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Charge-transfer excitons in strongly coupled organic semiconductors

dc.contributor.authorGlowe, J. -Fen
dc.contributor.authorPerrin, M.en
dc.contributor.authorBeljonne, D.en
dc.contributor.authorHayes, Sophia C.en
dc.contributor.authorGardebien, F.en
dc.contributor.authorSilva, C.en
dc.creatorGlowe, J. -Fen
dc.creatorPerrin, M.en
dc.creatorBeljonne, D.en
dc.creatorHayes, Sophia C.en
dc.creatorGardebien, F.en
dc.creatorSilva, C.en
dc.date.accessioned2019-11-21T06:19:11Z
dc.date.available2019-11-21T06:19:11Z
dc.date.issued2010
dc.identifier.issn1098-0121
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55513
dc.description.abstractTime-resolved and temperature-dependent photoluminescence measurements on one-dimensional sexithiophene lattices reveal intrinsic branching of photoexcitations to two distinct species: self-trapped excitons and dark charge-transfer excitons (CTXsen
dc.description.abstract5% yield), with radii spanning 2-3 sites. The significant charge-transfer exciton (CTX) yield results from the strong charge-transfer character of the Frenkel exciton band due to the large free-exciton bandwidth (∼400meV) in these supramolecular nanostructures. © 2010 The American Physical Society.en
dc.sourcePhysical Review B - Condensed Matter and Materials Physicsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-77954823588&doi=10.1103%2fPhysRevB.81.041201&partnerID=40&md5=b6877426b1d9179e6ca7dcb5eaaafebb
dc.titleCharge-transfer excitons in strongly coupled organic semiconductorsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1103/PhysRevB.81.041201
dc.description.volume81
dc.description.issue4
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :5</p>en
dc.source.abbreviationPhys.Rev.B Condens.Matter Mater.Phys.en
dc.contributor.orcidHayes, Sophia C. [0000-0002-2809-6193]
dc.gnosis.orcid0000-0002-2809-6193


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