Sulfur-Depleted Monolayered Molybdenum Disulfide Nanocrystals for Superelectrochemical Hydrogen Evolution Reaction

被引:146
作者
Lin, Liangxu [1 ,2 ]
Miao, Naihua [3 ,4 ,5 ]
Wen, Yan [1 ]
Zhang, Shaowei [1 ]
Ghosez, Philippe [3 ]
Sun, Zhimei [4 ,5 ]
Allwood, Dan A. [2 ]
机构
[1] Univ Exeter, Coll Engn Math & Phys Sci, Exeter EX4 4QL, Devon, England
[2] Univ Sheffield, Dept Mat Sci & Engn, Sheffield S1 3JD, S Yorkshire, England
[3] Univ Liege, Inst Phys, Theoret Mat Phys, B-4000 Liege, Belgium
[4] Beihang Univ, Ctr Integrated Computat Mat Engn, Beijing 100191, Peoples R China
[5] Beihang Univ, Sch Mat Sci & Engn, Beijing 100191, Peoples R China
基金
英国工程与自然科学研究理事会;
关键词
monolayered molybdenum disulfide; nanocrystals; hydrogen evolution reaction; electrochemical; ACTIVE EDGE SITES; MOS2 ULTRATHIN NANOSHEETS; LAYER MOS2; PERFORMANCE; GRAPHENE; CATALYST; SURFACE;
D O I
10.1021/acsnano.6b04904
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalytically driven electrochemical hydrogen evolution reaction (HER) of monolayered molybdenum disulfide (MoS2) is usually highly suppressed by the scarcity of edges and low electrical conductivity. Here, we show how the catalytic performance of MoS2 monolayers can be improved dramatically by catalyst size reduction and surface sulfur (S) depletion. Monolayered MoS2 nanocrystals (NCs) (2-25 nm) produced via exfoliating and disintegrating their bulk,counterparts showed improved catalysis rates over monolayer sheets because of their increased edge ratios and metallicity. Subsequent S depletion of these NCs further improved the metallicity and made Mo atoms on the basal plane become catalytically active. As a result, the S-depleted NCs with low mass (similar to 1.2 mu g) showed super high catalytic performance on HER with a low Tafel slope of similar to 29 mV/decade, overpotentials of 60-75 mV, and high current densities j(x) (where x is in mV) of j(150) = 9.64 mA.cm(-2) and j(200) = 52.13 mA.cm(-2). We have found that higher production rates of H-2, could not be achieved by adding more NC layers since HER only happens on the topmost surface and the charge mobility decreases dramatically. These difficulties can be largely alleviated by creating a hybrid structure of NCs immobilized onto three-dimensional graphene to provide a very high surface exposure of the catalyst for electrochemical HER, resulting in very high current densities of j(150) = 49.5 mA.cm(-2) and j(200) = 232 mA.cm(-2) with similar to 44.3 mu g of NCs. Our experimental and theoretical studies show how careful design and modification of nanoscale materials/structures can result in highly efficient catalysis. There may be considerable opportunities in the broader family of transition metal dichalcogenides beyond just MoS2 to develop highly efficient atomically thin catalysts. These could offer cheap and effective replacement of precious metal catalysts in clean energy production.
引用
收藏
页码:8929 / 8937
页数:9
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