Influences of TiO2 phase structures on the structures and photocatalytic hydrogen production of CuOx/TiO2 photocatalysts

被引:65
|
作者
Liu, Yuanxu
Wang, Zhonglei
Huang, Weixin [1 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Mat Energy Convers, Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Heterojunction; Surface phase junction; Cu2O; Charge separation; Charge-participated surface reaction; LIQUID-PHASE; CATALYSTS; NANOPARTICLES; EFFICIENT; CUO; TRANSFORMATION; NANOSYSTEMS; GENERATION; REDUCTION; OXIDATION;
D O I
10.1016/j.apsusc.2016.07.173
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
CuOx/TiO2 photocatalysts employing TiO2 with different phase structures as well as P25 as supports were prepared, and their structures and activity for photocatalytic H-2 production in methanol/water solution under simulated solar light were comparatively studied. Structural characterization results demonstrated that the TiO2 phase structure strongly affects the CuOx-TiO2 interaction and copper species in various CuOx/TiO2 photocatalysts. The Cu2O-rutile TiO2 interaction is much stronger than the Cu2O-anatase TiO2 interaction, facilitates the interfacial charge transfer process within the Cu2O-rutile TiO2 heterojunction but disables supported Cu2O to catalyze the hole-participated methanol oxidation. The Cu2O-anatase TiO2 heterojunction with the appropriate Cu2O-anatase TiO2 interaction and thus the balancing efficiencies between the interfacial charge transfer process and hole-participated methanol oxidation is most photocatalytic active, and CuOx/P25 with the largest population of Cu2O-anatase TiO2 heterojunction exhibits the highest photocatalytic H-2 production. These results provide novel insights in the applied surface science of CuOx/TiO2 photocatalysts. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:760 / 767
页数:8
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