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  2. Standard electrode potential (data page) - Wikipedia

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

    Electrode potentials of successive elementary half-reactions cannot be directly added. However, the corresponding Gibbs free energy changes (∆G°) must satisfy ∆G° = – z FE°, where z electrons are transferred, and the Faraday constant F is the conversion factor describing Coulombs transferred per mole electrons. Those Gibbs free energy ...

  3. Standard electrode potential - Wikipedia

    en.wikipedia.org/wiki/Standard_electrode_potential

    Bipolar electrochemistry scheme. In electrochemistry, standard electrode potential, or , is a measure of the reducing power of any element or compound.The IUPAC "Gold Book" defines it as; "the value of the standard emf (electromotive force) of a cell in which molecular hydrogen under standard pressure is oxidized to solvated protons at the left-hand electrode".

  4. Electrode potential - Wikipedia

    en.wikipedia.org/wiki/Electrode_potential

    To avoid possible ambiguities, the electrode potential thus defined can also be referred to as Gibbs–Stockholm electrode potential. In both conventions, the standard hydrogen electrode is defined to have a potential of 0 V. Both conventions also agree on the sign of E for a half-cell reaction when it is written as a reduction.

  5. Electroanalytical methods - Wikipedia

    en.wikipedia.org/wiki/Electroanalytical_methods

    Chronoamperometry is typically carried out in unstirred solution and at the fixed electrode, i.e., under experimental conditions avoiding convection as the mass transfer to the electrode. On the other hand, voltammetry is a subclass of amperometry, in which the current is measured by varying the potential applied to the electrode.

  6. Cyclic voltammetry - Wikipedia

    en.wikipedia.org/wiki/Cyclic_voltammetry

    The solvent, electrolyte, and material composition of the working electrode will determine the potential range that can be accessed during the experiment. The electrodes are immobile and sit in unstirred solutions during cyclic voltammetry. This "still" solution method gives rise to cyclic voltammetry's characteristic diffusion-controlled peaks.

  7. 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 ...

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

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

    When working at the frontier between inorganic and biological processes (e.g., when comparing abiotic and biotic processes in geochemistry when microbial activity could also be at work in the system), care must be taken not to inadvertently directly mix standard reduction potentials (versus SHE, pH = 0) with formal (or apparent) reduction ...

  9. Reference electrode - Wikipedia

    en.wikipedia.org/wiki/Reference_electrode

    Most electrodes work over a limited range of conditions, such as pH or temperature, outside of this range the electrodes behavior becomes unpredictable. The advantage of a pseudo-reference electrode is that the resulting variation is factored into the system allowing researchers to accurately study systems over a wide range of conditions.