Search results
Results From The WOW.Com Content Network
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.
The equation for local ion density can be substituted into the Poisson equation under the assumptions that the work being done is only electric work, and that the concentration of salt is much higher than the concentration of ions. [4] The electric work to bring an ion of charge to a surface with potential ψ can be represented by =. [4]
Ionic potential is the ratio of the electrical charge (z) to the radius (r) of an ion. [1]= = As such, this ratio is a measure of the charge density at the surface of the ion; usually the denser the charge, the stronger the bond formed by the ion with ions of opposite charge.
In short, an electric potential is the electric potential energy per unit charge. This value can be calculated in either a static (time-invariant) or a dynamic (time-varying) electric field at a specific time with the unit joules per coulomb (J⋅C −1) or volt (V). The electric potential at infinity is assumed to be zero.
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 electrostatic interaction model of ions in solids has thus been extended to a point multipole concept that also includes higher multipole moments like dipoles, quadrupoles etc. [8] [9] [10] These concepts require the determination of higher order Madelung constants or so-called electrostatic lattice constants.
The electric potential also varies with temperature, concentration and pressure. Since the oxidation potential of a half-reaction is the negative of the reduction potential in a redox reaction, it is sufficient to calculate either one of the potentials. Therefore, standard electrode potential is commonly written as standard reduction potential.
The electrostatic potential energy U E stored in a system of two charges is equal to the electrostatic potential energy of a charge in the electrostatic potential generated by the other. That is to say, if charge q 1 generates an electrostatic potential V 1 , which is a function of position r , then U E = q 2 V 1 ( r 2 ) . {\displaystyle U ...