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Non-Radiative Energy Transfer in Hybrid Organic-Inorganic Semiconductor Structures<br />
Grigorios Itskos 1 , Colin Belton 2 , Martin D Dawson 3 , Ian M Watson 3 , Ray Murray 2 and Donal D.C. Bradley 2<br />
1 Department of Physics, University of Cyprus, Nicosia, Cyprus<br />
2 Department of Physics, Imperial College London, London, United Kingdom<br />
3 Institute of Photonics, University of Strathclyde, Glasgow, United Kingdom<br />
*g.itskos@imperial.ac.uk<br />
Hybrid organic/inorganic semiconductor structures offer the prospect of new devices that can combine the good electrical<br />
properties of inorganic materials with the attractive luminescence properties of organic materials. Consequently, devices<br />
based on dipole-dipole energy transfer from inorganic semiconductors to conjugated polymers can produce highly efficient<br />
emission across the entire visible spectrum.<br />
We have investigated hybrid structures containing InGaN/GaN single quantum wells (QWs) that are spaced from<br />
fluorene-based polymer films by thin cap layers of GaN. Provided their electronic states are matched [1, 2], the close<br />
proximity of the polymer film to the QW promotes efficient non-radiative (Förster) energy transfer, resulting in a strong<br />
visible emission from the hybrid devices. We have also prepared hybrid structures where white light emission is obtained due<br />
to energy transfer from the InGaN/GaN QW to a blend of polyfluorene emitters.<br />
Temperature-dependent spectrally-resolved measurements show that non-radiative energy transfer from the QW to the<br />
polyfluorene film results in a significant enhancement in the organic emission, with as much as a twenty-fold increase over<br />
that resulting from simple radiative energy transfer [3]. Control measurements (without the QW) verify that the intensity<br />
enhancement is due to energy transfer from the UV-light emitting QW rather than any other effect related to the<br />
polymer/GaN cap layer interface. Time-resolved experiments show a significant reduction in the QW decay time providing<br />
further insight into the non-radiative nature of the transfer [4]. In addition, we have verified that non-radiative energy transfer<br />
also occurs from the inorganic well to thin layers of carefully adjusted polymer blends in which cascade non-radiative energy<br />
transfer results in the emission of white light.<br />
[1] D. Basko, G.C. La Rocca, F. Bassani and V.M. Agranovich, Eur. Phys. J. B 8, 353, (1999)<br />
[2] Š. Kos, M. Achermann, V.I. Klimov and D.L. Smith, Phys. Rev. B, 71, 205309, (2005)<br />
[3] G. Heliotis, G. Itskos, R. Murray, M.D. Dawson, I.M. Watson and D.D.C. Bradley, Adv. Materials 18, 334, (2006)<br />
[4] G. Itskos, G. Heliotis, P. G. Lagoudakis, J. Lupton, N.P. Barradas, E. Alves, S. Pereira, I. M. Watson, M. D. Dawson, J.<br />
Feldmann, R. Murray and D. D. C. Bradley, accepted in Phys. Rev. B<br />
4