Document Type

Article

Publication Date

7-7-2024

Abstract

The reduction of selenate, SeO²₄⁻(aq),in 0.1 M HClO₄ solutions, induced by underpotential deposition, UPD, of Cu on polycrystalline Au electrodes was investigated using the rotating ring-disk electrode, RRDE, technique. Design and implementation of electrode potential-rotation rate protocols made it possible to determine the rates of SeO²₄⁻(aq)reduction as a function of Cu coverage, θCu, as determined by the Bruckenstein method (Swathirajan et al. J. Phys. Chem. 1982, 86, 2480–2485). In agreement with the results reported recently for Au(111) film electrodes (Strobl et al. Electrochimica Acta 2024, 493, 144,298), the reaction was found to proceed only for θCu above a critical value, i.e. ca. 0.39, in this case, and the mechanism is consistent with an initial reversible formation of adsorbed Cu|SeO²₄⁻(ads),followed by its subsequent irreversible reduction, to yield a yet to be identified species denoted as Cu|Se(ads), as the rate determining step. Best fits of the kinetic model yielded values of the equilibrium constant for adduct formation, K, and first order rate constant for adduct reduction, kET, in the range (2.4 – 45) × 10⁶cm³mol⁻¹ and (0.55 – 30) × 10⁻³s⁻¹, respectively, which are close to those found for Au(111). This unique electrocatalytic effect has been attributed to a shift in the potential of zero charge of the bare substrate toward more negative values, induced by the metal UPD, which promotes the adsorption of the oxyanion at potentials more negative than those found for the bare substrate, making it possible to access overpotentials large enough for its further reduction to ensue.

Keywords

electrocatalysis, kinetics, rotating ring disk electrode, selenate reduction, underpotential deposition

Language

English

Publication Title

Electrochimica Acta

Grant

CHE1808592

Rights

© 2024 The Author(s). This is an open access work distributed under the terms of the Creative Commons Attribution-Non-Commercial (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

Creative Commons License

Creative Commons Attribution-NonCommercial 4.0 International License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License

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Chemistry Commons

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