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dc.contributor.authorChen, CYen_US
dc.contributor.authorCheng, CTen_US
dc.contributor.authorYu, JKen_US
dc.contributor.authorPu, SCen_US
dc.contributor.authorCheng, YMen_US
dc.contributor.authorChou, PTen_US
dc.contributor.authorChou, YHen_US
dc.contributor.authorChiu, HTen_US
dc.date.accessioned2014-12-08T15:38:47Z-
dc.date.available2014-12-08T15:38:47Z-
dc.date.issued2004-07-29en_US
dc.identifier.issn1520-6106en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jp049177wen_US
dc.identifier.urihttp://hdl.handle.net/11536/26556-
dc.description.abstractCdSe/ZnTe type-II quantum dots (QDs) synthesized via the CdO precursor are reported. Spectroscopic and femtosecond dynamic measurements reveal that the rate of photoinduced electron/hole spatial separation decreases with increases in the size of the core, and it is independent of the thickness of the shell in the CdSe/ZnTe QDs. The results are consistent with the binding strength of the electron and hole confined at the center of CdSe. The correlation between the core/shell size and the electron/hole spatial separation rate resolved in this study may provide valuable information for applications where rapid photoinduced carrier separation followed by charge transfer into a matrix or electrode is crucial, such as in photovoltaic devices.en_US
dc.language.isoen_USen_US
dc.titleSpectroscopy and femtosecond dynamics of type-II CdSe/ZnTe core-shell semiconductor synthesized via the CdO precursoren_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jp049177wen_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Ben_US
dc.citation.volume108en_US
dc.citation.issue30en_US
dc.citation.spage10687en_US
dc.citation.epage10691en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000222864200014-
dc.citation.woscount70-
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