Oxyhydroxide Nanosheets with Highly Efficient Electron-Hole Pair Separation for Hydrogen Evolution

被引:111
|
作者
Huang, Junheng [1 ]
Shang, Qichao [2 ]
Huang, Yuanyuan [1 ]
Tang, Fumin [1 ]
Zhang, Qun [2 ]
Liu, Qinghua [1 ]
Jiang, Shan [1 ]
Hu, Fengchun [1 ]
Liu, Wei [1 ]
Luo, Yi [2 ]
Yao, Tao [1 ]
Jiang, Yong [1 ]
Pan, Zhiyun [1 ]
Sun, Zhihu [1 ]
Wei, Shiqiang [1 ]
机构
[1] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
cobalt; hydrogen evolution; nanosheets; XAFS spectroscopy; WATER OXIDATION; PHOTOCATALYSIS; OXIDE; CATALYST; NANOMATERIALS; NANOCRYSTALS; ABSORPTION; CELLS;
D O I
10.1002/anie.201510642
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The facile electron-hole pair recombination in earth-abundant transition-metal oxides is a major limitation for the development of highly efficient hydrogen evolution photocatalysts. In this work, the thickness of a layered -CoOOH semiconductor that contains metal/hydroxy groups was reduced to obtain an atomically thin, two-dimensional nanostructure. Analysis by ultrafast transient absorption spectroscopy revealed that electron-hole recombination is almost suppressed in the as-prepared 1.3nm thick -CoOOH nanosheet, which leads to prominent electron-hole separation efficiencies of 60-90% upon irradiation at 350-450nm, which are ten times higher than those of the bulk counterpart. X-ray absorption spectroscopy and first-principles calculations demonstrate that [HO-CoO6-x] species on the nanosheet surface promote H+ adsorption and H-2 desorption. An aqueous suspension of the -CoOOH nanosheets exhibited a high hydrogen production rate of 160molg(-1)h(-1) even when the system was operated for hundreds of hours.
引用
收藏
页码:2137 / 2141
页数:5
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