reactions are often used as a method of balancing redox reactions. For oxidation-reduction reactions in acidic conditions, after balancing the atoms and oxidation numbers, one will ...
The increase in the oxidation state of an atom, through a chemical reaction, is known as oxidation; a decrease in oxidation state is known as a reduction. Such reactions involve the formal transfer of electrons: a net gain in electrons being a reduction, and a net loss of electrons being oxidation. For pure elements, the oxidation state is zero.
At chemical equilibrium, the reaction quotient Q r of the product activity (a Red) by the reagent activity (a Ox) is equal to the equilibrium constant (K) of the half-reaction and in the absence of driving force (ΔG = 0) the potential (E red) also becomes nul. The numerically simplified form of the Nernst equation is expressed as:
At the positively charged anode, an oxidation reaction occurs, generating oxygen gas and giving electrons to the anode to complete the circuit. The two half-reactions, reduction and oxidation, are coupled to form a balanced system. In order to balance each half-reaction, the water needs to be acidic or basic.
The electric potential also varies with temperature, concentration and pressure. Since the oxidation potential of a half-reaction is the negative of the reduction potential in a redox reaction, it is sufficient to calculate either one of the potentials. Therefore, standard electrode potential is commonly written as standard reduction potential.
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Electrode potentials of successive elementary half-reactions cannot be directly added. However, the corresponding Gibbs free energy changes (∆G°) must satisfy ∆G° = – z FE°, where z electrons are transferred, and the Faraday constant F is the conversion factor describing Coulombs transferred per mole electrons. Those Gibbs free energy ...
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