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dc.contributor.authorLin, Yan-Chengen_US
dc.contributor.authorChou, Wu-Chingen_US
dc.contributor.authorSusha, Andrei S.en_US
dc.contributor.authorKershaw, Stephen V.en_US
dc.contributor.authorRogach, Andrey L.en_US
dc.date.accessioned2014-12-08T15:30:29Z-
dc.date.available2014-12-08T15:30:29Z-
dc.date.issued2013en_US
dc.identifier.issn2040-3364en_US
dc.identifier.urihttp://hdl.handle.net/11536/21785-
dc.identifier.urihttp://dx.doi.org/10.1039/c3nr33928aen_US
dc.description.abstractThe application of static high pressure provides a method for precisely controlling and investigating many fundamental and unique properties of semiconductor nanocrystals (NCs). This study systematically investigates the high-pressure photoluminescence (PL) and time-resolved carrier dynamics of thiol-capped CdTe NCs of different sizes, at different concentrations, and in various stress environments. The zincblende-to-rocksalt phase transition in thiol-capped CdTe NCs is observed at a pressure far in excess of the bulk phase transition pressure. Additionally, the process of transformation depends strongly on NC size, and the phase transition pressure increases with NC size. These peculiar phenomena are attributed to the distinctive bonding of thiols to the NC surface. In a nonhydrostatic environment, considerable flattening of the PL energy of CdTe NC powder is observed above 3.0 GPa. Furthermore, asymmetric and double-peak PL emissions are obtained from a concentrated solution of CdTe NCs under hydrostatic pressure, implying the feasibility of pressure-induced interparticle coupling.en_US
dc.language.isoen_USen_US
dc.titlePhotoluminescence and time-resolved carrier dynamics in thiol-capped CdTe nanocrystals under high pressureen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c3nr33928aen_US
dc.identifier.journalNANOSCALEen_US
dc.citation.volume5en_US
dc.citation.issue8en_US
dc.citation.spage3400en_US
dc.citation.epage3405en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000316959500040-
dc.citation.woscount0-
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