Engineering Sulfur Vacancies in Spinel-Phase Co(3)S(4) for Effective Electrocatalysis of the Oxygen Evolution Reaction

[Image: see text] 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 Co(3)S(4) nanoparticles in a self-generated H(2)S 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 H(2)S 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 Co(2+) sites in spinel Co(3)S(4), which lowers the charge transfer resistance and facilitates the formation of Co(3+) 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.