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The Galvani potential difference is not directly measurable using voltmeters. The measured potential difference between two metal electrodes assembled into a cell does not equal the difference of the Galvani potentials of the two metals (or their combination with the solution Galvani potential) because the cell needs to contain another metal-metal interface, as in the following schematic of a ...
In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction (half-cell or full cell reaction) from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities (often approximated by concentrations) of the chemical species undergoing ...
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 ...
However, the corresponding Gibbs free energy changes (∆G°) must satisfy ∆G° = – z FE°, where z electrons are transferred, and the Faraday constant F is the conversion factor describing Coulombs transferred per mole electrons. Those Gibbs free energy changes can be added.
This forms a galvanic cell, with hydrogen gas forming on the more noble (less active) metal. The resulting electrochemical potential then develops an electric current that electrolytically dissolves the less noble material. A concentration cell can be formed if the same metal is exposed to two different concentrations of electrolyte.
In battery technology, a concentration cell is a limited form of a galvanic cell that has two equivalent half-cells of the same composition differing only in concentrations. One can calculate the potential developed by such a cell using the Nernst equation. [1]
The electrode potential may be either that at equilibrium at the working electrode ("reversible potential"), or a potential with a non-zero net reaction on the working electrode but zero net current ("corrosion potential", "mixed potential"), or a potential with a non-zero net current on the working electrode (like in galvanic corrosion or ...
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 diode. As described above, when describing chemical potential, one has to say "relative to what".