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  2. Table of standard reduction potentials for half-reactions ...

    en.wikipedia.org/wiki/Table_of_standard...

    At pH = 7, when [ H +] = 10 −7 M, the reduction potential of H + differs from zero because it depends on pH. Solving the Nernst equation for the half-reaction of reduction of two protons into hydrogen gas gives: 2 H + + 2 e − ⇌ H 2

  3. Nernst equation - Wikipedia

    en.wikipedia.org/wiki/Nernst_equation

    In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction (half-cell or full cell reaction) from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities (often approximated by concentrations) of the chemical species undergoing ...

  4. Reduction potential - Wikipedia

    en.wikipedia.org/wiki/Reduction_potential

    In aqueous solutions, redox potential is a measure of the tendency of the solution to either gain or lose electrons in a reaction. A solution with a higher (more positive) reduction potential than some other molecule will have a tendency to gain electrons from this molecule (i.e. to be reduced by oxidizing this other molecule) and a solution with a lower (more negative) reduction potential ...

  5. Latimer diagram - Wikipedia

    en.wikipedia.org/wiki/Latimer_diagram

    Latimer diagrams can be used in the construction of Frost diagrams, as a concise summary of the standard electrode potentials relative to the element.Since Δ r G o = -nFE o, the electrode potential is a representation of the Gibbs energy change for the given reduction.

  6. Standard electrode potential (data page) - Wikipedia

    en.wikipedia.org/wiki/Standard_electrode...

    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° = – z FE°,

  7. Jefimenko's equations - Wikipedia

    en.wikipedia.org/wiki/Jefimenko's_equations

    Jefimenko's equations can be found [2] from the retarded potentials φ and A: (,) = (′,) | ′ | ′, (,) = (′,) | ′ | ′, which are the solutions to Maxwell's equations in the potential formulation, then substituting in the definitions of the electromagnetic potentials themselves: =, = and using the relation = replaces the potentials φ and A by the fields E and B.

  8. Exchange current density - Wikipedia

    en.wikipedia.org/wiki/Exchange_current_density

    This ongoing current in both directions is called the exchange current density. When the potential is set more negative than the formal potential, the cathodic current is greater than the anodic current. Written as a reduction, cathodic current is positive. The net current density is the difference between the cathodic and anodic current density.

  9. Pourbaix diagram - Wikipedia

    en.wikipedia.org/wiki/Pourbaix_diagram

    Pourbaix diagram of iron. [1] The Y axis corresponds to voltage potential. In electrochemistry, and more generally in solution chemistry, a Pourbaix diagram, also known as a potential/pH diagram, E H –pH diagram or a pE/pH diagram, is a plot of possible thermodynamically stable phases (i.e., at chemical equilibrium) of an aqueous electrochemical system.