Metal-free tellurene cocatalyst with tunable bandgap for enhanced photocatalytic hydrogen production

被引:29
|
作者
Qiu, B. [1 ,2 ,3 ]
Wang, C. [2 ,3 ]
Wang, J. [2 ,3 ]
Lin, Z. [2 ,3 ]
Zhang, N. [2 ,3 ]
Cai, L. [2 ,3 ]
Tao, X. [4 ]
Chai, Y. [2 ,3 ]
机构
[1] Nanjing Agr Univ, Coll Sci, Dept Chem, Jiangsu Key Lab Pesticide Sci, Nanjing 210095, Peoples R China
[2] Hong Kong Polytech Univ, Dept Appl Phys, Hung Hom, Kowloon, Hong Kong 999077, Peoples R China
[3] Hong Kong Polytech Univ, Shenzhen Res Inst, Shenzhen 518057, Peoples R China
[4] Hong Kong Polytech Univ, Inst Text & Clothing, Hung Hom, Kowloon, Hong Kong 999077, Peoples R China
关键词
Photocatalysis; Electron capture; Band alignment; Metal-free cocatalysts; TOTAL-ENERGY CALCULATIONS; H-2; EVOLUTION; SEMICONDUCTOR; CO2; HETEROSTRUCTURE; TRANSITION; EFFICIENCY;
D O I
10.1016/j.mtener.2021.100720
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The discovery of metal-free elemental cocatalysts has spurred dramatic advances in the field of photocatalysis. Bandgap engineering has always been used as an effective approach to make these cocatalysts form favorable band alignment with photocatalysts. Here, we develop metal-free tellurene (Te) with largely tunable bandgap as a highly efficient cocatalyst and investigate its thickness-dependent catalytic activity. Our experimental and theoretical studies reveal that the increased reduction potential of conduction band together with the decreased thickness, abundant active sites, and high charge mobility of Te, as well as the strong electronic coupling effects between Te and metal sulfides enable the enhanced photocatalytic hydrogen evolution rate and high quantum efficiency of 11.4% under the light illumination with the wavelength of 420 nm. This work enriches our understanding of the structure-activity correlations for Te and opens a path for solar energy harvesting from artificial photosynthesis by robust and cost-effective photocatalysts. (c) 2021 Elsevier Ltd. All rights reserved.
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页数:8
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