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In Situ Formation of Disorder-Engineered TiO2(B)-Anatase Heterophase Junction for Enhanced Photocatalytic Hydrogen Evolution
被引:120
作者:
Cai, Jinmeng
[1
]
Wang, Yating
[1
]
Zhu, Yingming
[1
]
Wu, Moqing
[1
]
Zhang, Hao
[1
]
Li, Xingang
[1
]
Jiang, Zheng
[2
]
Meng, Ming
[1
]
机构:
[1] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin Key Lab Appl Catalysis Sci & Engn, Sch Chem Engn & Technol, Tianjin 30072, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
基金:
中国国家自然科学基金;
关键词:
hydrogenation;
TiO2(B);
heterophase junction;
photocatalytic;
water splitting;
TITANIUM-DIOXIDE;
BLACK TIO2;
NANOPARTICLES;
ABSORPTION;
NANOWIRES;
WATER;
D O I:
10.1021/acsami.5b07318
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Hydrogenation of semiconductors is an efficient way to increase their photocatalytic activity by forming disorder-engineered structures. Herein, we report a facile hydrogenation process of TiO2(B) nanobelts to in situ generate TiO2(B)-anatase heterophase junction with a disordered surface shell. The catalyst exhibits an excellent performance for photocatalytic hydrogen evolution under the simulated solar light irradiation (similar to 580 mu mol h(-1), 0.02 g photocatalyst). The atomically well-matched heterophase junction, along with the disorder-engineered surface shell, promotes the separation of electron-hole and inhibits their recombination. This strategy can be further employed to design other disorder-engineered composite photocatalysts for solar energy utilization.
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页码:24987 / 24992
页数:6
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