共 50 条
Single Tungsten Atoms Supported on MOF-Derived N-Doped Carbon for Robust Electrochemical Hydrogen Evolution
被引:522
|作者:
Chen, Wenxing
[1
,2
]
Pei, Jiajing
[3
,4
]
He, Chun-Ting
[5
]
Wan, Jiawei
[1
]
Ren, Hanlin
[1
]
Wang, Yu
[6
]
Dong, Juncai
[7
]
Wu, Konglin
[1
]
Cheong, Weng-Chon
[1
]
Mao, Junjie
[1
]
Zheng, Xusheng
[8
]
Yan, Wensheng
[8
]
Zhuang, Zhongbin
[3
,4
]
Chen, Chen
[1
]
Peng, Qing
[1
]
Wang, Dingsheng
[1
]
Li, Yadong
[1
]
机构:
[1] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[2] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing Key Lab Construct Tailorable Adv Funct Ma, Beijing 100081, Peoples R China
[3] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[4] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
[5] Sun Yat Sen Univ, Sch Chem, MOE Key Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Guangdong, Peoples R China
[6] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
[7] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[8] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
基金:
中国国家自然科学基金;
北京市自然科学基金;
关键词:
electrocatalysts;
hydrogen evolution reaction;
metal-organic frameworks;
N-doped carbon;
single W atoms;
METAL-ORGANIC FRAMEWORKS;
OXYGEN REDUCTION;
CARBIDE NANOPARTICLES;
EFFICIENT;
CONVERSION;
CATALYSTS;
ELECTROCATALYSTS;
GRAPHENE;
SITES;
ULTRASMALL;
D O I:
10.1002/adma.201800396
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Tungsten-based catalysts are promising candidates to generate hydrogen effectively. In this work, a single-W-atom catalyst supported on metal-organic framework (MOF)-derived N-doped carbon (W-SAC) for efficient electrochemical hydrogen evolution reaction (HER), with high activity and excellent stability is reported. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and X-ray absorption fine structure (XAFS) spectroscopy analysis indicate the atomic dispersion of the W species, and reveal that the W1N1C3 moiety may be the favored local structure for the W species. The W-SAC exhibits a low overpotential of 85 mV at a current density of 10 mA cm(-2) and a small Tafel slope of 53 mV dec(-1), in 0.1 m KOH solution. The HER activity of the W-SAC is almost equal to that of commercial Pt/C. Density functional theory (DFT) calculation suggests that the unique structure of the W1N1C3 moiety plays an important role in enhancing the HER performance. This work gives new insights into the investigation of efficient and practical W-based HER catalysts.
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