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

材料科学 可见光谱 光电流 兴奋剂 光催化 X射线光电子能谱 介电谱 化学工程 电化学 罗丹明B 电极 纳米技术 纳米管 碳纳米管 光电子学 化学 有机化学 催化作用 物理化学 工程类
作者
Wenjuan Liao,Jingwei Yang,He Zhou,Muthu Murugananthan,Yanrong Zhang
出处
期刊:Electrochimica Acta [Elsevier BV]
卷期号:136: 310-317 被引量:107
标识
DOI:10.1016/j.electacta.2014.05.091
摘要

• Self-doped TNTs photocatalyst is prepared by electrochemical reduction. • Self-doped TNTs photoelectrodes show an enhanced photoelectrochemical activity. • Self-doping can enhance both the absorption in visible region and electrical conductivity of the TNTs. • Self-doping can decrease the R ct between the solid-electrolyte interface. In this study, a simple electrochemical reduction approach is reported to enhance the photoelectrochemical performance of TiO 2 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., Ti 3+ self-doping, were formed in the lattices of TiO 2 nanotube arrays during the electrochemical reduction process of pristine TiO 2 nanotube arrays at different negative potentials ranging from −1.2 to −1.5 V. Comparing the pristine TiO 2 nanotube arrays, the treatment TiO 2 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 TiO 2 nanotube arrays sample prepared at −1.3 V was 250% higher than that of the pristine TiO 2 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 TiO 2 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.
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