Facile fabrication of three-dimensional interconnected nanoporous N-TiO2 for efficient photoelectrochemical water splitting

被引:60
作者
Chen, Yingzhi [1 ]
Li, Aoxiang [1 ]
Li, Qun [2 ]
Hou, Xinmei [2 ]
Wang, Lu-Ning [1 ,3 ]
Huang, Zheng-Hong [4 ]
机构
[1] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
[2] Univ Sci & Technol Beijing, Sch Met & Ecol Engn, Beijing 100083, Peoples R China
[3] Univ Sci & Technol Beijing, State Key Lab Adv Met & Mat, Beijing 100083, Peoples R China
[4] Tsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat MOE, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
3D interconnected nanoporous N-TiO2; N-TiO2 nanotube arrays; Anodization; Photoelectrochemical water splitting; ENHANCED PHOTOCATALYTIC ACTIVITY; VISIBLE-LIGHT PHOTOCATALYSIS; GRAPHITIC CARBON NITRIDE; HYDROGEN EVOLUTION; GRAPHENE OXIDE; TIO2; ARRAYS; ACTIVATION; NANOTUBES; OXIDATION;
D O I
10.1016/j.jmst.2017.07.010
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Three-dimensional (3D) interconnected porous architectures are expected to perform well in photoelectrochemical (PEC) water splitting due to their high specific surface area as well as favourable porous properties and interconnections. In this work, we demonstrated the facile fabrication of 3D interconnected nanoporous N-doped TiO2 (N-TiO2 network) by annealing the anodized 3D interconnected nanoporous TiO2 (TiO2 network) in ammonia atmosphere. The obtained N-TiO2 network exhibited broadened light absorption, and abundant, interconnected pores for improving charge separation, which was supported by the reduced charge transfer resistance. With these merits, a remarkably high photocurrent density at 1.23 V vs. reversible hydrogen electrode (RHE) was realized for the N-TiO2 network without any co-catalysts or sacrificial reagents, and the photostability can be assured after long term illumination. In view of its simplicity and efficiency, this structure promises for perspective PEC applications. (C) 2017 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
引用
收藏
页码:955 / 960
页数:6
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