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dc.contributor.authorZhu, A.
dc.contributor.authorZhao, Q.
dc.contributor.authorLi, Xin Yong
dc.contributor.authorShi, Y.
dc.date.accessioned2017-01-30T15:35:26Z
dc.date.available2017-01-30T15:35:26Z
dc.date.created2015-10-29T04:09:38Z
dc.date.issued2014
dc.identifier.citationZhu, 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.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/47743
dc.identifier.doi10.1021/am404774z
dc.description.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.

dc.titleBiFeO3/TiO2 nanotube arrays composite electrode: Construction, characterization, and enhanced photoelectrochemical properties
dc.typeJournal Article
dcterms.source.volume6
dcterms.source.number1
dcterms.source.startPage671
dcterms.source.endPage679
dcterms.source.issn1944-8244
dcterms.source.titleACS Applied Materials and Interfaces
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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