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    Dimensionality-dependent energy transfer in polymer-intercalated SnS2 nanocomposites

    P. Parkinson1,*, E. Aharon2, M. H. Chang1, C. Dosche3, G. L. Frey2, A. Köhler3, and L. M. Herz1,†

    • 1Clarendon Laboratory, Parks Road, Oxford OX1 3PU, United Kingdom
    • 2Department of Materials Engineering, Technion-Israel Institute of Technology, Haifa 32000, Israel
    • 3Institute of Physics, University of Potsdam, Am Neuen Palais, Potsdam 14469, Germany

    • *Electronic address: p.parkinson1@physics.ox.ac.uk
    • †Electronic address: l.herz1@physics.ox.ac.uk

    Phys. Rev. B 75, 165206 – Published 30 April, 2007

    DOI: https://doi.org/10.1103/PhysRevB.75.165206

    Abstract

    We have investigated the influence of dimensionality on the excitation-transfer dynamics in a conjugated polymer blend. Using time-resolved photoluminescence spectroscopy, we have measured the transfer transients for both a three-dimensional blend film and for quasi-two-dimensional monolayers formed through intercalation of the polymer blend between the crystal planes of an inorganic SnS2 matrix. We compare the experimental data with a simple, dimensionality-dependent model based on electronic coupling between electronic transition moments taken to be point dipoles. Within this approximation, the energy-transfer dynamics is found to adopt a three-dimensional character in the solid film and a two-dimensional nature in the monolayers present in the SnS2-polymer nanocomposite.

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