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    • 教授     博士生导师   硕士生导师
    • 性别:男
    • 毕业院校:奥地利University of Graz
    • 学位:博士
    • 所在单位:环境学院
    • 学科:环境工程. 环境科学. 水科学与技术
    • 办公地点:大连理工大学环境学院
    • 联系方式:0411-84706140
    • 电子邮箱:quanxie@dlut.edu.cn

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    A silicon-doped TiO2 nanotube arrays electrode with enhanced photoelectrocatalytic activity

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    论文类型:期刊论文

    发表时间:2008-12-30

    发表刊物:APPLIED SURFACE SCIENCE

    收录刊物:SCIE、EI、Scopus

    卷号:255

    期号:5

    页面范围:2167-2172

    ISSN号:0169-4332

    关键字:Titanium dioxide; Nanotube; Silicon; Doped; Photoelectrochemical capability

    摘要:Silicon-doped titania nanotube arrays were fabricated by electrochemical anodization on a Ti sheet, followed by chemical vapor deposition (CVD) treatment using tetraethylorthosilicate as silicon source. The highly ordered nanotube arrays obtained by anodization kept its nanotube-like structural integrity after CVD treatment. X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) results revealed that the introduced silicon might be incorporated into titania matrix. This incorporation helped to increase the thermal stability of titania, which was in favor of suppressing the phase transformation from anatase into rutile and also inhibiting the growth of anatase crystallite of titania at high calcination temperature. A significant blue-shift was observed in the spectrum of UV absorption. The surface of Si-doped TiO2 nanotube arrays showed a super-hydrophilic behavior under UV illumination. For Si-doped TiO2 nanotube electrode, the maximum photoconversion efficiencies of 31.8% under high-pressure mercury lamp irradiation and 16.5% using an optical. filter (280-400 nm) under the same lamp irradiation were achieved, which were obviously higher than those of undoped one. The photoelectrocatalytic (PEC) activities were investigated using pentachlorophenol (PCP) as a probe substance. Compared with undoped TiO2 nanotube electrode, the Si-doped TiO2 showed better PEC capability in the degradation of PCP under high-pressure mercury lamp irradiation. (C) 2008 Elsevier B. V. All rights reserved.