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dc.contributor.authorChen, Jiaen_US
dc.contributor.authorJia, Shuoxunen_US
dc.contributor.authorJi, Xiaohuanen_US
dc.contributor.authorNourrein, Mohameden_US
dc.contributor.authorXiang, Hengxueen_US
dc.contributor.authorZhou, Zheen_US
dc.contributor.authorWang, Chien-Lungen_US
dc.contributor.authorSun, Binen_US
dc.contributor.authorZhu, Meifangen_US
dc.date.accessioned2019-04-02T05:59:48Z-
dc.date.available2019-04-02T05:59:48Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c8ra04158jen_US
dc.identifier.urihttp://hdl.handle.net/11536/148364-
dc.description.abstractAggregation and continuous -stacking have been the major obstacles hindering the fluorescence (FL) quantum yield (phi(F)) of perylene diimide (PDI) derivatives in the condensed phase. To prepare polymer microspheres with nearly unity phi(F), in this work a POSS functionalized PDI derivative, POSS-PDI-POSS (PPP), was applied as the red fluorophore of poly(3-hydroxylbutyrate-co-3-hydroxyvalerate) (PHBV) and polystyrene (PS) microspheres. The electrosprayed PPP/PHBV and PPP/PS microspheres have unique hollow structures. Moreover, they show bright red FL under a fluorescence microscope. A photophysical study of the microspheres indicates a significant role of the polymer matrix in disrupting the aggregation state and the phi(F) of the embedded PPP fluorophore. Both the PPP/PHBV and the PPP/PS microspheres show higher phi(F) than most PDI materials in the condensed phase. The PPP/PHBV microspheres show phi(F) of 28%, whereas the PPP/PS microspheres give nearly unity phi(F).en_US
dc.language.isoen_USen_US
dc.titleThe morphologies and fluorescence quantum yields of perylene diimide dye-doped PS and PHVB microspheresen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c8ra04158jen_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.volume8en_US
dc.citation.spage35534en_US
dc.citation.epage35538en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000448348900024en_US
dc.citation.woscount0en_US
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