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Observations of intermolecular excimers in several pi-conjugated polymers and exciplexes of these polymers with tris(p-tolyl) amine are reported. It is shown that the luminescence of conjugated polymer thin films originates from excimer emission and that the generally low quantum yield is the result of self-quenching. Thus, in sufficiently dilute solution, the "single-chain" emission has a quantum yield of unity. Exciplex luminescence and exciplex-mediated charge photogeneration have much higher quantum yields than the excimer-mediated photophysical processes. These results provide a basis for understanding and controlling the photophysics of conjugated polymers in terms of supramolecular structure and morphology.
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Samson A. Jenekhe
University of Akron
John A. Osaheni
General Electric (United States)
Science
University of Rochester
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Jenekhe et al. (Fri,) studied this question.
synapsesocial.com/papers/6a0654e8d05e6a3d0b0fe4cb — DOI: https://doi.org/10.1126/science.265.5173.765
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