We report the observation of strong coupling between exciton and photon modes in a conjugated polymer-based semiconductor microcavity. Thin films of the σ-conjugated poly[bis(p-butylphenyl)silane] (PBPS) were inserted between metal and dielectric mirrors to form the microcavity structures. Variation of the PBPS film thickness between 80 and 140 nm allowed the cavity photon resonance to be tuned in the vicinity of the free exciton energy. The expected anticrossing behavior, with intensity and linewidth averaging, was observed at room temperature in the cavity reflection spectra and the vacuum Rabi splitting was found to be This large value is consistent with the expectations of transfer matrix reflectivity calculations performed with optical constants data derived from a Kramers–Kronig analysis of the PBPS absorption spectrum. Angle-dependent photoluminescence measurements were performed for the microcavity with a 120 nm thickness PBPS layer. Unlike the emission from a standard, weakly coupled, cavity, the polariton emission shows almost no blueshift with angle, a desirable feature for potential display applications.
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24 March 2003
Research Article|
March 24 2003
Polariton emission from polysilane-based organic microcavities
Noriyuki Takada;
Noriyuki Takada
Photonics Research Institute, National Institute of Advanced Industrial Science and Technology, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan
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Toshihide Kamata;
Toshihide Kamata
Photonics Research Institute, National Institute of Advanced Industrial Science and Technology, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan
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Donal D. C. Bradley
Donal D. C. Bradley
Department of Physics, Imperial College London, Prince Consort Road, London SW7 2BW, United Kingdom
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Appl. Phys. Lett. 82, 1812–1814 (2003)
Article history
Received:
October 21 2002
Accepted:
January 22 2003
Citation
Noriyuki Takada, Toshihide Kamata, Donal D. C. Bradley; Polariton emission from polysilane-based organic microcavities. Appl. Phys. Lett. 24 March 2003; 82 (12): 1812–1814. https://doi.org/10.1063/1.1559950
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