Copper vacancy activated plasmonic Cu3−xSnS4 for highly efficient photocatalytic hydrogen generation: Broad solar absorption, efficient charge separation and decreased HER overpotential

Broad absorption spectra with efficient generation and separation of available charge carriers are indispensable requirements for promising semiconductor-based photocatalysts to achieve the ultimate goal of solar-to-fuel conversion. Here, Cu 3− x SnS 4 ( x = 0−0.8) with copper vacancies have been prepared and fabricated via solvothermal process. The obtained copper vacancy materials have extended light absorption from ultraviolet to near-infrared-II region for its significant plasmonic effects. Time-resolved photoluminescence shows that the vacancies can simultaneously optimize charge carrier dynamics to boost the generation of long-lived active electrons for photocatalytic reduction. Density functional theory calculations and electrochemical characterizations further revealed that copper vacancies in Cu 3− x SnS 4 tend to enhance hydrogen’s adsorption energy with an obvious decrease in its H 2 evolution reaction (HER) overpotential. Furthermore, without any loadings, the H 2 production rate was measured to be 9.5 mmol·h −1 ·g −1 . The apparent quantum yield was measured to be 27% for wavelength λ > 380 nm. The solar energy conversion efficiency was measured to be 6.5% under visible-near infrared (vis-NIR) ( λ > 420 nm).