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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 ...
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. Therefore, the difference in ...
For example, n-type silicon has a higher internal chemical potential of electrons than p-type silicon. In a p–n junction diode at equilibrium the chemical potential (internal chemical potential) varies from the p-type to the n-type side, while the total chemical potential (electrochemical potential, or, Fermi level) is constant throughout the ...
For example, the absolute half-cell entropy has been defined as the entropy of the absolute half-cell process defined above. [4] An alternative definition of the absolute half-cell entropy has recently been published by Fang et al. [5] who define it as the entropy of the following reaction (using the hydrogen electrode as an example):
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.
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.
To avoid possible ambiguities, the electrode potential thus defined can also be referred to as Gibbs–Stockholm electrode potential. In both conventions, the standard hydrogen electrode is defined to have a potential of 0 V. Both conventions also agree on the sign of E for a half-cell reaction when it is written as a reduction.
The electric potential and the magnetic vector potential together form a four-vector, so that the two kinds of potential are mixed under Lorentz transformations. Practically, the electric potential is a continuous function in all space, because a spatial derivative of a discontinuous electric potential yields an electric field of impossibly ...