Microcavity-like exciton-polaritons can be the primary photoexcitation in bare organic semiconductors

Strong-coupling between excitons and confined photonic modes can lead to the formation of new quasi-particles termed exciton-polaritons which can display a range of interesting properties such as super-fluidity, ultrafast transport and Bose-Einstein condensation. Strong-coupling typically occurs whe...

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Hauptverfasser: Pandya, R, Chen, R.Y.S, Gu, Q, Sung, J, Schnedermann, C, Ojambati, O.S, Chikkaraddy, R, Gorman, J, Jacucci, G, Onelli, O.D, Willhammar, T, Johnstone, D.N, Collins, S.M, Midgley, P.A, Auras, F, Baikie, T, Jayaprakash, R, Mathevet, F, Soucek, R, Du, M, Alvertis, A.M, Ashoka, A, Vignolini, S, Lidzey, D.G, Baumberg, J.J, Friend, R.H, Barisien, T, Legrand, L, Chin, A.W, Yuen-Zhou, J, Saikin, S.K, Kukura, P, Musser, A.J, Rao, A
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Sprache:eng
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Zusammenfassung:Strong-coupling between excitons and confined photonic modes can lead to the formation of new quasi-particles termed exciton-polaritons which can display a range of interesting properties such as super-fluidity, ultrafast transport and Bose-Einstein condensation. Strong-coupling typically occurs when an excitonic material is confided in a dielectric or plasmonic microcavity. Here, we show polaritons can form at room temperature in a range of chemically diverse, organic semiconductor thin films, despite the absence of an external cavity. We find evidence of strong light-matter coupling via angle-dependent peak splittings in the reflectivity spectra of the materials and emission from collective polariton states. We additionally show exciton-polaritons are the primary photoexcitation in these organic materials by directly imaging their ultrafast (5 × 106 m s−1), ultralong (~270 nm) transport. These results open-up new fundamental physics and could enable a new generation of organic optoelectronic and light harvesting devices based on cavity-free exciton-polaritons
DOI:10.1038/s41467-021-26617-w