2D MOFs enriched g-C3N4 nanosheets for highly efficient charge separation and photocatalytic hydrogen evolution from water

被引:63
作者
Liang, Yinghua [1 ]
Shang, Rong [1 ]
Lu, Jinrong [1 ]
An, Weijia [1 ]
Hu, Jinshan [1 ]
Liu, Li [1 ]
Cui, Wenquan [1 ]
机构
[1] North China Univ Sci & Technol, Coll Chem Engn, Hebei Key Lab Environm Photocatalyt & Electrocata, Tangshan 063210, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
2D-2D heterostructure; g-C3N4; UMOFNs; Photocatalyst; H-2; evolution; GRAPHITIC CARBON NITRIDE; METAL-ORGANIC FRAMEWORKS; PHOTOELECTROCATALYTIC DEGRADATION; ARTIFICIAL PHOTOSYNTHESIS; H-2; EVOLUTION; BISPHENOL-A; Z-SCHEME; TIO2; HETEROJUNCTIONS; SEMICONDUCTORS;
D O I
10.1016/j.ijhydene.2018.12.036
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
Here we report a 2D-2D heterostructure of g-C3N4/UMOFNs photocatalysts via mechanical grinding two kinds of two-dimensional nanosheets of g-C3N4 nanosheets and UMOFNs, which exhibits enhanced H2 evolution from water with simulated solar irradiation. g-C3N4 nanosheets are in close contact with UMOFNs, and there is a certain interaction between them, showing the effect of superimposition on the two-dimensional layer. The 2D-2D heterostructure offers a maximal photocatalytic hydrogen production activity of 1909.02 mu mol g(-1) h(-1) with 3 wt% of UMOFNs, which is 3-fold higher than that of g-C3N4 nanosheets (628.76 mu mol g(-1) h(-1)) and 15-flod higher than that of bulk g-C3N4 (124.30 mu mol g(-1)) The significant increasement of photocatalysis is due to 2D-2D heterostructure possessing a short charge transfer distance and large contact area between g-C3N4 and UMOFNs. The highly dispersed Ni-O, Co-O and pi-pi bonds in UMOFNs of 2D-2D structure also promote charge transfer and enhance the photocatalytic activity. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2797 / 2810
页数:14
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