In-situ wet tearing based subnanometer MoSeS for efficient hydrogen evolution

被引:8
作者
Lu, Wenli [1 ]
Cui, Jiabin [1 ]
Jiang, Rui [1 ]
Chen, Yueguang [1 ]
Wang, Leyu [1 ]
机构
[1] Beijing Univ Chem Technol, Beijing Key Lab Environm Harmful Chem Anal, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
subnanometer; transition-metal dichalcogenides; in-situ tearing; hydrogen evolution reaction; ACTIVE EDGE SITES; ULTRATHIN NANOSHEETS; GRAPHENE; NANOPARTICLES; CATALYST; HYBRID; ELECTROCATALYST; OXIDATION; DISULFIDE; PLATINUM;
D O I
10.1007/s40843-017-9112-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The development of ultrasmall transition-metal dichalcogenide (such as MoS2, MoSe2) nanostructures is an efficient strategy to increase the active edge sites and overall performance for hydrogen evolution reaction. Here, we report an in-situ tearing strategy to produce the carbon nanotube supported subnanometer ternary MoSeS (denoted as CNTs@NiSe@MoSeS) for efficient hydrogen evolution. Large (18.3 +/- 1.1 nm in length) multilayer MoS2 sheets grown on Ni (OH)(2) thin film are torn into subnanometer (5.2 +/- 0.7 nm in length) MoSeS via a subsequent selenization progress, along with the transformation of Ni(OH)(2) thin film into small NiSe nanoplates. The resulting nanocomposite exhibits abundant active edge sites, outstanding 10,000-cycle stability and ultrahigh activity with a low overpotential of 189 mV at a high current density of 200 mA cm(-2) toward hydrogen evolution.
引用
收藏
页码:929 / 936
页数:8
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