| Literature DB >> 26732536 |
Junheng Huang1, Qichao Shang2, Yuanyuan Huang1, Fumin Tang1, Qun Zhang2, Qinghua Liu3, Shan Jiang1, Fengchun Hu1, Wei Liu1, Yi Luo2, Tao Yao4, Yong Jiang1, Zhiyun Pan1, Zhihu Sun1, Shiqiang Wei5.
Abstract
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 β-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 1.3 nm thick β-CoOOH nanosheet, which leads to prominent electron-hole separation efficiencies of 60-90 % upon irradiation at 350-450 nm, 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 H2 desorption. An aqueous suspension of the β-CoOOH nanosheets exhibited a high hydrogen production rate of 160 μmol g(-1) h(-1) even when the system was operated for hundreds of hours.Entities:
Keywords: XAFS spectroscopy; cobalt; hydrogen evolution; nanosheets
Year: 2016 PMID: 26732536 DOI: 10.1002/anie.201510642
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336