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dc.contributor.authorLin, Yanmingen_US
dc.contributor.authorJiang, Zhenyien_US
dc.contributor.authorZhu, Chaoyuanen_US
dc.contributor.authorHu, Xiaoyunen_US
dc.contributor.authorZhu, Haiyanen_US
dc.contributor.authorZhang, Xiaodongen_US
dc.contributor.authorFan, Junen_US
dc.contributor.authorLin, Sheng Hsienen_US
dc.date.accessioned2014-12-08T15:30:40Z-
dc.date.available2014-12-08T15:30:40Z-
dc.date.issued2013-05-01en_US
dc.identifier.issn0360-3199en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.ijhydene.2013.02.079en_US
dc.identifier.urihttp://hdl.handle.net/11536/21893-
dc.description.abstractThe electronic and optical properties are studied using the density functional theory in (Si,Fe)-codoped anatase TiO2. The calculated results suggest that the synergistic effects of (Si,Fe) codoping can effectively induce the redshift of optical absorption edge, which leads to higher visible-light photocatalytic activity for hydrogen production by water splitting than pure anatase TiO2. To verify the reliability of our calculated results, nanocrystalline (Si,Fe)-codoped TiO2 is synthesized by a sol-gel-solvothermal method, and excellent absorption performance and photocatalytic activity for hydrogen production by water splitting are observed in our experiments. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectTiO2en_US
dc.subjectCodopeden_US
dc.subjectPhotocatalytic activity for hydrogen productionen_US
dc.subjectDensity functional theoryen_US
dc.titleThe optical absorption and hydrogen production by water splitting of (Si,Fe)-codoped anatase TiO2 photocatalysten_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ijhydene.2013.02.079en_US
dc.identifier.journalINTERNATIONAL JOURNAL OF HYDROGEN ENERGYen_US
dc.citation.volume38en_US
dc.citation.issue13en_US
dc.citation.spage5209en_US
dc.citation.epage5214en_US
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000318581000004-
dc.citation.woscount5-
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