The data below tabulates standard electrode potentials (E°), in volts relative to the standard hydrogen electrode (SHE), at:
Variations from these ideal conditions affect measured voltage via the Nernst equation.
Electrode potentials of successive elementary half-reactions cannot be directly added. However, the corresponding Gibbs free energy changes (∆G°) must satisfy
where z electrons are transferred, and the Faraday constant F is the conversion factor describing Coulombs transferred per mole electrons. Those Gibbs free energy changes can be added.
For example, from Fe2+ + 2 e− ⇌ Fe(s) (–0.44 V), the energy to form one neutral atom of Fe(s) from one Fe2+ ion and two electrons is 2 × 0.44 eV = 0.88 eV, or 84 907 J/(mol e−). That value is also the standard formation energy (∆Gf°) for an Fe2+ ion, since e− and Fe(s) both have zero formation energy.
Data from different sources may cause table inconsistencies. For example: Cu + + e − ⇌ Cu ( s ) E 1 = + 0.520 V Cu 2 + + 2 e − ⇌ Cu ( s ) E 2 = + 0.337 V Cu 2 + + e − ⇌ Cu + E 3 = + 0.159 V {\displaystyle {\begin{alignedat}{4}&{\ce {Cu+ + e-}}&{}\rightleftharpoons {}&{\ce {Cu(s)}}&\quad \quad E_{1}=+0.520{\text{ V}}\\&{\ce {Cu^2+ + 2e-}}&{}\rightleftharpoons {}&{\ce {Cu(s)}}&\quad \quad E_{2}=+0.337{\text{ V}}\\&{\ce {Cu^2+ + e-}}&{}\rightleftharpoons {}&{\ce {Cu+}}&\quad \quad E_{3}=+0.159{\text{ V}}\end{alignedat}}} From additivity of Gibbs energies, one must have 2 ⋅ E 2 = 1 ⋅ E 1 + 1 ⋅ E 3 {\displaystyle 2\cdot E_{2}=1\cdot E_{1}+1\cdot E_{3}} But that equation does not hold exactly with the cited values.