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The phrase "chemical potential" sometimes means "total chemical potential", but that is not universal. [13] In some fields, in particular electrochemistry, semiconductor physics, and solid-state physics, the term "chemical potential" means internal chemical potential, while the term electrochemical potential is used to mean total chemical ...
These two examples show that an electrical potential and a chemical potential can both give the same result: A redistribution of the chemical species. Therefore, it makes sense to combine them into a single "potential", the electrochemical potential , which can directly give the net redistribution taking both into account.
When a voltmeter is used to measure an electronic device, it does not quite measure the pure electric potential (also called Galvani potential).Instead, it measures the electrochemical potential, also called "fermi level difference", which is the total free energy difference per electron, including not only its electric potential energy but also all other forces and influences on the electron ...
Under the free electron model, the electrons in a metal can be considered to form a Fermi gas. The number density N / V {\displaystyle N/V} of conduction electrons in metals ranges between approximately 10 28 and 10 29 electrons/m 3 , which is also the typical density of atoms in ordinary solid matter.
The chemical potential μ is, by definition, the energy of adding an extra electron to the fluid. This energy may be decomposed into a kinetic energy T part and the potential energy − eφ part. Since the chemical potential is kept constant, Δ μ = Δ T − e Δ ϕ = 0. {\displaystyle \Delta \mu =\Delta T-e\Delta \phi =0.}
A list of the electron affinities was used by Robert S. Mulliken to develop an electronegativity scale for atoms, equal to the average of the electrons affinity and ionization potential. [2] [3] Other theoretical concepts that use electron affinity include electronic chemical potential and chemical hardness.
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 ...
An example is the London-Eyring-Polanyi-Sato potential [2] [3] [4] for the system H + H 2 as a function of the three H-H distances. For more complicated systems, calculation of the energy of a particular arrangement of atoms is often too computationally expensive for large scale representations of the surface to be feasible.