Unit activity for each solvent and pure solid or liquid species; and
Absolute partial pressure 101.325 kPa (1.00000 atm; 1.01325 bar) for each gaseous reagent — the convention in most literature data but not the current standard state (100 kPa).
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
∆G° = –zFE°,
where z electrons are transferred, and the Faraday constantF is the conversion factor describing Coulombs transferred per mole electrons. Those Gibbs free energy changes can be added.
For example, from Fe2+ + 2e− ⇌ 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: From additivity of Gibbs energies, one must have But that equation does not hold exactly with the cited values.
Table of standard electrode potentials
Legend: (s) – solid; (l) – liquid; (g) – gas; (aq) – aqueous (default for all charged species); (Hg) – amalgam; bold – water electrolysis equations.
^ abNot specified in the indicated reference, but assumed due to the difference between the value −0.454 and that computed by (2×(−0.499) + (−0.508))/3 = −0.502, exactly matching the difference between the values for white (−0.063) and red (−0.111) phosphorus in equilibrium with PH3.
^ abcdefghijklLee, J. L. (1983) [1977]. A New Concise Inorganic Chemistry (3rd ed.). London / Wokingham, Berkshire: English Language Book Society & Van Nostrand Reinhold (UK). p. 107. ISBN0-442-30179-0. OL4079768W – via the Internet Archive.
^Pourbaix, Marcel (1966). Atlas of Electrochemical Equilibria in Aqueous Solutions. Houston, Texas; Cebelcor, Brussels: NACE International. OCLC475102548.
^ abcLavrukhina, Avgusta Konstantinovna; Pozdni︠a︡kov, Aleksandr Aleksandrovich (1970). Analytical chemistry of technetium, promethium, astatine and francium. Ann Arbor: Ann Arbor-Humphrey Science Publishers. p. 237. ISBN0-250-39923-7. OCLC186926.
^Rock, Peter A. (February 1966). "The Standard Oxidation Potential of the Ferrocyanide-Ferricyanide Electrode at 25° and the Entropy of Ferrocyanide Ion". The Journal of Physical Chemistry. 70 (2): 576–580. doi:10.1021/j100874a042. ISSN0022-3654.
^Pavlishchuk, Vitaly V.; Addison, Anthony W. (January 2000). "Conversion constants for redox potentials measured versus different reference electrodes in acetonitrile solutions at 25°C". Inorganica Chimica Acta. 298 (1): 97–102. doi:10.1016/S0020-1693(99)00407-7.
^ abcdeGhosh, Abhik; Berg, Steffen (2014). Arrow Pushing in Inorganic Chemistry: A logical approach to the chemistry of the main-group elements. Hoboken: Wiley. p. 12. ISBN978-1-118-17398-5.
^ abcAppelman, Evan H. (1973-04-01). "Nonexistent compounds. Two case histories". Accounts of Chemical Research. 6 (4). American Chemical Society (ACS): 113–117. doi:10.1021/ar50064a001. ISSN0001-4842.
California State University, Northridge (CSUN). "Standard Reduction Potentials"(PDF). csun.edu. Archived(PDF) from the original on 2017-12-15. Retrieved 2021-11-30.
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