Tag Archives: voltammetry

Multicomponent Analysis in Voltammetry

Voltammetry is a particularly attractive technique for the analysis of samples containing two or more analytes. Provided that the analytes behave independently, the voltammogram of a multicomponent mixture is a summation of each analyte’s individual voltammograms. As shown here, if … Continue reading

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Effect of Scan Rate in Cyclic Voltammetry

In a cyclic voltammetry experiment, scanning the potential in both directions provides with the opportunity to explore the electrochemical behavior of species generated at the electrode. This is a distinct advantage of cyclic voltammetry over other voltammetric techniques. The illustration … Continue reading

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Cyclic Voltammetry

In cyclic voltammetry (CV) we scan the potential in both the cathodic and anodic directions. The illustration below shows a typical potential-excitation signal (a) in which we first scan the potential to more positive values, oxidizing R to O, and … Continue reading

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Anodic Stripping Voltammetry

As illustrated here, anodic stripping voltammetry (ASV) consists of two steps. The first step is a controlled potential electrolysis in which we hold the working electrode—usually a hanging mercury drop or a mercury film electrode—at a cathodic potential sufficient to … Continue reading

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Pulse Polarography

Normal polarography has been replaced by various forms of pulse polarography, several examples of which are shown here. Normal pulse polarography (a), for example, uses a series of potential pulses characterized by a cycle of time of τ, a pulse-time … Continue reading

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Normal Polarography

The first important voltammetric technique to be developed—polarography—uses the dropping mercury electrode as the working electrode. As shown here, the current flowing through the electrochemical cell is measured while applying a linear potential ramp. Although polarography takes place in an … Continue reading

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Shape of Voltammograms

In voltammetry we measure current as a function of the applied potential. The shape of a voltammogram is determined by several experimental factors, the most important of which are how we measure the current and whether convection is included as … Continue reading

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Origin of Faradaic Current in Voltammetry

Let’s assume we have a solution that is 1.0 mM in Fe(CN)63– is 1.0 mM. The standard state potential for the reduction of Fe(CN)63– to Fe(CN)64– is +0.356 V. If we apply a potential of +0.550 V the concentration of Fe(CN)63– at the electrode’s surface … Continue reading

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Electrochemical Cell for Voltammetry

A typical arrangement for a voltammetric electrochemical cell is shown here. In addition to the working electrode, the reference electrode, and the auxiliary electrode, the cell also includes a N2-purge line for removing dissolved O2, and an optional stir bar. … Continue reading

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Family Tree for Interfacial Electrochemical Techniques

Shown here is a family tree that highlights a number of interfacial electrochemical techniques. The specific techniques are shown in red, the experimental conditions are shown in blue, and the analytical signals are shown in green. At the first level, … Continue reading

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