摘要
In light of the energy and environmental crises humanity faces, photocatalytic hydrogen production has emerged as one of the effective solutions. Nevertheless, the development of high-performance, low-energy-consumption, and long-lasting stable photocatalysts remains extremely urgent. In this study, a NiS-Mn 2 SnS 4 /g-C 3 N 4 composite with efficient photocatalytic hydrogen evolution performance is synthesized via a simple physical mixing method and calcination process. The introduction of NiS and Mn 2 SnS 4 significantly increases the specific surface area of the g-C 3 N 4 composite, and a dual Type-II heterojunction capable of efficiently separating electron-hole pairs is formed between the components and g-C 3 N 4 . Under 300 W xenon lamp irradiation, the NiS-Mn 2 SnS 4 /g-C 3 N 4 composite achieves a hydrogen evolution rate of 7672.45 μmol·g −1 ·h −1 , corresponding to 3.76, 59.74, and 254.64 times enhancements compared to bare g-C 3 N 4 , NiS, and Mn 2 SnS 4 , respectively. After four cycles, the hydrogen production of NiS-Mn 2 SnS 4 /g-C 3 N 4 still reaches 91 % of the rate in the first cycle. Photoelectrochemical property characterization demonstrates that the composite samples can generate more active sites, reduce the overpotential for H 2 evolution, and enhance light absorption efficiency. Combined with density functional theory (DFT) calculations and band structure analysis, it is confirmed that a strong electronic coupling effect exists among NiS, Mn 2 SnS 4 , and g-C 3 N 4 , and the electron transfer follows a Type-II pathway. This study provides important references and insights for constructing high-activity and high-specific-surface-area g-C 3 N 4 -based photocatalysts.
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