Tahir Zeeshan, Jung Jin-Woo, Rashid Mamoon Ur, Kim Sungdo, Dang Dinh Khoi, Kang Jang-Won, Cho Chang-Hee, Jang Joon I, Kim Yong Soo
Department of Semiconductor Physics and Energy Harvest Storage Research Center, University of Ulsan, Ulsan 44610, South Korea.
Department of Physics and Chemistry, Daegu Gyeongbuk Institute of Science & Technology (DGIST), Daegu 42988, South Korea.
Nanophotonics. 2023 Nov 8;12(23):4297-4306. doi: 10.1515/nanoph-2023-0366. eCollection 2023 Nov.
Controlling coherent light-matter interactions in semiconductor microcavities is at the heart of the next-generation solid-state polaritonic devices. Organic-inorganic hybrid perovskites are potential materials for room-temperature polaritonics owing to their high exciton oscillator strengths and large exciton binding energies. Herein, we report on strong exciton-photon coupling in the micro-platelet and micro-ribbon shaped methylammonium lead bromide single crystals. Owing to high crystallinity and large refractive index, the as-grown perovskite microcrystals serve as self-hybridized optical microcavities along different orientations due to their distinct physical dimensionalities. In this regard, the perovskite micro-platelet forms a simple Fabry-Perot microcavity in out-of-plane orientation, while the micro-ribbon functions as a Fabry-Perot type waveguide microcavity within the plane of the perovskite sample. Consequently, excitons in these microcavities strongly interact with their corresponding uncoupled cavity modes, yielding multimode exciton-polaritons with Rabi splitting energies ∼205 and 235 meV for micro-platelet and micro-ribbon geometry, respectively. Furthermore, micro-ribbon geometry displays Young's double-slit-like interference patterns, which together with the numerical simulation readily reveals the parity and the mode order of the uncoupled cavity modes. Thus, our results not only shed light on strong exciton-photon coupling in various morphologies of methylammonium lead bromide microcrystals but also open an avenue for advanced polaritonic devices.
控制半导体微腔中的相干光与物质相互作用是下一代固态极化激元器件的核心。有机-无机杂化钙钛矿因其高激子振子强度和大激子结合能,是室温极化激元学的潜在材料。在此,我们报道了微片状和微带状甲基溴化铅单晶中的强激子-光子耦合。由于高结晶度和大折射率,生长的钙钛矿微晶因其不同的物理维度,沿不同方向充当自混合光学微腔。在这方面,钙钛矿微片在面外方向形成简单的法布里-珀罗微腔,而微带在钙钛矿样品平面内充当法布里-珀罗型波导微腔。因此,这些微腔中的激子与其相应的未耦合腔模强烈相互作用,对于微片和微带几何结构,分别产生拉比分裂能量约为205和235 meV的多模激子-极化激元。此外,微带几何结构显示出杨氏双缝状干涉图案,这与数值模拟一起很容易揭示未耦合腔模的宇称和模序。因此,我们的结果不仅揭示了甲基溴化铅微晶各种形态中的强激子-光子耦合,还为先进的极化激元器件开辟了一条途径。