Aleesha George, River B. Carson, Daniel J. Gracias, Thomas J. Ugras, Richard D. Robinson* and Andrew J. Musser*,
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引用次数: 0
摘要
强光-物质耦合形成极化子在材料工程、光电子学等领域的应用受到了广泛的关注。它们的基础状态的组合特性允许许多优点,如长距离的离域,室温玻色-爱因斯坦凝聚和能量状态的可调性。然而,很少有激子-极化系统能够进入紫外线,并且确定具有大振荡器强度,大激子结合能,易于加工并且对器件集成稳定的理想材料已被证明具有挑战性。在这里,我们证明了cd魔术大小集群(MSCs)结合了所有这些特征。在金属Fabry-Perot (FP)腔中进行简单的溶液处理可以使MSCs表现出室温强耦合,正如Rabi分裂对发色团浓度的平方根依赖性所证明的那样。可以实现390 meV的拉比分裂,极化态发射范围从3.07 eV (403 nm)到3.64 eV (340 nm)。当拉比分裂通过激子线宽度归一化时,该系统可与可见光范围内的高性能系统相媲美,并超过了已报道的紫外极化系统。这些间充质干细胞的强紫外吸收为开发具有近紫外可调性的稳定极化器件奠定了基础。
Near-UV Tunable Polaritons from Magic-Size Clusters
Stronglight-matter coupling to form polaritons has gained significant attention for its applications in materials engineering, optoelectronics, and beyond. The combined properties of their underlying states allow for numerous advantages such as delocalization over long distances, room-temperature Bose–Einstein condensation, and tunability of energy states. Few exciton-polariton systems, however, reach into the UV, and identifying ideal materials that possess large oscillator strengths, large exciton binding energies, ease of processing, and that are stable for device integration has proven challenging. Here, we demonstrate that CdS magic-size clusters (MSCs) combine all these traits. Simple solution processing in metallic Fabry–Perot (FP) cavities enables the MSCs to exhibit room-temperature strong coupling, as demonstrated by the square root dependence of Rabi splitting on chromophore concentration. Rabi splitting as large as 390 meV can be achieved, with emission from polariton states spanning from 3.07 eV (403 nm) to 3.64 eV (340 nm). When Rabi splittings are normalized by the excitonic line width, this system is comparable with high-performing systems in the visible range and surpasses reported UV polariton systems. The strong UV absorption of these MSCs establishes a platform to develop stable polaritonic devices with tunability across the near-UV.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.