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The auxiliary electrode may be isolated from the working electrode using a glass frit. Such isolation prevents any byproducts generated at the auxiliary electrode from contaminating the main test solution: for example, if a reduction is being performed at the working electrode in aqueous solution, oxygen may be evolved from the auxiliary electrode.
The rate of voltage change over time during each of these phases is known as the scan rate (V/s). In a standard three-electrode cell, the potential is measured between the working electrode and the reference electrode, while the current is measured between the working electrode and the counter electrode.
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 ...
The working electrode is one of the electrodes at which the oxidation/reduction reactions occur—the processes that occur at this electrode are the ones being monitored. The auxiliary electrode (or counter electrode) is the one at which a process opposite from the one taking place at the working electrode occurs.
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.
Electrode potentials of successive elementary half-reactions cannot be directly added. However, the corresponding Gibbs free energy changes (∆G°) must satisfy ∆G° = – z FE°, where z electrons are transferred, and the Faraday constant F is the conversion factor describing Coulombs transferred per mole electrons. Those Gibbs free energy ...
The figure on the left highlights the platinum (Pt) wire electrode which is not a part of the reaction (it’s a catalyst) and can serve as either the anode or cathode. The wire is immersed in an acidic solution with an H2 (g) outlet pumping gaseous hydrogen into the solution. On the surface of the Pt electrode, a half-reaction occurs:
Most electrodes work over a limited range of conditions, such as pH or temperature, outside of this range the electrodes behavior becomes unpredictable. The advantage of a pseudo-reference electrode is that the resulting variation is factored into the system allowing researchers to accurately study systems over a wide range of conditions.