Distinct solvation patterns of OH− versus H3O+ charge defects at electrified gold/water interfaces govern their properties

Chanbum Park (), Soumya Ghosh, Harald Forbert and Dominik Marx
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Chanbum Park: Ruhr-Universität Bochum
Soumya Ghosh: Ruhr-Universität Bochum
Harald Forbert: Ruhr-Universität Bochum
Dominik Marx: Ruhr-Universität Bochum

Nature Communications, 2025, vol. 16, issue 1, 1-12

Abstract: Abstract Understanding the solvation structures of OH− and H3O+ at metal interfaces is crucial for developing efficient electrochemical devices. In this paper, we present a detailed investigation of the solvation structures of OH− and H3O+ near gold electrodes under alkaline and acidic aqueous conditions, using ab initio molecular dynamics simulations at controlled surface charge density conditions. Our findings reveal that the adsorption tendencies of OH− and H3O+ are strongly influenced by the oscillating net atomic charge of water normal to the electrified interface in concert with the distinct solvation patterns of these charge defects. While OH− preferentially adsorbs onto the gold surface within the first water layer, the positive net atomic charge restricts the closest approach of H3O+ to beyond the first water layer. We unveil resting and active states that support charge transfer processes at the gold/water interface, which critically involve Au atoms in a unique Grotthuss-like mechanism.

Date: 2025
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DOI: 10.1038/s41467-025-63832-1

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