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    陈硕

    • 教授     博士生导师   硕士生导师
    • 性别:女
    • 毕业院校:大连理工大学
    • 学位:博士
    • 所在单位:环境学院
    • 学科:环境工程. 环境科学
    • 办公地点:大连理工大学环境学院B717
    • 联系方式:0411-84706263
    • 电子邮箱:shuochen@dlut.edu.cn

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    Silicon nanowire/TiO2 heterojunction arrays for effective photoelectrocatalysis under simulated solar light irradiation

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    论文类型:期刊论文

    发表时间:2009-07-25

    发表刊物:APPLIED CATALYSIS B-ENVIRONMENTAL

    收录刊物:SCIE、EI

    卷号:90

    期号:1-2

    页面范围:242-248

    ISSN号:0926-3373

    关键字:Silicon nanowire (SiNW); TiO2; Photoelectrocatalysis; Heterojunction

    摘要:The silicon nanowire (SiNW)/TiO2 heterojunction arrays have been prepared by chemical vapor depositing a TiO2 layer on SiNW arrays which are obtained by chemical etching of Si wafers. The types of SiNW/TiO2 heterojunctions can be modulated simply by using p-type or n-type Si wafers. Compared with samples of depositing TiO2 on p-type or n-type Si wafers (p-Si/TiO2 or p-Si/TiO2), both n-SiNW/TiO2 and p-SiNW/TiO2 heterojunctions can improve the ultraviolet photoresponse under a bias potential, and in particular, a remarkable visible photoresponse of n-SiNW/TiO2 heterojunction is observed when the bias potential is higher than 1.7 V (vs. SCE). Cyclic voltammetry (CV) curves illuminate that n-SiNW/TiO2 heterojunctions have steady visible photoresponse in aqueous solution. According to the surface photovoltage (SPV) measurements, it is found that n-SiNW/TiO2 heterojunctions possess window effect, namely, n-SiNW/TiO2 heterojunctions can utilize the superposition photoresponse in the wavelength ranges from 300 to 400 nm (contributed by TiO2) and from 400 to 800 nm (contributed by n-SiNW). The mechanism of this phenomenon is explained based on the energy band model. The photoelectrocatalytic activity of the n-SiNW/TiO2 heterojunction arrays is evaluated using phenol as a test substance under Xe lamp irradiation. The kinetic constant and total organic carbon (TOC) removal are 1.7 times and 2 times as great as those of n-Si/TiO2, respectively. (C) 2009 Elsevier B.V. All rights reserved.