期刊
NEW JOURNAL OF CHEMISTRY
卷 45, 期 31, 页码 14167-14176出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nj00608h
关键词
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资金
- Doctor Foundation of Zhengzhou University of Light Industry [13501050076]
- key project of scientific and technological research of Henan Province [192102310243, 202102310282]
- Program for Science and Technology Innovation Team in Henan Province [CXTD2015023]
Combining different semiconductor materials with diverse geometric structures and energy level configurations can lead to the construction of heterostructured photocatalysts with high activity. The synthesis of a ZnIn2S4-MoS2/TiO2 composite material using a solvothermal method showed outstanding hydrogen production performance, with the optimized weight ratios leading to a significantly improved photocatalytic H-2 evolution rate under simulated sunlight irradiation.
Combining different semiconductor materials with diverse geometric structures and energy level configurations is an effective strategy for constructing heterostructured photocatalysts with high activity. Using a solvothermal method, 1D TiO2 nanobelts were uniformly embedded into the gaps of flower-like 3D ZIS/MoS2 microspheres to allow atomic interactions. Therefore, a 3D ZnIn2S4-MoS2 microsphere/1D TiO2 nanobelt (ZIS/MoS2/TiO2) composite with outstanding hydrogen production performance was synthesized. The unique heterostructure had a favorable energy level distribution and spatial structure, which could improve the interfacial charge transfer. Upon optimizing the weight ratios of the components, the maximum photocatalytic H-2 evolution rate was 8440.28 mu mol g(-1) h(-1) when using the 250%-ZIS/25%-MoS2/TiO2 composite under simulated sunlight irradiation, which was similar to 44.4 and 2181.0 times higher than when using pure ZIS and TiO2, respectively. In addition, apparent quantum efficiency (AQE) values of 39.33% at 380 nm and 30% at 420 nm were achieved. Importantly, the hydrogen production rate was 94.1% of the initial rate after four cycles, showing excellent stability. The photocatalytic hydrogen evolution mechanism of the prepared photocatalyst was also discussed in detail.
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