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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.
Photoelectrochemistry is a subfield of study within physical chemistry concerned with the interaction of light with electrochemical systems. [ 1 ] [ 2 ] It is an active domain of investigation. One of the pioneers of this field of electrochemistry was the German electrochemist Heinz Gerischer .
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 ...
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.
In electrochemistry, the electrochemical potential of electrons (or any other species) is the total potential, including both the (internal, nonelectrical) chemical potential and the electric potential, and is by definition constant across a device in equilibrium, whereas the chemical potential of electrons is equal to the electrochemical ...
The upper graph shows the current density as function of the overpotential η . The anodic and cathodic current densities are shown as j a and j c, respectively for α=α a =α c =0.5 and j 0 =1mAcm −2 (close to values for platinum and palladium). The lower graph shows the logarithmic plot for different values of α (Tafel plot).
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 ...
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.