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Dual Strong Couplings Between TPPS J-Aggregates and Aluminum Plasmonic States

机译:TPPS J聚集体与铝等离子体态之间的双重强耦合。

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摘要

We report on the spectral properties of strong coupling between the localized surface plasmon resonances (LSPRs) of aluminum (Al) nanostructures and tetraphenylporphyrin tetrasulfonic acid hydrate (TPPS) J-aggregates. Because of their wide spectral range of LSPR bands from ultraviolet to near-infrared wavelengths by controlling structural size, Al nanodisks can realize strong coupling with different excitons of TPPS J-aggregates. The Rabi splitting energies of the excitons based on Soret and Qbands are 300 and 180 meV, respectively. In addition to extinction spectrum, we have also measured an excitation spectrum to determine the essential absorption of the hybrid states and successfully confirmed a shoulder peak corresponding to a lower branch of hybrid states. In Al nanorod systems, strong coupling with two excitons can also be selectively induced by merely rotating the polarization of the incident light, which constituted a simple platform for the dynamic control of exciton/plasmon coupling states.
机译:我们报告了铝(Al)纳米结构和四苯基卟啉四磺酸水合物(TPPS)J聚集体之间的局部表面等离子体共振(LSPRs)之间的强耦合的光谱性质。通过控制结构尺寸,Al纳米盘具有从紫外线到近红外波长的LSPR波段宽光谱范围,因此可以实现与TPPS J聚集体的不同激子的强耦合。基于Soret和Qband的激子的拉比分裂能分别为300和180 meV。除了消光光谱外,我们还测量了激发光谱以确定杂化态的基本吸收,并成功确认了对应于杂化态下半分支的肩峰。在Al纳米棒系统中,也可以仅通过旋转入射光的偏振来选择性地诱导与两个激子的强耦合,这构成了用于动态控制激子/等离子体激元耦合态的简单平台。

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