Cu oxide quantum dots loaded TiO2 nanosheet photocatalyst for highly efficient and robust hydrogen generation

被引:29
作者
Sadanandam, Gullapelli [1 ]
Luo, Xiao [1 ]
Chen, Xuxing [1 ]
Bao, Yuwen [1 ]
Homewood, Kevin Peter [1 ]
Gao, Yun [1 ]
机构
[1] Hubei Univ, Minist Educ, Key Lab Green Preparat & Applicat Funct Mat, Sch Mat Sci & Engn, Wuhan 430062, Peoples R China
基金
中国国家自然科学基金;
关键词
TiO2; nanosheets; Cu oxide quantum dot; Photocatalyst; H-2; generation; ANATASE TIO2; 001; FACETS; PERCENTAGE; DIOXIDE; NANOCOMPOSITES; COMPOSITE; EVOLUTION; ENHANCE; FILMS;
D O I
10.1016/j.apsusc.2020.148687
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
To simultaneously enhance both the hydrogen generation activity and long term stability of a TiO2 based photocatalyst using Cu species as co-catalyst is a great challenge. In this work, highly reactive TiO2 nanosheets with {0 0 1} facets were prepared by a hydrothermal method, and then Cu oxides quantum dot was loaded on the nanosheets by an impregnation method. Comprehensive analysis demonstrates that the Cu species change from CuO to Cu2O and partially to Cu during photocatalysis, and this process is reversed during oxidation. The exposed TiO2 (0 0 1) planes provide a platform for a strong interaction between the Cu oxide and TiO2 nanosheets, enabling the firmly anchor and charge transfer between the Cu oxide and TiO2. The optimized composite photocatalyst shows a high efficiency and robust, long term stability for H2 evolution. With simple O-2 regeneration, the H2 generation rate maintains to 98% after irradiation for 30 h. It is expected that TiO2 is sandwiched between TiO2 and CuO, and the composite configuration changes to TiO2/Cu2O/Cu after long term irradiation. The energy band alignment of the double heterojunction provides the effective charge separation and maintains the structural stability during the photocatalysis.
引用
收藏
页数:9
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