Search results
Results from the WOW.Com Content Network
Tafel plot for an anodic process (). The Tafel equation is an equation in electrochemical kinetics relating the rate of an electrochemical reaction to the overpotential. [1] The Tafel equation was first deduced experimentally and was later shown to have a theoretical justification.
Randles circuit schematic. In electrochemistry, a Randles circuit is an equivalent electrical circuit that consists of an active electrolyte resistance R S in series with the parallel combination of the double-layer capacitance C dl and an impedance (Z w) of a faradaic reaction.
Charge transfer coefficient, and symmetry factor (symbols α and β, respectively) are two related parameters used in description of the kinetics of electrochemical reactions. They appear in the Butler–Volmer equation and related expressions. The symmetry factor and the charge transfer coefficient are dimensionless. [1]
Pourbaix diagram of iron. [1] The Y axis corresponds to voltage potential. In electrochemistry, and more generally in solution chemistry, a Pourbaix diagram, also known as a potential/pH diagram, E H –pH diagram or a pE/pH diagram, is a plot of possible thermodynamically stable phases (i.e., at chemical equilibrium) of an aqueous electrochemical system.
The exchange current can be thought of as a background current to which the net current observed at various overpotentials is normalized. For a redox reaction written as a reduction at the equilibrium potential, electron transfer processes continue at electrode/solution interface in both directions.
The Koutecký–Levich equation models the measured electric current at an electrode from an electrochemical reaction in relation to the kinetic activity and the mass transport of reactants. A visualization of the Koutecký–Levich equation. The graph shows the measured current as a function of the mass transport current for given kinetic current.
The basic setup in electrosynthesis is a galvanic cell, a potentiostat and two electrodes. Typical solvent and electrolyte combinations minimizes electrical resistance . [ 5 ] Protic conditions often use alcohol-water or dioxane -water solvent mixtures with an electrolyte such as a soluble salt , acid or base .
To focus on the reaction at the working electrode, the reference electrode is standardized with constant (buffered or saturated) concentrations of each participant of the redox reaction. [1] There are many ways reference electrodes are used. The simplest is when the reference electrode is used as a half-cell to build an electrochemical cell.