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dc.contributor.authorJang, Wei-Luenen_US
dc.contributor.authorLu, Yang-Mingen_US
dc.contributor.authorChen, Chi-Liangen_US
dc.contributor.authorLu, Ying-Ruien_US
dc.contributor.authorDong, Chung-Lien_US
dc.contributor.authorHsieh, Ping-Hungen_US
dc.contributor.authorHwang, Weng-Singen_US
dc.contributor.authorChen, Jeng-Lungen_US
dc.contributor.authorChen, Jin-Mingen_US
dc.contributor.authorChan, Ting-Shanen_US
dc.contributor.authorLee, Jyh-Fuen_US
dc.contributor.authorChou, Wu-Chingen_US
dc.date.accessioned2014-12-08T15:35:39Z-
dc.date.available2014-12-08T15:35:39Z-
dc.date.issued2014en_US
dc.identifier.issn1463-9076en_US
dc.identifier.urihttp://hdl.handle.net/11536/24065-
dc.identifier.urihttp://dx.doi.org/10.1039/c3cp54773fen_US
dc.description.abstractVOx films were deposited by radio-frequency reactive magnetron sputtering from a vanadium target at room temperature. Local atomic and electronic structures of the films were then modified by thermal annealing. The oxidation state and structural and gasochromic properties of the films were elucidated by X-ray absorption spectroscopy. Analytical results indicate that the as-deposited VOx films were amorphous with mixed V4+ and V5+ valences. The amorphous VOx had a disordered and expanded lamellar structure resembling that of polymer-intercalated V2O5 gels. VOx films were crystallized into orthorhombic V2O5 at 300 degrees C, and the lamellar structure was eliminated at 400 degrees C. Additionally, the gasochromic reaction reduced the vanadium valence via intervalence transitions between V5+ and V3+. Moreover, removing the lamellar structure reduced the gasochromic rate, and the gasochromic reaction transformed the V2O5 crystalline phase irreversibly into an H1.43V2O5 phase. Based on the results of this study, amorphous VOx with a lamellar structure is recommended for use in H-2 gas sensors.en_US
dc.language.isoen_USen_US
dc.titleLocal geometric and electronic structures of gasochromic VOx filmsen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c3cp54773fen_US
dc.identifier.journalPHYSICAL CHEMISTRY CHEMICAL PHYSICSen_US
dc.citation.volume16en_US
dc.citation.issue10en_US
dc.citation.spage4699en_US
dc.citation.epage4708en_US
dc.contributor.department加速器光源科技與應用學位學程zh_TW
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentMaster and Ph.D. Program for Science and Technology of Accelrrator Light Sourceen_US
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000332393200030-
dc.citation.woscount3-
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