An electrocatalyst is a catalyst that participates in electrochemical reactions. Electrocatalysts are a specific form of catalysts that function at electrode surfaces or, most commonly, may be the electrode surface itself. An electrocatalyst can be heterogeneous such as a platinized electrode. Homogeneous electrocatalysts, which are soluble, assist in transferring electrons between the electrode and reactants, and/or facilitate an intermediate chemical transformation described by an overall half reaction. Major challenges in electrocatalysts focus on fuel cells. The chloralkali process is a large scale application that uses electrocatalysts. This technology supplies most of the chlorine and sodium hydroxide required by many industries. The cathode is a mixed metal oxide clad titanium anode (also called a dimensionally stable anode). Many organofluorine compounds are produced by electrofluorination. One manifestation of this technology is the Simons process, which can be described as: R3C–H + HF → R3C–F + H2 In the course of a typical synthesis, this reaction occurs once for each C–H bond in the precursor. The cell potential is maintained near 5–6 V. The anode, the electrocatalyst, is nickel-plated. Acrylonitrile is converted to adiponitrile on an industrial scale via electrocatalysis. In general, a catalyst is an agent that increases the speed of a chemical reaction without being consumed by a reaction. Thermodynamically, a catalyst lowers the activation energy required for a chemical reaction to take place. An electrocatalyst is a catalyst that affects the activation energy of an electrochemical reaction. Shown below is the activation energy of chemical reactions as it relates to the energies of products and reactants. The activation energy in electrochemical processes is related to the potential, i.e. voltage, at which a reaction occurs. Thus, electrocatalysts frequently change the potential at which oxidation and reduction processes are observed.

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Related concepts (6)
Faraday efficiency
In electrochemistry, Faraday efficiency (also called faradaic efficiency, faradaic yield, coulombic efficiency or current efficiency) describes the efficiency with which charge (electrons) is transferred in a system facilitating an electrochemical reaction. The word "Faraday" in this term has two interrelated aspects: first, the historic unit for charge is the faraday (F), but has since been replaced by the coulomb (C); and secondly, the related Faraday's constant (F) correlates charge with moles of matter and electrons (amount of substance).
Overpotential
In electrochemistry, overpotential is the potential difference (voltage) between a half-reaction's thermodynamically-determined reduction potential and the potential at which the redox event is experimentally observed. The term is directly related to a cell's voltage efficiency. In an electrolytic cell the existence of overpotential implies that the cell requires more energy than thermodynamically expected to drive a reaction. In a galvanic cell the existence of overpotential means less energy is recovered than thermodynamics predicts.
Metal–organic framework
Metal–organic frameworks (MOFs) are a class of compounds consisting of metal clusters (also known as SBUs) coordinated to organic ligands to form one-, two-, or three-dimensional structures. The organic ligands included are sometimes referred to as "struts" or "linkers", one example being 1,4-benzenedicarboxylic acid (BDC). More formally, a metal–organic framework is an organic-inorganic porous extended structure. An extended structure is a structure whose sub-units occur in a constant ratio and are arranged in a repeating pattern.
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