Sulfur Substitution and Defect Engineering in an Unfavored MnMoO Catalyst for Efficient Hydrogen Evolution under Visible Light.

A novel and nonstoichiometric MnMo(S,O) oxysulfide catalyst with oxygen vacancies and a partial Mo-to-Mo transition after the substitution of sulfur was synthesized for an efficient photocatalytic hydrogen evolution reaction (PHER). With appropriate sulfur substitution, a MnMoO semiconductor with a wide band gap was converted to MnMo(S,O) with a narrow gap and a suitable band position for PHER. MnMo oxysulfide of 50 mg achieved a high PHER rate of 415.8 μmol/h under visible light, an apparent quantum efficiency (AQE) of 4.31% at 420 nm, and a solar-to-hydrogen (STH) conversion efficiency of 1.28%. Oxygen vacancies (V) surrounded by low coordination metal atoms act as active reaction sites, which strengthen water adsorption and activation. Here, we demonstrate that sulfur substitution of MnMoO for lowering its wide band gap can not only disturb the strict periodicity of the lattice but also the valence states of Mn and Mo for enhancing PHER via material design.