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    BiFeO3/TiO2 nanotube arrays composite electrode: Construction, characterization, and enhanced photoelectrochemical properties

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    Fulltext not available
    Authors
    Zhu, A.
    Zhao, Q.
    Li, Xin Yong
    Shi, Y.
    Date
    2014
    Type
    Journal Article
    
    Metadata
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    Citation
    Zhu, A. and Zhao, Q. and Li, X.Y. and Shi, Y. 2014. BiFeO3/TiO2 nanotube arrays composite electrode: Construction, characterization, and enhanced photoelectrochemical properties. ACS Applied Materials and Interfaces. 6 (1): pp. 671-679.
    Source Title
    ACS Applied Materials and Interfaces
    DOI
    10.1021/am404774z
    ISSN
    1944-8244
    School
    Department of Chemical Engineering
    URI
    http://hdl.handle.net/20.500.11937/47743
    Collection
    • Curtin Research Publications
    Abstract

    This work aims at the exploration of nanostructured ferroelectric-material-modified semiconductor electrodes for enhanced photo-induced activity. A well-aligned BiFeO3/TiO2-nanotubes (NTs) array with visible-light activity was successfully synthesized on a titanium sheet by combining anodization and an ultrasonic-immersion method followed by annealing. The structural and optical properties of the TiO2-NTs and the composite BiFeO3/TiO2-NTs were comparatively characterized. The composite BiFeO3/TiO2-NTs grown on a Ti sheet and used as an electrode exhibited a stronger absorption in the visible region and a much higher photoconversion efficiency than the pure TiO2-NTs/Ti electrode. Electrochemical impedance investigation attested to a significant improvement of the interfacial electron-transfer kinetics with enhanced separation of electron-hole pairs. The as-prepared composite electrode showed a high efficiency for photoelectrocatalytic degradation towards rhodamine B under visible-light irradiation (λ > 400 nm). The enhanced photoelectrocatalytic activity of the composite electrode could be attributed to the synergistic effect between the lowered electron-hole recombination rate by the applied bias and the wider spectral response promoted by the BiFeO3 component.

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