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dc.contributor.authorYang, CCen_US
dc.contributor.authorCheng, SYen_US
dc.contributor.authorLee, HYen_US
dc.contributor.authorChen, SYen_US
dc.date.accessioned2014-12-08T15:17:40Z-
dc.date.available2014-12-08T15:17:40Z-
dc.date.issued2006en_US
dc.identifier.issn0272-8842en_US
dc.identifier.urihttp://hdl.handle.net/11536/12821-
dc.identifier.urihttp://dx.doi.org/10.1016/j.ceramint.2004.11.016en_US
dc.description.abstractEuropium doped zinc oxide (Eu:ZnO) powder has been prepared by mixing ZnO and Eu2O3 in deionized water and acetone solvents. The influence of phase transformation of Eu-doped ZnO powders mixed in different solvents on the luminescence behavior has been investigated. When the powder was mixed in deionized water and then sintered at high temperatures, Eu3+ ions were detected in the ZnO matrix. The intrinsic red photoluminescence (D-5(0)->F-7(2)) of Eu3+ was easily shielded by the ZnO intrinsic defect as the samples were excited with 325 nm short wavelength as a consequence of the energy level of Eu-Zn(circle) (0.19 eV) being closer to conduction band than the one of Zn-1(circle circle) (0.22 eV). Therefore, no red emission can be detected. In contrast, as the Eu-doped ZnO powder was mixed in acetone solvent (without OH-), no Eu3+ ions could be detected in the ZnO matrix. In addition, the red emission could be detected not only under excitation with long wavelength (532 nm) but also at short wavelength (325 nm). (C) 2005 Elsevier Ltd and Techna Group S.r.l. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectmixingsen_US
dc.subjectoptical propertiesen_US
dc.subjectZnOen_US
dc.subjectEu2O3en_US
dc.titleEffects of phase transformation on photoluminescence behavior of ZnO : Eu prepared in different solventsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ceramint.2004.11.016en_US
dc.identifier.journalCERAMICS INTERNATIONALen_US
dc.citation.volume32en_US
dc.citation.issue1en_US
dc.citation.spage37en_US
dc.citation.epage41en_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:000234243700006-
dc.citation.woscount35-
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