# Standard electrode potential

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Electromotive force of a half reaction cell versus standard hydrogen electrode

Bipolar electrochemistry scheme

In [electrochemistry](/source/Electrochemistry), **standard electrode potential** E ⊖ {\displaystyle E^{\ominus }} , or E r e d ⊖ {\displaystyle E_{red}^{\ominus }} , is the [electrode potential](/source/Electrode_potential) (a measure of the reducing power of any element or compound) which the IUPAC "Gold Book" defines as *"the value of the standard [emf](/source/Electromotive_force) ([electromotive force](/source/Electromotive_force)) of a cell in which molecular hydrogen under [standard pressure](/source/Standard_pressure) is oxidized to solvated protons at the left-hand electrode"*.[1]

## Background

The basis for an [electrochemical cell](/source/Electrochemical_cell), such as the [galvanic cell](/source/Galvanic_cell), is always a [redox reaction](/source/Redox_reaction) which can be broken down into two [half-reactions](/source/Half-reaction): [oxidation](/source/Oxidation) at anode (loss of electron) and [reduction](/source/Redox) at cathode (gain of electron). [Electricity](/source/Electricity) is produced due to the difference of [electric potential](/source/Electric_potential) between the individual potentials of the two metal [electrodes](/source/Electrodes) with respect to the [electrolyte](/source/Electrolyte).

Although the overall potential of a cell can be measured, there is no simple way to accurately measure the [electrode/electrolyte potentials](/source/Absolute_electrode_potential) in isolation. 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.

## Calculation

The [galvanic cell](/source/Galvanic_cell) potential results from the voltage difference of a *pair* of electrodes. It is not possible to measure an absolute value for each electrode separately. However, the potential of a reference electrode, [standard hydrogen electrode](/source/Standard_hydrogen_electrode) (SHE), is defined as to 0.00 V. An electrode with unknown electrode potential can be paired with either the standard hydrogen electrode, or another electrode whose potential has already been measured, to determine its "absolute" potential.

Since the electrode potentials are conventionally defined as reduction potentials, the sign of the potential for the metal electrode being oxidized must be reversed when calculating the overall cell potential. The electrode potentials are independent of the number of electrons transferred —they are expressed in volts, which measure energy per electron transferred—and so the two electrode potentials can be simply combined to give the overall *cell* potential even if different numbers of electrons are involved in the two electrode reactions.

For practical measurements, the electrode in question is connected to the positive terminal of the [electrometer](/source/Electrometer), while the standard hydrogen electrode is connected to the negative terminal.[2]

## Reversible electrode

See also: [Reversible hydrogen electrode](/source/Reversible_hydrogen_electrode)

A reversible electrode is an electrode that owes its potential to [changes of a reversible nature](/source/Reversible_reaction). A first condition to be fulfilled is that the system is close to the [chemical equilibrium](/source/Chemical_equilibrium). A second set of conditions is that the system is submitted to very small solicitations spread on a sufficient period of time so, that the chemical equilibrium conditions nearly always prevail. In theory, it is very difficult to experimentally achieve reversible conditions because any perturbation imposed to a system near equilibrium in a finite time forces it out of equilibrium. However, if the solicitations exerted on the system are sufficiently small and applied slowly, one can consider an electrode to be reversible. By nature, electrode reversibility depends on the experimental conditions and the way the electrode is operated. For example, electrodes used in electroplating are operated with a high over-potential to force the reduction of a given metal cation to be deposited onto a metallic surface to be protected. Such a system is far from equilibrium and continuously submitted to important and constant changes in a short period of time

## Standard reduction potential table

Main article: [Standard electrode potential (data page)](/source/Standard_electrode_potential_(data_page))

See also: [Table of standard reduction potentials for half-reactions important in biochemistry](/source/Table_of_standard_reduction_potentials_for_half-reactions_important_in_biochemistry)

The larger the value of the standard reduction potential, the easier it is for the element to be reduced (gain [electrons](/source/Electron)); in other words, they are better [oxidizing agents](/source/Oxidizing_agent).

For example, F2 has a standard reduction potential of +2.87 V and Li+ has −3.05 V:

- [F 2](/source/Fluorine)(*g*) + 2 *e*−⇌ 2 F− = +2.87 V

- [Li+](/source/Lithium) + *e*−⇌ Li(*s*) = −3.05 V

The highly positive standard reduction potential of F2 means it is reduced easily and is therefore a good oxidizing agent. In contrast, the greatly negative standard reduction potential of Li+ indicates that it is not easily reduced. Instead, Li(*s*) would rather undergo oxidation (hence it is a good [reducing agent](/source/Reducing_agent)).

Zn2+ has a standard reduction potential of −0.76 V and thus can be oxidized by any other electrode whose standard reduction potential is greater than −0.76 V (e.g., H+ (0 V), Cu2+ (0.34 V), F2 (2.87 V)) and can be [reduced](/source/Redox) by any electrode with standard reduction potential less than −0.76 V (e.g. H2 (−2.23 V), Na+ (−2.71 V), Li+ (−3.05 V)).

In a galvanic cell, where a [spontaneous](/source/Spontaneous_process) redox reaction drives the cell to produce an electric potential, [Gibbs free energy](/source/Gibbs_free_energy) Δ G ⊖ {\displaystyle \Delta G^{\ominus }} must be negative, in accordance with the following equation:

- Δ G c e l l ⊖ = − n F E c e l l ⊖ {\displaystyle \Delta G_{cell}^{\ominus }=-nFE_{cell}^{\ominus }} (unit: Joule = Coulomb × Volt)

where n is number of [moles](/source/Mole_(unit)) of electrons per mole of products and F is the [Faraday constant](/source/Faraday_constant), ~ 96 485 C/mol.

As such, the following rules apply:

- If E c e l l ⊖ {\displaystyle E_{cell}^{\ominus }} > 0, then the process is spontaneous ([galvanic cell](/source/Galvanic_cell)): Δ G c e l l ⊖ {\displaystyle \Delta G_{cell}^{\ominus }} < 0, and energy is liberated.

- If E c e l l ⊖ {\displaystyle E_{cell}^{\ominus }} < 0, then the process is non-spontaneous ([electrolytic cell](/source/Electrolytic_cell)): Δ G c e l l ⊖ {\displaystyle \Delta G_{cell}^{\ominus }} > 0, and energy is consumed.

Thus in order to have a spontaneous reaction ( Δ G c e l l ⊖ {\displaystyle \Delta G_{cell}^{\ominus }} < 0), E c e l l ⊖ {\displaystyle E_{cell}^{\ominus }} must be positive, where:

- E c e l l ⊖ = E c a t h o d e ⊖ − E a n o d e ⊖ {\displaystyle E_{cell}^{\ominus }=E_{cathode}^{\ominus }-E_{anode}^{\ominus }}

where E c a t h o d e ⊖ {\displaystyle E_{cathode}^{\ominus }} is the standard potential at the cathode (called as standard cathodic potential or standard reduction potential and E a n o d e ⊖ {\displaystyle E_{anode}^{\ominus }} is the standard potential at the anode (called as standard anodic potential or standard oxidation potential) as given in the [table of standard electrode potential](/source/Standard_electrode_potential_(data_page)).

## See also

- [Nernst equation](/source/Nernst_equation)

- [Pourbaix diagram](/source/Pourbaix_diagram)

- [Solvated electron](/source/Solvated_electron)

- [Standard electrode potential (data page)](/source/Standard_electrode_potential_(data_page))

- [Standard hydrogen electrode](/source/Standard_hydrogen_electrode) (SHE)

- [Biochemically relevant redox potentials (data page)](/source/Table_of_standard_reduction_potentials_for_half-reactions_important_in_biochemistry)

## References

1. **[^](#cite_ref-1)** [IUPAC](/source/International_Union_of_Pure_and_Applied_Chemistry), *[Compendium of Chemical Terminology](/source/IUPAC_books#Gold_Book)*, 5th ed. (the "Gold Book") (2025). Online version: (2006–) "[Standard electrode potential, E⚬](https://goldbook.iupac.org/terms/view/S05912.html)". [doi](/source/Doi_(identifier)):[10.1351/goldbook.S05912](https://doi.org/10.1351%2Fgoldbook.S05912)

1. **[^](#cite_ref-2)** [IUPAC definition of the electrode potential](http://goldbook.iupac.org/E01956.html)

## Further reading

- Zumdahl, Steven S., Zumdahl, Susan A (2000) *Chemistry* (5th ed.), Houghton Mifflin Company. [ISBN](/source/ISBN_(identifier)) [0-395-98583-8](https://en.wikipedia.org/wiki/Special:BookSources/0-395-98583-8)

- Atkins, Peter, Jones, Loretta (2005) *Chemical Principles* (3rd ed.), W.H. Freeman and Company. [ISBN](/source/ISBN_(identifier)) [0-7167-5701-X](https://en.wikipedia.org/wiki/Special:BookSources/0-7167-5701-X)

- Zu, Y, Couture, MM, Kolling, DR, Crofts, AR, Eltis, LD, Fee, JA, Hirst, J (2003) *Biochemistry*, 42, 12400-12408

## External links

- [Standard Electrode Potentials table](http://hyperphysics.phy-astr.gsu.edu/hbase/Tables/electpot.html)

- [Redox Equilibria](https://www.chemguide.co.uk/physical/redoxeqia/introduction.html)

- [Chemistry of Batteries](http://www.science.uwaterloo.ca/~cchieh/cact/c123/battery.html)

- [Electrochemical Cells](http://hyperphysics.phy-astr.gsu.edu/HBASE/Chemical/electrochem.html#c1)

- [STEP in Non-aqueous solvent](http://www.tandfonline.com/doi/abs/10.1080/14786440908564891)

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