Preparation and photocatalytic properties of graphene/TiO2 nanotube arrays photoelectrodes

被引:29
作者
Zhang, Qingzhe [1 ,2 ]
Bao, Nan [2 ]
Zhu, Xiangwei [1 ]
Ma, Dong [1 ]
Xin, Yanjun [1 ]
机构
[1] Qingdao Agr Univ, Coll Resource & Environm, Rural Environm Engn Ctr Qingdao, Qingdao 266109, Peoples R China
[2] Shandong Univ, Sch Environm Sci & Engn, Jinan 250100, 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
TiO2 nanotube arrays; Graphene; Electra-deposition; Photocatalysis; COMBUSTION SYNTHESIS; TIO2; WATER; OXIDE; DYE; DEGRADATION; FILMS; PHOTODEGRADATION; SEMICONDUCTOR; NANOCOMPOSITE;
D O I
10.1016/j.jallcom.2014.09.021
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
Graphene/TiO2 Nanotube Arrays (GR/TNAs) photoelectrodes were fabricated by in-situ anodization and electro-deposition method. The surface morphology, structure, photoluminescence spectra (PL), and photocatalytic activity of the samples were investigated. The as-prepared graphene/TNAs (GR/TNAs) photoelectrodes showed significant improvement in the separation of photogenerated carriers and excellent photocatalytic stability. The effects of irradiation time, initial concentration, ionic strength and bias potential on the removal of rhodamine B (Rh.B) by TNAs and GR/TNAs were studied. Results showed that degradation rate of Rh.B for GR/TNAs photoelectrodes reached 75% after 60 min illumination at pH of 6.0. The GR/TNAs exhibited significantly enhanced photocatalytic activity compared to unmodified TNAs. When the bias potential was applied, Rh.B degradation rate increased to 90% at 0.5 V. NO3-, Ca2+ and Mg2+ in the solution promoted the degradation of Rh.B, while SO42-, Cl- and F- suppressed the removal rate. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:761 / 767
页数:7
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