Electrocatalytic Mechanisms for an Oxygen Evolution Reaction at a Rhombohedral Boron Monosulfide Electrode/Alkaline Medium Interface

Satoshi Hagiwara; Fumiaki Kuroda; Takahiro Kondo; Minoru Otani

doi:10.1021/acsami.3c10548

Electrocatalytic Mechanisms for an Oxygen Evolution Reaction at a Rhombohedral Boron Monosulfide Electrode/Alkaline Medium Interface

ACS Appl Mater Interfaces. 2023 Nov 1;15(43):50174-50184. doi: 10.1021/acsami.3c10548. Epub 2023 Oct 19.

Authors

Satoshi Hagiwara¹, Fumiaki Kuroda¹, Takahiro Kondo^{2

3}, Minoru Otani^{1

2}

Affiliations

¹ Center for Computational Sciences, University of Tsukuba, 1-1-1 Ten-nodai, Tsukuba, Ibaraki 305-8577, Japan.
² Department of Materials Science and Tsukuba Research Center for Energy Materials Science, Institute of Pure and Applied Sciences and R&D Center for Zero CO2 Emission with Functional, Tsukuba, Ibaraki 305-8573, Japan.
³ Advanced Institute for Materials Research, Tohoku University, Sendai 980-8577, Japan.

PMID: 37856085
DOI: 10.1021/acsami.3c10548

Abstract

Rhombohedral boron monosulfide (r-BS) with a layer stacking structure is a promising electrocatalyst for an oxygen evolution reaction (OER) within an alkaline solution. We investigated the catalytic mechanisms at the r-BS electrode/alkaline medium interface for an OER using hybrid solvation theory based on the first-principles method combined with classical solution theory. In this study, we elucidate the activities of the OER at the outermost r-BS sheet with and without various surface defects. The Gibbs free energies along the OER path indicate that the boron vacancies at the first and second layers of the r-BS surface (V_B1 and V_B2) can promote the OER. However, we found that the V_B1 is easily occupied by the oxygen atom during the OER, degrading its electrocatalytic performance. In contrast, V_B2 is suitable for the active site of the OER due to its structure stability. Next, we applied a bias voltage with the OER potential to the r-BS electrode. The bias voltage incorporates the positive excess surface charge into pristine r-BS and V_B2, which can be understood by the relationship between the OER potential and potentials of zero charge at the r-BS electrode. Because the OH^- ions are the starting point of the OER, the positively charged surface is kinetically favorable for the electrocatalyst owing to the attractive interaction with the OH^- ions. Finally, we qualitatively discuss the flat-band potential at a semiconductor/alkaline solution interface. It suggests that p-type carrier doping could promote the catalytic performance of r-BS. These results explain the previous measurement of the OER performance with the r-BS-based electrode and provide valuable insights into developing a semiconductor electrode/water interface.

Keywords: classical solution theory; density functional theory; oxygen evolution reaction; rhombohedral boron monosulfide; semiconductor/water interface.