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Sulfur Substitution and Defect Engineering in an Unfavored MnMoO 4 Catalyst for Efficient Hydrogen Evolution under Visible Light
A novel and nonstoichiometric Mn Mo(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...
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Published in: | ACS applied materials & interfaces 2023-05, Vol.15 (18), p.22142-22156 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A novel and nonstoichiometric Mn
Mo(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 Mn
Mo(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. |
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ISSN: | 1944-8244 1944-8252 |
DOI: | 10.1021/acsami.3c02205 |