Overview
FrançaisABSTRACT
This article deals with the various existing means in order to improve the performances of voltammetric techniques on solid electrode in chemical analysis. Two parameters are particularly concerned by this improvement research: selectivity and the lowering of the detection limit. The derived voltammetry allows for optimizing selectivity. Concerning the lowering of the detection limit, which could allow for reaching the domain of traces, the lowering of the residual current by means of the pulse voltammetry or the amplifying of the faradic current by means of the redissolution voltammetry appear to provide interesting solutions.
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Read the articleAUTHORS
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Fethi BEDIOUI: Engineer ENSCP (École nationale supérieure de chimie de Paris) - Doctor of Science - Research Director, CNRS
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Sophie GRIVEAU: Doctorate from Pierre et Marie Curie University - Senior lecturer at ENSCP (École Nationale Supérieure de Chimie de Paris)
INTRODUCTION
In this third section, we look at the various ways in which the performance of voltammetric techniques on solid electrodes can be improved with a view to their application in chemical analysis. Improvements in selectivity and lowering the detection limit (to reach the trace analysis range) are the main areas of focus. With regard to selectivity, voltammetric techniques can be improved by deriving voltammograms. This latter approach has given rise to derivative voltammetry, which has enjoyed considerable success in polarography. As far as improving the detection limit is concerned, it has been shown that, in most cases, this can be achieved either by minimizing the residual current by filtering the capacitive current, or by amplifying the faradic current as a result of the accumulation of electroactive substance near the surface of the indicator electrode. These approaches gave rise to pulse voltammetry and redissolution voltammetry respectively.
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Voltammetry on solid electrode
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