期刊
DALTON TRANSACTIONS
卷 47, 期 16, 页码 5652-5659出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8dt00356d
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资金
- Zhejiang Provincial Natural Science Foundation of China [LQ16B030002]
- National Natural Science Foundation of China [61504063, 51572065, 51502068, 51772071, 61504034]
- Natural Science Foundation of Jiangsu Higher Education Institutions of China [15KJB430023]
- Zhejiang Provincial Natural Science Foundation for Distinguished Young Scholars [LR15E020001]
Expanding the photoresponse range of TiO2-based photocatalysts is of great interest for photocatalytic H-2 production. Herein, noble-metal-free CuInS2 quantum dots were employed as a novel inorganic dye to expand the visible light absorption of TiO2/MoS2 for solar H-2 generation. The as(-)prepared CuInSz/TiO2/MoS2 photocatalysts exhibit broad absorption from the ultraviolet to near-infrared region. Under visible light irradiation (lambda > 420 nm), the CuInS2/TiO2/MoS2 photocatalyst with 0.6 mmol(-1) CuInS2 and 0.5 wt% MoS2 showed the highest H-2 evolution rate with a value of 1034 mu mol h(-1) g(-1). Moreover, a considerable H-2 evolution rate of 141 mu mol h(-1) g(-1) was obtained under the irradiation of the optimized CuInS2/TiO2/MoS2 photocatalyst with >500 nm light. The reaction mechanism of the CuInS2/TiO2/MoS2 photocatalyst for photocatalytic H-2 evolution was investigated in detail by photoluminescence decay study, and the results showed that the photoexcited electrons of CuInS2 can be transferred efficiently through TiO2 to MoS2 and then react with the absorbed protons to generate H-2 The reported sensitization strategy tremendously improves the visible light absorption capacity and the photocatalytic performance of TiO2-based photocatalysts.
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