Sisyphus effects in hydrogen electrochemistry on metal silicides enabled by silicene subunit edge

Zechao Zhuang; Yong Li; Jiazhao Huang; Zilan Li; Kangning Zhao; Yunlong Zhao; Lin Xu; Liang Zhou; Lyudmila V Moskaleva; Liqiang Mai

doi:10.1016/j.scib.2019.04.005

Sisyphus effects in hydrogen electrochemistry on metal silicides enabled by silicene subunit edge

Sci Bull (Beijing). 2019 May 15;64(9):617-624. doi: 10.1016/j.scib.2019.04.005. Epub 2019 Apr 2.

Authors

Affiliations

¹ State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070, China.
² Institute of Applied and Physical Chemistry and Center for Environmental Research and Sustainable Technology, University of Bremen, Bremen 28359, Germany.
³ Advanced Technology Institute, University of Surrey, Guildford, Surrey GU2 7XH, UK.
⁴ Institute of Applied and Physical Chemistry and Center for Environmental Research and Sustainable Technology, University of Bremen, Bremen 28359, Germany; Department of Chemistry, University of the Free State, Bloemfontein 9300, South Africa. Electronic address: moskaleva@uni-bremen.de.
⁵ State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070, China. Electronic address: mlq518@whut.edu.cn.

PMID: 36659630
DOI: 10.1016/j.scib.2019.04.005

Abstract

Nonmetal elements strictly govern the electrochemical performance of molybdenum compounds. Yet, the exact role played by nonmetals during electrocatalysis remains largely obscure. With intermetallic MoSi₂ comprising silicene subunits, we present an unprecedented hydrogen evolution reaction (HER) behavior in aqueous alkaline solution. Under continuous operation, the HER activity of MoSi₂ shows a more than one order of magnitude improvement in current density from 1.1 to 21.5 mA cm^-2 at 0.4 V overpotential. Meanwhile, this activation behavior is highly reversible, such that voltage withdrawal leads to catalyst inactivation but another operation causes reactivation. Thus, the system shows dynamics strikingly analogous to the legendary Sisyphus' labor, which drops and recovers in a stepwise manner repeatedly, but never succeeds in reaching the top of the mountain. Isomorphic WSi₂ behaves almost the same as MoSi₂, whereas other metal silicides with silicyne subunits, including CrSi₂ and TaSi₂, do not exhibit any anomalous behavior. A thin amorphous shell of MoSi₂ is observed after reaction, within which the Si remains partially oxidized while the oxidation state of Mo is basically unchanged. First-principles calculations further reveal that the adsorption of hydroxide ions on silicene subunit edges and the subsequent Si vacancy formation in MoSi₂ jointly lead to the anomalous HER kinetics of the adjacent Mo active centers. This work demonstrates that the role of nonmetal varies dramatically with the electronic and crystallographic structures of silicides and that silicene structural subunit may serve as a promoter for boosting HER in alkaline media.

Keywords: Electrochemistry; Hydrogen evolution reaction; Metal silicides; Silicene subunit; Sisyphus effect.