Assemble of Bi-doped TiO2 onto 2D MoS2: an efficient p-n heterojunction for photocatalytic H2 generation under visible light

被引:21
|
作者
Bera, Susmita [1 ]
Kumari, Ankita [1 ,2 ]
Ghosh, Srabanti [1 ]
Basu, Rajendra N. [1 ]
机构
[1] CSIR Cent Glass & Ceram Res Inst, Energy Mat & Devices Div, 196 Raja SC Mullick Rd, Kolkata 700032, India
[2] Indian Inst Technol Kharagpur, Sch Energy Sci Engn, Kharagpur, W Bengal, India
关键词
Bi-doped TiO2; p– n heterojunction; photocatalytic activity; water splitting; interfacial charge transfer;
D O I
10.1088/1361-6528/abe152
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Fabrication of noble-metal-free, efficient and stable hybrid photocatalyst is essential to address the rapidly growing energy crisis and environmental pollution. Here, MoS2 has been used as the co-catalyst on Bi-doped TiO2 to form a novel heterostructure to increase the utilization of the photogenerated charge carriers for improving photocatalytic H-2 evolution activity through water reduction. Significantly increased photocatalytic H-2 generation has been achieved on the optimized MoS2/Bi-TiO2 nanocomposite (similar to 512 mu mol g(-1)) after 4 h of visible light illumination, which is nine times higher than that of the pristine TiO2 (similar to 57 mu mol g(-1)). The measurements of photocurrent, charge transfer resistance and photo-stability of MoS2/Bi-TiO2 photoanode imply that charge separation efficiency has been improved in comparison to the pure MoS2 and TiO2 photoanodes. Further, the Mott-Schottky study confirmed that a p-n heterojunction has been formed between n-type MoS2 and p-type Bi-doped TiO2, which provides a potential gradient to increase charge separation and transfer efficiency. On the basis of these experimental results, this enhanced photocatalytic activity of MoS2/Bi-TiO2 heterostructures could be ascribed to the significant visible light absorption and the efficient charge carrier separation. Thus, this work demonstrates the effect of p-n junction for achieving high H-2 evolution activity and photoelectrochemical water oxidation under visible light illumination.
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页数:12
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