Engineering Sulfur Vacancies in Spinel-Phase Co3S4 for Effective Electrocatalysis of the Oxygen Evolution Reaction

Xiaomin Li; Kaitian Zheng; Jiajun Zhang; Guoning Li; Chunjian Xu

doi:10.1021/acsomega.2c01423

Engineering Sulfur Vacancies in Spinel-Phase Co₃S₄ for Effective Electrocatalysis of the Oxygen Evolution Reaction

ACS Omega. 2022 Mar 31;7(14):12430-12441. doi: 10.1021/acsomega.2c01423. eCollection 2022 Apr 12.

Authors

Xiaomin Li¹, Kaitian Zheng¹, Jiajun Zhang², Guoning Li³, Chunjian Xu¹

Affiliations

¹ School of Chemical Engineering and Technology, State Key Laboratory of Chemical Engineering, Chemical Engineering Research Center, Tianjin University, Tianjin 300072, China.
² Particles and Catalysis Research Group, School of Chemical Engineering, The University of New South Wales, Sydney, NSW 2052, Australia.
³ School of Thermal Engineering, Shandong Jianzhu University, Jinan 250101, China.

Abstract

Restricted by the sluggish kinetics of the oxygen evolution reaction (OER), efficient OER catalysis remains a challenge. Here, a facile strategy was proposed to prepare a hollow dodecahedron constructed by vacancy-rich spinel Co₃S₄ nanoparticles in a self-generated H₂S atmosphere of thiourea. The morphology, composition, and electronic structure, especially the sulfur vacancy, of the cobalt sulfides can be regulated by the dose of thiourea. Benefitting from the H₂S atmosphere, the anion exchange process and vacancy introduction can be accomplished simultaneously. The resulting catalyst exhibits excellent catalytic activity for the OER with a low overpotential of 270 mV to reach a current density of 10 mA cm^-2 and a small Tafel slope of 59 mV dec^-1. Combined with various characterizations and electrochemical tests, the as-proposed defect engineering method could delocalize cobalt neighboring electrons and expose more Co²⁺ sites in spinel Co₃S₄, which lowers the charge transfer resistance and facilitates the formation of Co³⁺ active sites during the preactivation process. This work paves a new way for the rational design of vacancy-enriched transition metal-based catalysts toward an efficient OER.