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Amperometry in chemistry is the detection of ions in a solution based on electric current or changes in electric current. Amperometry is used in electrophysiology to study vesicle release events using a carbon fiber electrode .
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.
Thus, factors that are of critical importance to quantitative amperometry, such as the surface area of the working electrode, completely disappear from amperometric titrations. The chief advantage over other types of titration is the selectivity offered by the electrode potential, as well as by the choice of titrant.
Double-pulsed chronoamperometry waveform showing integrated region for charge determination.. In electrochemistry, chronoamperometry is an analytical technique in which the electric potential of the working electrode is stepped and the resulting current from faradaic processes occurring at the electrode (caused by the potential step) is monitored as a function of time.
Amperometry uses a carbon electrode to record changes in the chemical composition of the oxidized components of a biological solution. Oxidation and reduction is accomplished by changing the voltage at the active surface of the recording electrode in a process known as "scanning".
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Linear potential sweep. In analytical chemistry, linear sweep voltammetry is a method of voltammetry where the current at a working electrode is measured while the potential between the working electrode and a reference electrode is swept linearly in time.