4.6 Article

A simulation and experimental study of electrochemical pH control at gold interdigitated electrode arrays

Journal

ELECTROCHIMICA ACTA
Volume 395, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2021.139113

Keywords

Finite element analysis simulation; Tailored in-situ pH control; Solid state sensors; Electroanalysis; Microband interdigitated electrode array

Funding

  1. Irish Research Council [GOIPG/2015/2925]
  2. VistaMilk Centre Sci-ence Foundation Ireland (SFI)
  3. Department of Agriculture, Food and the Marine (DAFM) [16/RC/3835]

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In electroanalysis, solution pH is critical for detecting specific analytes and can be controlled by chemicals or electrochemical in-situ methods. Finite element analysis guides experimental design on interdigitated electrodes for pH control. The applied current and electrode spacing directly impact proton generation and pH change.
In electroanalysis, solution pH is a critical parameter that often needs to be tailored and controlled for the detection of particular analytes. This is most commonly performed by the addition of chemicals, such as strong acids or bases. Electrochemical in-situ pH control offers the possibility for the local adjustment of pH at the point of detection, without the need for additional reagents. Finite element analysis (FEA) simulations have been performed on interdigitated electrodes, to guide experimental design in relation to both electroanalysis and in-situ control of solution pH. No previous model exists that describes the gen-eration of protons at an interdigitated electrode arrays in solution with one comb acting as a protonator, and the other as the sensor. In this work, FEA models are developed to provide insight into the optimum conditions necessary for electrochemical pH control. The magnitude of applied galvanostatic current has a direct relation to the flux of protons generated and subsequent change in pH. Increasing the separa-tion between the electrodes increases the time taken for protons to diffuse across the gap between the electrode combs. The final pH achieved after 1 second, at both protonator and sensor electrodes, was shown to be largely uninfluenced by a solution's initial pH. The impact of buffer concentration was also modelled and investigated. In practice, the pH at the electrode surface was probed by means of cyclic voltammetry, i.e., to identify the potential of the gold oxide reduction peak. A pH indicator, methyl red, was used to visualise the solution pH change at the electrodes, comparing well with the model's pre-diction. Finally, we show that in-situ pH controlled detection of mercury in water, using square wave stripping voltammetry, is almost identical to samples acidified to pH 3.5 using nitric acid. (c) 2021 Elsevier Ltd. All rights reserved.

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