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Exciton percolation I. Migration dynamics

dc.contributor.authorHoshen, Josephen_US
dc.contributor.authorKopelman, Raoulen_US
dc.date.accessioned2010-05-06T23:19:33Z
dc.date.available2010-05-06T23:19:33Z
dc.date.issued1976-10-01en_US
dc.identifier.citationHoshen, Joseph; Kopelman, Raoul (1976). "Exciton percolation I. Migration dynamics." The Journal of Chemical Physics 65(7): 2817-2823. <http://hdl.handle.net/2027.42/71176>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/71176
dc.description.abstractThe exciton transfer, via migration and trapping, in binary and ternary mixed crystals is formulated in terms of percolation theory and the cluster structure for binary randomly mixed crystals. An important limiting case (exciton supertransfer) is derived for long exciton lifetime, relative to jumping and trapping time. The exciton supertransfer case is solved analytically [in terms of the functions derived by J. Hoshen and R. Kopelman, Phys. Rev. B (in press)] and the solutions involve neither physical parameters nor physical constants. Other limiting cases are derived, as well as an algorithm for the general energy transfer case. This algorithm relates the migration and trapping in binary and ternary systems with the trapping‐free migration in binary systems. The algorithm involves the use of empirical information, i.e., the parameters describing the exciton dynamics in a pure crystal. The various formulations are valid for concentrations both above and below the critical (’’percolation’’) concentration, with due emphasis on small, medium, and large cluster contributions. Sample calculations are given (for the square lattice with site percolation).en_US
dc.format.extent3102 bytes
dc.format.extent469286 bytes
dc.format.mimetypetext/plain
dc.format.mimetypeapplication/pdf
dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleExciton percolation I. Migration dynamicsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/71176/2/JCPSA6-65-7-2817-1.pdf
dc.identifier.doi10.1063/1.433430en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
dc.identifier.citedreferenceJ. Hoshen and R. Kopelman, Phys. Rev. B (in press).en_US
dc.identifier.citedreferenceV. K. S. Shante and S. Kirkpatrick, Adv. Phys. 20, 325 (1971).en_US
dc.identifier.citedreferenceS. Kirkpatrick, Rev. Mod. Phys. 45, 574 (1973).en_US
dc.identifier.citedreferenceR. Kopelman, Excitons in Pure and Mixed Molecular Crystals, Excited States (Academic, New York, 1975) Vol. II.en_US
dc.identifier.citedreferenceR. Kopelman, E. M. Monberg, F. W. Ochs, and P. N. Prasad, Phys. Rev. Lett. 34, 1506 (1975).en_US
dc.identifier.citedreferenceR. Kopelman, E. M. Monberg, F. W. Ochs, and P. N. Prasad, J. Chem. Phys. 62, 292 (1975).en_US
dc.identifier.citedreferenceF. W. Ochs, Ph.D. Thesis, Univ. of Michigan (1974); F. W. Ochs and R. Kopelman, (unpublished).en_US
dc.identifier.citedreferenceR. Kopelman, J. Lumin. 12, 775 (1976); J. Phys. Chem. (in press).en_US
dc.identifier.citedreferenceH.‐K. Hong and R. Kopelman, J. Chem. Phys. 55, 5380 (1971).en_US
dc.identifier.citedreferenceJ. Hoshen, E. M. Monberg, and R. Kopelman (unpublished).en_US
dc.identifier.citedreferenceE. M. Monberg and R. Kopelman (unpublished).en_US
dc.identifier.citedreferenceP. Argyrakis and R. Kopelman (unpublished).en_US
dc.identifier.citedreferenceSee, for instance, J. Koo, L. R. Walter, and G. Geschwind, Phys. Rev. Lett. 35, 1669 (1975). However, in this particular experimental situation we wonder to what extent the thermal activation and deactivation require explicit recognition.en_US
dc.identifier.citedreferenceP. W. Anderson, Phys. Rev. 109, 1492 (1958).en_US
dc.owningcollnamePhysics, Department of


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