Hydrothermal fabrication of few-layer MoS2 nanosheets within nanopores on TiO2 derived from MIL-125(Ti) for efficient photocatalytic H2 evolution

被引:56
作者
Ye, Fei [1 ]
Li, Houfen [2 ]
Yu, Hongtao [1 ]
Chen, Shuo [1 ]
Quan, Xie [1 ]
机构
[1] Dalian Univ Technol, Key Lab Ind Ecol & Environm Engn, Minist Educ China, Sch Environm Sci & Technol, Dalian 116024, Peoples R China
[2] Taiyuan Univ Technol, Coll Environm Sci & Engn, Taiyuan 030024, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Porous TiO2; MoS(2 )nanosheets; Confined growth; Active edge sites; H-2; evolution; METAL-ORGANIC FRAMEWORKS; HYDROGEN-EVOLUTION; NANOSTRUCTURES; SULFIDE; WATER; TRANSITION; STATE; SITE;
D O I
10.1016/j.apsusc.2017.07.087
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
Protons tend to bond strongly with unsaturated-coordinate S element located at the edge of nano-MoS2 and are consequently reduced to H-2. Therefore, increasing the active S atoms quantity will be a feasible approach to enhance hydrogen evolution. Herein we developed a porous TiO2 derived from metal organic frameworks (MOFs) as scaffold to restrict the growth and inhibit the aggregation of MoS(2 )nanosheets. As a result, the thickness of the prepared MoS(2 )nanosheets was less than 3 nm (1-4 layers), with more edges and active S atoms being exposed. This few-layer MoS2-porous TiO2 exhibits a H-2 evolution rate of 897.5 1 mu mol h(-1) g(-1), which is nearly twice as much as free-stand MoS(2 )nanosheets and twenty times more than physical mixture of MoS(2 )with porous TiO2. The high performance is attributed to that more active edge sites in few-layer MoS2-porous TiO(2 )are exposed than pure MoS2. This work provides a new method to construct MOFs derived porous structures for controlling MoS2 to expose active sites for HER. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
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