Solar-Light-Driven Pure Water Splitting with Ultrathin BiOCl Nanosheets

被引:110
作者
Zhang, Ling [1 ]
Han, Zhongkang [2 ,3 ]
Wang, Wenzhong [1 ]
Li, Xiaoman [1 ]
Su, Yang [1 ]
Jiang, Dong [1 ]
Lei, Xiaoling [2 ,3 ]
Sun, Songmei [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Div Interfacial Water, Shanghai 200050, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Appl Phys, Key Lab Interfacial Phys & Technol, Shanghai 200050, Peoples R China
基金
中国国家自然科学基金;
关键词
charge-carrier separation; nanosheets; photocatalysts; solar energy; water splitting; MOLECULAR-OXYGEN ACTIVATION; PHOTOCATALYTIC ACTIVITY; ELECTRONIC-STRUCTURE; BLACK TIO2; HYDROGEN; VACANCIES; BIVO4; OXIDE; ABSORPTION; SEPARATION;
D O I
10.1002/chem.201503778
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A suitable photocatalyst for overall water splitting has been produced by overcoming the disadvantage of the band structure in bulk BiOCl by reducing the thickness to the quantum scale. The ultrathin BiOCl nanosheets with surface/subsurface defects realized the solar-driven pure water splitting in the absence of any co-catalysts or sacrificial agent. These surface defects cannot only shift both the valence band and conduction band upwards for band-gap narrowing but also promote charge-carrier separation. The amount of defects in the outer layer surface of BiOCl results in an enhancement of carrier density and faster charge transport. First-principles calculations provide clear evidence that the formation of surface oxygen vacancies is easier for the ultrathin BiOCl nanosheets than for its thicker counterpart. These defects can serve as active sites to effectively adsorb and dissociate H2O molecules, resulting in a significantly improved water-splitting performance.
引用
收藏
页码:18089 / 18094
页数:6
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