Activating MoS2 for pH-Universal Hydrogen Evolution Catalysis

被引:187
作者
Li, Guoqing [1 ]
Zhang, Du [2 ]
Yu, Yifei [1 ]
Huang, Shengyang [3 ]
Yang, Weitao [2 ]
Cao, Linyou [1 ,4 ,5 ]
机构
[1] North Carolina State Univ, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
[2] Duke Univ, Dept Chem, Durham, NC 27708 USA
[3] North Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
[4] North Carolina State Univ, Dept Phys, Raleigh, NC 27695 USA
[5] North Carolina State Univ, Dept Elect & Comp Engn, Raleigh, NC 27695 USA
基金
美国国家科学基金会;
关键词
ACTIVE EDGE SITES; MONOLAYER MOS2; NANOSHEETS; LAYER; PHOTOLUMINESCENCE; EFFICIENT; FILMS; WS2;
D O I
10.1021/jacs.7b07450
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
MoS2 presents a promising catalyst for the hydrogen evolution reaction (HER) in water splitting, but its worse catalytic performance in neutral and alkaline media than in acidic environment may be problematic for practical application. This is because the other half reaction of water splitting, i.e., oxygen evolution reaction, often needs to be implemented in alkaline environment. Here we demonstrate a universal strategy that may be used to significantly improve the HER catalysis of MoS2 in all kinds of environments from acidic to alkaline, proton intercalation. Protons may be enabled to intercalate between monolayer MoS2 and underlying substrates or in the interlayer space of thicker MoS2 by two processes: electrochemically polarizing MoS2 at negative potentials (vs RHE) in acidic media or immersing MoS2 into certain acid solutions like TFSI. The improvement in catalytic performance is due to the activity enhancement of the active sites in MoS2 by the intercalated protons, which might be related with the effect of the intercalated protons on electrical conductance and the adsorption energy of hydrogen atoms. The enhancement in catalytic activity by the intercalated proton is very stable even in neutral and alkaline electrolytes.
引用
收藏
页码:16194 / 16200
页数:7
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