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  2. 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".

  3. Standard electrode potential (data page) - Wikipedia

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

    For example, from Fe 2+ + 2 e − ⇌ Fe(s) (–0.44 V), the energy to form one neutral atom of Fe(s) from one Fe 2+ 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 (∆ G f °) for an Fe 2+ ion, since e − and Fe( s ) both have zero formation energy.

  4. Randles–Sevcik equation - Wikipedia

    en.wikipedia.org/wiki/Randles–Sevcik_equation

    In electrochemistry, the Randles–Ševčík equation describes the effect of scan rate on the peak current (i p) for a cyclic voltammetry experiment. For simple redox events where the reaction is electrochemically reversible, and the products and reactants are both soluble, such as the ferrocene/ferrocenium couple, i p depends not only on the concentration and diffusional properties of the ...

  5. Galvanic cell - Wikipedia

    en.wikipedia.org/wiki/Galvanic_cell

    In the strictest sense, a battery is a set of two or more galvanic cells that are connected in series to form a single source of voltage. For instance, a typical 12 V lead–acid battery has six galvanic cells connected in series, with the anodes composed of lead and cathodes composed of lead dioxide, both immersed in sulfuric acid .

  6. Iron redox flow battery - Wikipedia

    en.wikipedia.org/wiki/Iron_redox_flow_battery

    During charge, hydrogen will evolve, as the standard potential of the hydrogen evolution reaction (HER) lies between the standard potential of Fe 2+ /Fe 3+ and of Fe 2+ /Fe 0. The acidic protons H + in solution react to form hydrogen gas (Reaction 7) whilst iron(II) oxidises in the positive half-cell (Reaction 6). The HER is pH dependent.

  7. Iron oxide cycle - Wikipedia

    en.wikipedia.org/wiki/Iron_oxide_cycle

    It is based on the reduction and subsequent oxidation of iron ions, particularly the reduction and oxidation between Fe 3+ and Fe 2+. The ferrites, or iron oxide, begins in the form of a spinel and depending on the reaction conditions, dopant metals and support material forms either Wüstites or different spinels.

  8. Iron(II) hydroxide - Wikipedia

    en.wikipedia.org/wiki/Iron(II)_hydroxide

    3 Fe(OH) 2 → Fe 3 O 4 + H 2 + 2 H 2 O. Anions such as selenite and selenate can be easily adsorbed on the positively charged surface of iron(II) hydroxide, where they are subsequently reduced by Fe 2+. The resulting products are poorly soluble (Se 0, FeSe, or FeSe 2).

  9. Ion transport number - Wikipedia

    en.wikipedia.org/wiki/Ion_transport_number

    The exact relationship depends on the nature of the reactions at the two electrodes. For the electrolysis of aqueous copper(II) sulfate (CuSO 4) as an example, with Cu 2+ (aq) and SO 2− 4 (aq) ions, the cathode reaction is the reduction Cu 2+ (aq) + 2 e − → Cu(s) and the anode reaction is the corresponding oxidation of Cu to Cu 2+.