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Correlated hopping model for singlet exciton transport in lightly dohttp://www.sciencedirect.com/science/article/B6TFM-44DTGD2-KF/2/d498b4c6ab57aaaa33fd7a30ddc18badped naphthalene crystals

dc.contributor.authorArgyrakis, Panosen_US
dc.contributor.authorKopelman, Raoulen_US
dc.date.accessioned2006-04-07T17:21:39Z
dc.date.available2006-04-07T17:21:39Z
dc.date.issued1980-09-15en_US
dc.identifier.citationArgyrakis, Panos, Kopelman, Raoul (1980/09/15)."Correlated hopping model for singlet exciton transport in lightly doped naphthalene crystals." Chemical Physics 51(1-2): 9-16. <http://hdl.handle.net/2027.42/23147>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TFM-44DTGD2-KF/2/d498b4c6ab57aaaa33fd7a30ddc18baden_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23147
dc.description.abstractA formalism of correlated lattice random walk is applied to the singlet exciton transport in naphthalene. Fluorescence experiments on excitation migration in naphthalene crystals (C10H8 and C10D8), lightly doped chemically (anthracene) or isotopically (C10DH7), over a wide temperature range (2-300 K) are interpreted in terms of a correlated hopping model. The hopping time is found to be of the order of 1 ps. The increase in the overall quenching (supertrapping) efficiency with reduced temperature is interpreted in terms of an increase by one or more orders of magnitude in the parameter of coherency (hopping correlation). The role of the trapping cross section is discussed.en_US
dc.format.extent708580 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleCorrelated hopping model for singlet exciton transport in lightly dohttp://www.sciencedirect.com/science/article/B6TFM-44DTGD2-KF/2/d498b4c6ab57aaaa33fd7a30ddc18badped naphthalene crystalsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbsecondlevelMathematicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23147/1/0000071.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0301-0104(80)80075-9en_US
dc.identifier.sourceChemical Physicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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