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dc.contributor.authorCheng, Hsyi-Enen_US
dc.contributor.authorHung, Chi-Hsiuen_US
dc.contributor.authorYu, Ing-Songen_US
dc.contributor.authorYang, Zu-Poen_US
dc.date.accessioned2019-04-02T05:59:54Z-
dc.date.available2019-04-02T05:59:54Z-
dc.date.issued2018-10-01en_US
dc.identifier.issn2073-4344en_US
dc.identifier.urihttp://dx.doi.org/10.3390/catal8100440en_US
dc.identifier.urihttp://hdl.handle.net/11536/148374-
dc.description.abstractThe photocatalysts of immobilized TiO(2 )film suffer from high carrier recombination loss when compared to its powder form. Although the TiO2 with rutile-anatase mixed phases has higher carrier separation efficiency than those with pure anatase or rutile phase, the single junction of anatase/rutile cannot avoid the recombination of separated carriers at the interface. In this study, we propose a TiO2/SnO2/Ni multi-heterojunction structure which incorporates both Schottky contact and staggered band alignment to reduce the carrier recombination loss. The low carrier recombination rate of TiO2 film in TiO2/SnO2/Ni multi-heterojunction structure was verified by its low photoluminescence intensity. The faster degradation of methylene blue for TiO2 /SnO2/Ni multi-junctions than for the other fabricated structures, which means that the TiO2 films grown on the SnO2/Ni/Ti coated glass have a much higher photocatalytic activity than those grown on the blank glass, SnO2-coated and Ni/Ti-coated glasses, demonstrated its higher performance of photogenerated carrier separation.en_US
dc.language.isoen_USen_US
dc.subjectmultijunctionen_US
dc.subjecttitanium dioxideen_US
dc.subjectthin filmen_US
dc.subjectphotocatalysisen_US
dc.subjectfunctional coatingsen_US
dc.titleStrongly Enhancing Photocatalytic Activity of TiO2 Thin Films by Multi-Heterojunction Techniqueen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/catal8100440en_US
dc.identifier.journalCATALYSTSen_US
dc.citation.volume8en_US
dc.contributor.department光電系統研究所zh_TW
dc.contributor.departmentInstitute of Photonic Systemen_US
dc.identifier.wosnumberWOS:000448543300036en_US
dc.citation.woscount0en_US
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