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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.
Latimer diagrams can be used in the construction of Frost diagrams, as a concise summary of the standard electrode potentials relative to the element. Since Δ r G o = -n F E o , the electrode potential is a representation of the Gibbs energy change for the given reduction.
The abstract definition of chemical potential given above—total change in free energy per extra mole of substance—is more specifically called total chemical potential. [13] [14] If two locations have different total chemical potentials for a species, some of it may be due to potentials associated with "external" force fields (electric ...
Diagram of ion concentrations and charge across a semi-permeable cellular membrane. An electrochemical gradient is a gradient of electrochemical potential, usually for an ion that can move across a membrane. The gradient consists of two parts: The chemical gradient, or difference in solute concentration across a membrane.
A concentration cell is an electrochemical cell where the two electrodes are the same material, the electrolytes on the two half-cells involve the same ions, but the electrolyte concentration differs between the two half-cells. An example is an electrochemical cell, where two copper electrodes are submerged in two copper(II) sulfate solutions ...
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 ...
At a real surface the potential is influenced by image charges and the formation of surface dipoles and it rather looks as indicated by the dashed line. Given the potential in Figure 1, it can be shown that the one-dimensional single-electron Schrödinger equation gives two qualitatively different types of solutions. [4]
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 ...