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Potential as a function of time for anodic stripping voltammetry Three-electrode setup: (1) working electrode; (2) counter electrode; (3) reference electrode. Voltammetry experiments investigate the half-cell reactivity of an analyte. Voltammetry is the study of current as a function of applied potential. These curves I = f(E) are called ...
Chronoamperometry is typically carried out in unstirred solution and at the fixed electrode, i.e., under experimental conditions avoiding convection as the mass transfer to the electrode. On the other hand, voltammetry is a subclass of amperometry, in which the current is measured by varying the potential applied to the electrode.
Cathodic stripping voltammetry is a voltammetric method for quantitative determination of specific ionic species. [6] It is similar to the trace analysis method anodic stripping voltammetry, except that for the plating step, the potential is held at an oxidizing potential, and the oxidized species are stripped from the electrode by sweeping the potential negatively.
By contrast, in normal pulse voltammetry the current resulting from a series of ever larger potential pulses is compared with the current at a constant 'baseline' voltage. Another type of pulse voltammetry is squarewave voltammetry , which can be considered a special type of differential pulse voltammetry in which equal time is spent at the ...
In electrochemistry, cyclic voltammetry (CV) is a type of voltammetric measurement where the potential of the working electrode is ramped linearly versus time. Unlike in linear sweep voltammetry , after the set potential is reached in a CV experiment, the working electrode 's potential is ramped in the opposite direction to return to the ...
In electrochemistry, the auxiliary electrode, often also called the counter electrode, is an electrode used in a three-electrode electrochemical cell for voltammetric analysis or other reactions in which an electric current is expected to flow.
In analytical chemistry, hydrodynamic voltammetry is a form of voltammetry in which the analyte solution flows relative to a working electrode. [ 1 ] [ 2 ] In many voltammetry techniques, the solution is intentionally left still to allow diffusion -controlled mass transfer .
Fast-scan cyclic voltammetry (FSCV) is cyclic voltammetry with a very high scan rate (up to 1 × 10 6 V·s −1). [1] Application of high scan rate allows rapid acquisition of a voltammogram within several milliseconds and ensures high temporal resolution of this electroanalytical technique. An acquisition rate of 10 Hz is routinely employed.