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English chemist John Daniell (left) and physicist Michael Faraday (right), both credited as founders of electrochemistry.. Electrochemistry is the branch of physical chemistry concerned with the relationship between electrical potential difference and identifiable chemical change.
Potentiometry passively measures the potential of a solution between two electrodes, affecting the solution very little in the process. One electrode is called the reference electrode and has a constant potential, while the other one is an indicator electrode whose potential changes with the sample's composition.
The electrochemical mechanisms of electrocatalytic processes are a common research subject for various fields of chemistry and associated sciences. This is important to the development of water oxidation and fuel cells catalysts. For example, half the water oxidation reaction is the reduction of protons to hydrogen, the subsequent half reaction.
A well-known electrosynthesis is the Kolbe electrolysis, in which two carboxylic acids decarboxylate, and the remaining structures bond together:; A variation is called the non-Kolbe reaction when a heteroatom (nitrogen or oxygen) is present at the α-position.
Electrochemical kinetics is the field of electrochemistry that studies the rate of electrochemical processes. This includes the study of how process conditions, such as concentration and electric potential, influence the rate of oxidation and reduction reactions that occur at the surface of an electrode, as well as an investigation into electrochemical reaction mechanisms.
The beginnings of bioelectrochemistry, as well as those of electrochemistry, are closely related to physiology through the works of Luigi Galvani and then Alessandro Volta. The first modern work in this field is considered that of the German physiologist Julius Bernstein (1902) concerning the source of biopotentials due to different ion ...
[3] Galvanic cell with no cation flow. A wire connects two different metals (e.g. zinc and copper). Each metal is in a separate solution; often the aqueous sulphate or nitrate forms of the metal, however more generally metal salts and water which conduct current. [4]
In such cases, the electron transfer is termed intermolecular electron transfer. A famous example of an inner sphere ET process that proceeds via a transitory bridged intermediate is the reduction of [CoCl(NH 3) 5] 2+ by [Cr(H 2 O) 6] 2+. [5] [6] In this case, the chloride ligand is the bridging ligand that covalently connects the redox ...