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Differential pulse voltammetry (DPV) (also differential pulse polarography, DPP) is a voltammetry method used to make electrochemical measurements and a derivative of linear sweep voltammetry or staircase voltammetry, with a series of regular voltage pulses superimposed on the potential linear sweep or stairsteps.
Differential pulse voltammetry: An electrochemical technique similar to normal pulse voltammetry but the applied base potential is increased or decreased steadily, and the pulse height: base height ratio is kept constant. In DPV, measurements of current are taken twice during each drop, first immediately before the pulse and second before the ...
Cell of cyclic voltammetry. Double potential step chronoamperometry (DPSCA) is the technique whose working electrode is applied by the potential stepping forward for a certain period of time and backward for a period of time. The current is monitored and plotted with respect to time. This method starts with an induction period.
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.
Polarography is a type of voltammetry where the working electrode is a dropping mercury electrode (DME) or a static mercury drop electrode (SMDE), which are useful for their wide cathodic ranges and renewable surfaces. It was invented in 1922 by Czechoslovak chemist Jaroslav Heyrovský, for which he won the Nobel prize in 1959.
where Δi p is the differential current peak value, A is the surface area of the electrode, C 0 * is the concentration of the species, D 0 is the diffusivity of the species, t p is the pulse width, and ΔΨ p is a dimensionless parameter which gauges the peak height in SWV relative to the limiting response in normal pulse voltammetry. [4]
Examples of pulse shapes: (a) rectangular pulse, (b) cosine squared (raised cosine) pulse, (c) Dirac pulse, (d) sinc pulse, (e) Gaussian pulse. A pulse in signal processing is a rapid, transient change in the amplitude of a signal from a baseline value to a higher or lower value, followed by a rapid return to the baseline value. [1]
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 .