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Authors

Cheng GONG, State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian Province, China;Shenzhen Research Institute of Xiamen University, Shenzhen 518000, China;Fujian Provincial Key Laboratory of Featured Materials in Biochemical Industry, Ningde Normal University, Ningde 352100, Fujian Province, China;
Ze-yang ZHANG, State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian Province, China;
Si-wan XIANG, State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian Province, China;Shenzhen Research Institute of Xiamen University, Shenzhen 518000, China;Fujian Provincial Key Laboratory of Featured Materials in Biochemical Industry, Ningde Normal University, Ningde 352100, Fujian Province, China;
Lan SUN, State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian Province, China;Shenzhen Research Institute of Xiamen University, Shenzhen 518000, China;Fujian Provincial Key Laboratory of Featured Materials in Biochemical Industry, Ningde Normal University, Ningde 352100, Fujian Province, China;
Chen-qing YE, Fujian Provincial Key Laboratory of Featured Materials in Biochemical Industry, Ningde Normal University, Ningde 352100, Fujian Province, China;
Chang-jian LIN, State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian Province, China;

Corresponding Author

Lan SUN(sunlan@xmu.edu.cn)

Abstract

The LaNiO3/TiO2 nanotube arrays were prepared by pulse electrodeposition combined with high temperature annealing. The LaNiO3 nanoparticles modified on the TiO2 nanotube arrays had small particle size (< 10 nm), uniform distribution and controllable loading. Some LaNiO3 nanoparticles were deposited inside the TiO2 nanotubes. The UV-visible absorption spectra displayed that the absorption band edge of LaNiO3/TiO2 nanotube arrays was obviously red-shifted as compared with that of TiO2 nanotube arrays, and the visible light absorption was enhanced significantly. The photocatalytic degradation results of rhodamine B (RhB) under visible light showed that the LaNiO3/TiO2 nanotube arrays prepared by pulse electrodeposition for 500 cycles had the optimum photocatalytic activity, and the photocatalytic degradation rate of RhB was 3.5 times that of TiO2 nanotube arrays. Furthermore, the LaNiO3/TiO2 nanotube arrays presented the excellent photocatalytic stability.

Graphical Abstract

Keywords

LaNiO3 nanoparticles, TiO2 nanotube arrays, visible-light-induced photocatalysis, rhodamine B

Publication Date

2019-12-28

Online Available Date

2019-01-28

Revised Date

2019-01-08

Received Date

2018-12-12

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