Self-Hybridized Polaritonic Emission from Layered Perovskites

Light–matter coupling in excitonic materials has been the subject of intense recent investigations due to emergence of new materials. Two-dimensional layered hybrid organic/inorganic perovskites (2D HOIPs) support strongly bound excitons at room temperature with some of the highest oscillator streng...

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Published inNano letters Vol. 21; no. 14; pp. 6245 - 6252
Main Authors Anantharaman, Surendra B, Stevens, Christopher E, Lynch, Jason, Song, Baokun, Hou, Jin, Zhang, Huiqin, Jo, Kiyoung, Kumar, Pawan, Blancon, Jean-Christophe, Mohite, Aditya D, Hendrickson, Joshua R, Jariwala, Deep
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 28.07.2021
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Summary:Light–matter coupling in excitonic materials has been the subject of intense recent investigations due to emergence of new materials. Two-dimensional layered hybrid organic/inorganic perovskites (2D HOIPs) support strongly bound excitons at room temperature with some of the highest oscillator strengths and electric loss tangents among the known excitonic materials. Here, we report strong light–matter coupling in Ruddlesden–Popper phase 2D HOIP crystals without the necessity of an external cavity. We report the concurrent occurrence of multiple orders of hybrid light–matter states via both reflectance and luminescence spectroscopy in thick (>100 nm) crystals and near-unity absorption in thin (<20 nm) crystals. We observe resonances with quality factors of >250 in hybridized exciton-polaritons and identify a linear correlation between exciton-polariton mode splitting and extinction coefficient of the various 2D HOIPs. Our work opens the door to studying polariton dynamics in self-hybridized and open cavity systems with broad applications in optoelectronics and photochemistry.
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USDOE Office of Energy Efficiency and Renewable Energy (EERE)
EE0008843
ISSN:1530-6984
1530-6992
1530-6992
DOI:10.1021/acs.nanolett.1c02058