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dc.contributor.authorYuan, C. T.en_US
dc.contributor.authorChou, W. C.en_US
dc.contributor.authorTang, J.en_US
dc.contributor.authorLin, C. A.en_US
dc.contributor.authorChang, W. H.en_US
dc.contributor.authorShen, J. L.en_US
dc.contributor.authorChuu, D. S.en_US
dc.date.accessioned2019-04-03T06:42:19Z-
dc.date.available2019-04-03T06:42:19Z-
dc.date.issued2009-08-31en_US
dc.identifier.issn1094-4087en_US
dc.identifier.urihttp://dx.doi.org/10.1364/OE.17.016111en_US
dc.identifier.urihttp://hdl.handle.net/11536/6782-
dc.description.abstractBoth ensemble and single-molecule measurements were performed to explore the fluorescence properties of Au nanoclusters (NCs). Photoinduced fluorescence enhancement was observed for ensemble NCs in solution, but photobleaching was found at ambient environments. At the single-molecule level, fluorescence blinking and single-step photobleaching were observed. Furthermore, their time-resolved fluorescence shows a single exponential decay with a lifetime of similar to 7 ns and is insensitive to changes in fluorescence intensity. The lifetime distribution is more homogeneous within ensemble Au NCs as compared to CdSe QDs. Therefore, Au NCs have potential applications as nontoxic fluorescent labels for lifetime-based imaging microscopy. However, their low quantum yields and poor photostability are disadvantageous factors, which require further improvement. (C) 2009 Optical Society of Americaen_US
dc.language.isoen_USen_US
dc.titleSingle fluorescent gold nanoclustersen_US
dc.typeArticleen_US
dc.identifier.doi10.1364/OE.17.016111en_US
dc.identifier.journalOPTICS EXPRESSen_US
dc.citation.volume17en_US
dc.citation.issue18en_US
dc.citation.spage16111en_US
dc.citation.epage16118en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000269781700075en_US
dc.citation.woscount21en_US
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