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dc.contributor.authorShu, GWen_US
dc.contributor.authorLee, WZen_US
dc.contributor.authorShu, IJen_US
dc.contributor.authorShen, JLen_US
dc.contributor.authorLin, JCAen_US
dc.contributor.authorChang, WHen_US
dc.contributor.authorRuaan, RCen_US
dc.contributor.authorChou, WCen_US
dc.date.accessioned2014-12-08T15:18:30Z-
dc.date.available2014-12-08T15:18:30Z-
dc.date.issued2005-09-01en_US
dc.identifier.issn1536-125Xen_US
dc.identifier.urihttp://dx.doi.org/10.1109/TNANO.2005.851445en_US
dc.identifier.urihttp://hdl.handle.net/11536/13316-
dc.description.abstractThe effects of oxygen versus vacuum ambients on colloidal CdSe/ZnS quantum dots (QDs) were studied using both continuous and time-resolved photoluminescence (PL) measurements. The PL intensities were found to be an order of magnitude higher in an oxygen atmosphere, which is explained by the passivation of surface defects by oxygen absorption. The decay of PL intensities can be best fitted by a biexponential function with lifetimes of approximately 1 ns; for the fast decay and approximately 10 ns; for the slow decay. Based on the emission-energy dependence of carrier lifetimes and of the amplitude ratio of the fast-decay component to the slow-decay component, we suggest that the fast and slow PL decay of colloidal CdSe/ZnS QDs is caused by the recombination of delocalized carriers in the internal core states and the localized carriers in the surface states, respectively.en_US
dc.language.isoen_USen_US
dc.subjectoptical propertiesen_US
dc.subjectquantum dots (QDs)en_US
dc.titlePhotoluminescence of colloidal CdSe/ZnS quantum dots under oxygen atmosphereen_US
dc.typeArticleen_US
dc.identifier.doi10.1109/TNANO.2005.851445en_US
dc.identifier.journalIEEE TRANSACTIONS ON NANOTECHNOLOGYen_US
dc.citation.volume4en_US
dc.citation.issue5en_US
dc.citation.spage632en_US
dc.citation.epage636en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000231809500022-
dc.citation.woscount25-
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