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This gives the SCE a potential of +0.248 V vs. SHE at 20 °C and +0.244 V vs. SHE at 25 °C, [1] but slightly higher when the chloride solution is less than saturated. For example, a 3.5M KCl electrolyte solution has an increased reference potential of +0.250 V vs. SHE at 25°C while a 1 M solution has a +0.283 V potential at the same temperature.
The overall chemical reaction taking place in a cell is made up of two independent half-reactions, which describe chemical changes at the two electrodes. To focus on the reaction at the working electrode , the reference electrode is standardized with constant (buffered or saturated) concentrations of each participant of the redox reaction.
During the early development of electrochemistry, researchers used the normal hydrogen electrode as their standard for zero potential. This was convenient because it could actually be constructed by "[immersing] a platinum electrode into a solution of 1 N strong acid and [bubbling] hydrogen gas through the solution at about 1 atm pressure".
According to a more specific definition presented by Trasatti, [2] the absolute electrode potential is the difference in electronic energy between a point inside the metal (Fermi level) of an electrode and a point outside the electrolyte in which the electrode is submerged (an electron at rest in vacuum).
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The data below tabulates standard electrode potentials (E°), in volts relative to the standard hydrogen electrode (SHE), at: Temperature 298.15 K (25.00 °C; 77.00 °F); Effective concentration (activity) 1 mol/L for each aqueous or amalgamated (mercury-alloyed) species; Unit activity for each solvent and pure solid or liquid species; and
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