Building 2D/2D CdS/MOLs Heterojunctions for Efficient Photocatalytic Hydrogen Evolution

被引:64
|
作者
Yang, Wei [1 ]
Xu, Meng [1 ]
Tao, Ke-Ying [1 ]
Zhang, Ji-Hong [1 ]
Zhong, Di-Chang [1 ]
Lu, Tong-Bu [1 ]
机构
[1] Tianjin Univ Technol, Sch Mat Sci & Engn, Inst New Energy Mat & Low Carbon Technol, MOE Int Joint Lab Mat Microstruct, Tianjin 300384, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
2D; 2D heterostructures; metal-organic layers; photocatalytic hydrogen evolution; porous CdS nanosheets; LIGHT-DRIVEN PHOTOCATALYST; CDS; NANOPARTICLES; NANOSHEETS; WATER; MOFS;
D O I
10.1002/smll.202200332
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
2D lamellar materials can offer high surface area and abundant reactive sites, thus showing an appealing prospect in photocatalytic hydrogen evolution. However, it is still difficult to build cost-efficient photocatalytic hydrogen evolution systems based on 2D materials. Herein, an in situ growth method is employed to build 2D/2D heterojunctions, with which 2D Ni-based metal-organic layers (Ni-MOLs) are closely grown on 2D porous CdS (P-CdS) nanosheets, affording traditional P-CdS/Ni-MOL heterojunction materials. Impressively, the optimized P-CdS/Ni-MOL catalyst exhibits superior photocatalytic hydrogen evolution performance, with an H-2 yield of 29.81 mmol g(-1) h(-1). This value is 7 and 2981 times higher than that of P-CdS and Ni-MOLs, respectively, and comparable to those of reported state of the art catalysts. Photocatalytic mechanism studies reveal that the enhanced photocatalytic performance can be attributed to the 2D/2D intimate interface between P-CdS and Ni-MOLs, which facilitates the fast charge carriers' separation and transfer. This work provides a strategy to develop 2D MOL-based photocatalysts for sustainable energy conversion.
引用
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页数:8
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