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.
引用
收藏
页码:24987 / 24992
页数:6
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