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Triplet exciton transport in isotopic mixed naphthalene crystals. I. Kinetic analysis of trapping and fusion
dc.contributor.authorGentry, Stuart T.en_US
dc.contributor.authorKopelman, Raoulen_US
dc.date.accessioned2010-05-06T22:09:37Z
dc.date.available2010-05-06T22:09:37Z
dc.date.issued1984-10-01en_US
dc.identifier.citationGentry, Stuart T.; Kopelman, R. (1984). "Triplet exciton transport in isotopic mixed naphthalene crystals. I. Kinetic analysis of trapping and fusion." The Journal of Chemical Physics 81(7): 3014-3021. <http://hdl.handle.net/2027.42/70437>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/70437
dc.description.abstractTime‐resolved triplet exciton transport in binary mixed crystals has been studied for C10H8 in C10D8 (20%–100%) at liquid helium temperatures. The delayed fluorescence decays are exponential and range from milliseconds to nanoseconds as Cg goes from 0.2 to 1.0. The analysis is based on the presence of a BMN supertrap in large amounts (10−3) and on the fact that supertrapping of the guest excitons dominates the kinetics while heterofusion (triplet guest‐triplet supertrap annihilation) dominates over the homofusion (guest–guest annihilation) and was used to monitor the kinetics. We also investigated in detail photodetrapping and the relative efficiencies of the various fusion channels. An analysis of the transport data is given in paper II.en_US
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dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleTriplet exciton transport in isotopic mixed naphthalene crystals. I. Kinetic analysis of trapping and fusionen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, Ann Arbor, Michigan 48109en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/70437/2/JCPSA6-81-7-3014-1.pdf
dc.identifier.doi10.1063/1.448054en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
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dc.owningcollnamePhysics, Department of


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