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dc.contributor.authorChen, Chien-Chonen_US
dc.contributor.authorLin, Jin-Shyongen_US
dc.contributor.authorDiau, Eric Wei-Guangen_US
dc.contributor.authorLiu, Tzeng-Fengen_US
dc.date.accessioned2014-12-08T15:42:56Z-
dc.date.available2014-12-08T15:42:56Z-
dc.date.issued2008-08-01en_US
dc.identifier.issn0947-8396en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s00339-008-4546-7en_US
dc.identifier.urihttp://hdl.handle.net/11536/29087-
dc.description.abstractSelf-cleaning of a surface of nanotube arrays of anodic titanium oxide (ATO) is demonstrated. The ATO was prepared in fluoride ion containing sulfate electrolytes with a structure of 0.4 mu m length, 100 nm pores diameter, 120 nm interpore distance, 25 nm pore wall thickness, a 8x10(9) pores cm(-2) pore density, and 68.2% porosity. Prepared as thin films either directly from a Ti foil or on a glass substrate, these arrays have the property that water drops spread quickly over the surface of the films without irradiation. In contrast, a flat anatase TiO2 film requires irradiation with UV light for several minutes before the contact angle decreases to zero. The observed self-cleaning behavior of the ATO thin films is due to the capillary effect of the nanochannel structure and the superhydrophilic property of the anatase TiO2 surface inside the tube.en_US
dc.language.isoen_USen_US
dc.titleSelf-cleaning characteristics on a thin-film surface with nanotube arrays of anodic titanium oxideen_US
dc.typeArticle; Proceedings Paperen_US
dc.identifier.doi10.1007/s00339-008-4546-7en_US
dc.identifier.journalAPPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSINGen_US
dc.citation.volume92en_US
dc.citation.issue3en_US
dc.citation.spage615en_US
dc.citation.epage620en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000257912000027-
Appears in Collections:Conferences Paper


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