Fabrication of MoS2@g-C3N4 core-shell nanospheres for visible light photocatalytic degradation of toluene

被引:26
作者
Wang, Xin [1 ]
Xiong, Wei [1 ]
Li, Xinyong [1 ,2 ]
Zhao, Qidong [1 ]
Fan, Shiying [1 ]
Zhang, Mingmei [1 ]
Mu, Jincheng [1 ]
Chen, Aicheng [2 ]
机构
[1] Dalian Univ Technol, Sch Environm Sci & Technol, Key Lab Ind Ecol & Environm Engn MOE, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Univ Guelph, Dept Chem, 50 Stone Rd E, Guelph, ON N1G 2W1, Canada
基金
中国国家自然科学基金;
关键词
MoS2@g-C3N4; Core-shell nanospheres; Visible light photocatalysis; Toluene; Nanostructured catalyst; VOLATILE ORGANIC-COMPOUNDS; HYDROGEN-EVOLUTION CATALYSIS; ONE-STEP SYNTHESIS; GASEOUS TOLUENE; EFFICIENT CATALYST; OXIDATION; TIO2; MOS2; NANOSHEETS; PERFORMANCE;
D O I
10.1007/s11051-018-4340-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The semiconductor-based photocatalytic oxidation process is considered as one of the most economical and environmentally friendly approach for the degradation of toluene. For the sake of exploring an efficient visible-light-driven photocatalysts, the MoS2@g-C3N4 core-shell nanospheres were successfully fabricated by taking the advantages of the morphology and structure of materials tailoring and semiconductor coupling, via a two-step approach including the hydrothermal method followed by ultrasonic adhering approach. The morphology, crystallinity, composition, and optical property of as-prepared catalysts were well characterized. The core-shell structure was fabricated by using MoS2 as the template and the coating of g-C3N4 improved the separation of photoinduced charges, due to the strong electronic interaction between them. The photocatalytic activity of MoS2@g-C3N4 core-shell nanospheres had been investigated by the degradation of toluene under visible light irradiation using in situ Fourier transform infrared (FTIR) spectroscopy. The MoS2@g-C3N4 nanospheres displayed enhanced visible-light photocatalytic activity, which is about 1.3 and 9.6 times than that of g-C3N4 and MoS2 nanospheres under identical conditions. Electron spin resonance (ESR) examinations confirmed the generation of center dot OH and center dot O-2(-), which were the key reactive oxygen species involved in the photocatalytic process.
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页数:12
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