4.6 Article

Electrochemically Self-Doped TiO2 Nanotube Arrays for Efficient Visible Light Photoelectrocatalytic Degradation of Contaminants

期刊

ELECTROCHIMICA ACTA
卷 136, 期 -, 页码 310-317

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2014.05.091

关键词

TiO2 nanotube arrays; Self-doped; Photoelectrocatalytic activity; Electrical conductivity

资金

  1. Ministry of Science and Technology of China [2010DFA22770]
  2. International Science & Technology Cooperation Program of China [2013DFG50150]
  3. National Natural Science Foundation of China [51079056/E090301]
  4. fundamental research funds for the Central Universities HUST [2014TS094]

向作者/读者索取更多资源

In this study, a simple electrochemical reduction approach is reported to enhance the photoelectrochemical performance of TiO2 nanotube arrays towards degrading water contaminants such as Rhodamine B, phenol and E. coli K-12. The results obtained from X-ray diffraction and X-ray photoelectron spectroscopy demonstrate that oxygen vacancies i.e., Ti3+ self-doping, were formed in the lattices of TiO2 nanotube arrays during the electrochemical reduction process of pristine TiO2 nanotube arrays at different negative potentials ranging from -1.2 to -1.5V. Comparing the pristine TiO2 nanotube arrays, the treatment TiO2 nanotube arrays samples by electroreduction process were found to be showing enhanced photoelectrocatalytic activity in the UV and visible regions in the entire potential window tested. Further, the photocurrent density of self-doped TiO2 nanotube arrays sample prepared at 1.3 V was 250% higher than that of the pristine TiO2 under visible-light illumination. Impedance analysis revealed that the electrical conductivity of the nanotubes significantly enhanced after self-doping. The photoelectrocatalytic activity of the self-doped TiO2 nanotube increased dramatically due to the enhanced electrical conductivity and absorption in the visible light region, as well as an accelerated charge transfer rate between the interface of solid and electrolyte. (C) 2014 Elsevier Ltd. All rights reserved.

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