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dc.contributor.authorSabatini, Randy P.
dc.contributor.authorZhang, Bolong
dc.contributor.authorGupta, Akhil
dc.contributor.authorLeoni, Julien
dc.contributor.authorWong, Wallace W. H.
dc.contributor.authorLakhwani, Girish
dc.date.accessioned2024-08-26T00:17:43Z
dc.date.available2024-08-26T00:17:43Z
dc.date.issued2019en_AU
dc.identifier.urihttps://hdl.handle.net/2123/32991
dc.description.abstractStrong coupling in organic media holds the promise of efficient room temperature polariton lasing with solution-processed materials. Currently, however, only five pure-organic materials have been shown to demonstrate polariton lasing. A major challenge is to achieve high exciton-photon coupling while maintaining high photoluminescence quantum yield. Here, we utilize a series of diimide perylene materials that possess sterically hindered substituents, dispersed within a polymer matrix. The rigid structures prevent aggregation and allow high photoluminescence quantum yield (PLQY) at large dye loadings. We demonstrate that these systems can exhibit substantial Rabi splittings at dye loadings that yield film PLQYs of up to 85%, making these perylene derivatives promising materials for polariton lasers.en_AU
dc.publisherRoyal Society of Chemistryen_AU
dc.relation.ispartofJournal of Materials Chemistry Cen_AU
dc.rightsCopyright All Rights Reserveden_AU
dc.titleMolecularly isolated perylene diimides enable both strong exciton–photon coupling and high photoluminescence quantum yielden_AU
dc.typeArticleen_AU
dc.identifier.doi10.1039/C9TC00093C
dc.type.pubtypeAuthor accepted manuscripten_AU
dc.relation.arcCE170100026
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume7en_AU
usyd.citation.spage2954en_AU
usyd.citation.epage2960en_AU
workflow.metadata.onlyNoen_AU


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