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dc.contributor.authorWu, Pin-Jiunen_US
dc.contributor.authorTsuei, Ku-Dingen_US
dc.contributor.authorWei, Kung-Hwaen_US
dc.contributor.authorLiang, Keng S.en_US
dc.date.accessioned2014-12-08T15:15:06Z-
dc.date.available2014-12-08T15:15:06Z-
dc.date.issued2007-01-01en_US
dc.identifier.issn0038-1098en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.ssc.2006.09.048en_US
dc.identifier.urihttp://hdl.handle.net/11536/11344-
dc.description.abstractSize-dependent energy shift of photoemission spectra with respect to bulk sample has been examined for colloidally prepared CdSe nanoparticles with a series of particle sizes. The core-level shifts are well described by a theoretical calculation based on a final-state effect model, whereas an additional initial-state effect due to quantum confinement is required to elucidate the valence-band edge shifts. The results indicate that the interaction between the photohole and the dielectric background in the final state has to be considered in photoemission measurements for organics-passivated nanoparticles. The calculated results in the literature appear to overestimate the initial-state effect compared to our experimental observation. (c) 2006 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectnanostructuresen_US
dc.subjectchemical synthesisen_US
dc.subjectphotoelectron spectroscopiesen_US
dc.subjectsynchrotron radiationen_US
dc.titleEnergy shift of photoemission spectra for organics-passivated CdSe nanoparticles: The final-state effecten_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ssc.2006.09.048en_US
dc.identifier.journalSOLID STATE COMMUNICATIONSen_US
dc.citation.volume141en_US
dc.citation.issue1en_US
dc.citation.spage6en_US
dc.citation.epage11en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000242889000002-
dc.citation.woscount8-
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