Photoeletrocatalytic activity of a Cu 2O-loaded self-organized highly oriented TiO 2 nanotube array electrode for 4-chlorophenol degradation
Differently sized Cu 2O nanoparticles have been assembled photocatalytically on the surface of self-organized highly oriented TiO 2 nanotubes obtained by anodization of a Ti sheet in fluoride- containing electrolytes. X-ray diffraction analysis identifies an anatase structure and fine preferential o...
| Main Authors: | , , , , |
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| Format: | Journal Article |
| Published: |
American Chemical Society
2009
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| Online Access: | http://hdl.handle.net/20.500.11937/23722 |
| Summary: | Differently sized Cu 2O nanoparticles have been assembled photocatalytically on the surface of self-organized highly oriented TiO 2 nanotubes obtained by anodization of a Ti sheet in fluoride- containing electrolytes. X-ray diffraction analysis identifies an anatase structure and fine preferential orientation of (101) planes. The UV-vis absorption edge of the TiO 2 nanotube arrays shift to lower energy after Cu 2O loading. The composite array electrode exhibits a higher photovoltage response than the TiO 2 powders directly deposited on a Ti sheet. The highest photoconversion efficiencies observed for the Cu 2O-loaded electrode are 17.2% and 0.82% under UV light and visible light irradiation, respectively. Especially, the composite array electrode shows a higher efficiency than the nonloaded one for the photoelectrocatalytic decomposition of 4-chlorophenol. The improved photoeletrocatalytic activity of the TiO 2/Cu 2O composite array electrode is attributed to the synergistic effect of Cu 2O nanoparticles and TiO 2 nanotube arrays. The Cu 2O nanoparticles could enhance the efficiency of photon harvesting and reduce the chances of electron-hole recombination by sending the electrons to the conduction band of TiO 2 nanotubes. The accumulated electrons in the conduction band of TiO 2 nanotubes would reduce oxygen to form peroxides for enhanced advanced oxidation. The byproducts were identified by high- performance liquid chromatography. © 2009 American Chemical Society. |
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