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dc.contributor.authorHsu, Ming-Yien_US
dc.contributor.authorHsu, Hsin-Lingen_US
dc.contributor.authorLeu, Jihperngen_US
dc.date.accessioned2014-12-08T15:24:28Z-
dc.date.available2014-12-08T15:24:28Z-
dc.date.issued2012en_US
dc.identifier.issn0013-4651en_US
dc.identifier.urihttp://hdl.handle.net/11536/16975-
dc.identifier.urihttp://dx.doi.org/10.1149/2.063208jesen_US
dc.description.abstractTiO2 nanowires connected directly with TiO2 nanotubes arrays (TNWs/TNAs) were successfully fabricated with a mixture of ethylene glycol and water that contained NH4F electrolyte via a one-step method without mechanical stirring. The morphology of the TNWs/TNAs structure was investigated by changing the anodizing voltage and processing time to elucidate its formation mechanism. Well-developed anodic oxide nanowires are only observed under specific anodizing voltage and processing time conditions. The evolution of TNWs follows four stages: (1) thinning of the tube wall thickness with high roughness near the TNA mouths, (2) forming strings of through holes in the upper section of the TNAs, (3) splitting into nanowires, and (4) collapsing and further thinning of nanowires. For photocatalytic application, TNWs/TNAs film demonstrated a better photocatalytic performance than regular TNAs due to higher surface area predominantly and improved charge transport. Moreover, TNWs/TNAs film (20 nm wire/40 nm pore diameter) achieved a performance comparable to that of the film made from TiO2 nanoparticles. (C) 2012 The Electrochemical Society. [DOI: 10.1149/2.063208jes] All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleTiO2 Nanowires on Anodic TiO2 Nanotube Arrays (TNWs/TNAs): Formation Mechanism and Photocatalytic Performanceen_US
dc.typeArticleen_US
dc.identifier.doi10.1149/2.063208jesen_US
dc.identifier.journalJOURNAL OF THE ELECTROCHEMICAL SOCIETYen_US
dc.citation.volume159en_US
dc.citation.issue8en_US
dc.citation.spageH722en_US
dc.citation.epageH727en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000308559400083-
dc.citation.woscount2-
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