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The reactivity series is sometimes quoted in the strict reverse order of standard electrode potentials, when it is also known as the "electrochemical series". [8] The following list includes the metallic elements of the first six periods. It is mostly based on tables provided by NIST.
Effective concentration (activity) 1 mol/L for each aqueous or amalgamated (mercury-alloyed) species; 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).
The standard hydrogen electrode (SHE), with [ H +] = 1 M works thus at a pH = 0. 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
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.
Charge transfer coefficient, and symmetry factor (symbols α and β, respectively) are two related parameters used in description of the kinetics of electrochemical reactions. They appear in the Butler–Volmer equation and related expressions. The symmetry factor and the charge transfer coefficient are dimensionless. [1]
n is the number of electrons exchanged, like in the Nernst equation, k is the rate constant for the electrode reaction in s −1, F is the Faraday constant, C is the reactive species concentration at the electrode surface in mol/m 2, the plus sign under the exponent refers to an anodic reaction, and a minus sign to a cathodic reaction,
For example, the exchange current densities for platinum and mercury electrodes for reduction of protons differ by a factor of 10 10, indicative of the excellent catalytic properties of platinum. Owing to this difference, mercury is the preferred electrode material at reducing (cathodic) potentials in aqueous solution. [1]
The overall chemical reaction taking place in a cell is made up of two independent half-reactions, which describe chemical changes at the two electrodes. To focus on the reaction at the working electrode, the reference electrode is standardized with constant (buffered or saturated) concentrations of each participant of the redox reaction. [1]
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