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自组装分子与表面等离激元极化激元之间的强耦合

Strong Coupling between Self-Assembled Molecules and Surface Plasmon Polaritons.

作者信息

Bigeon J, Le Liepvre S, Vassant S, Belabas N, Bardou N, Minot C, Yacomotti A, Levenson A, Charra F, Barbay S

机构信息

Centre de Nanosciences et de Nanotechnologies, CNRS, Université Paris-Sud, Université Paris-Saclay , C2N Marcoussis, 91460 Marcoussis, France.

Service de Physique de l' État Condensé, SPEC-CEA, CNRS, Université Paris-Saclay, CEA Saclay , F-91191 Gif-sur-Yvette, France.

出版信息

J Phys Chem Lett. 2017 Nov 16;8(22):5626-5632. doi: 10.1021/acs.jpclett.7b02586. Epub 2017 Nov 7.

DOI:10.1021/acs.jpclett.7b02586
PMID:29094949
Abstract

We experimentally demonstrate strong coupling between self-assembled PTCDI-C7 organic molecules and the electromagnetic mode generated by surface plasmon polaritons (SPPs). The system consists of a dense self-assembly of ordered molecules evaporated directly on a thin gold film, which stack perpendicularly to the metal surface to form H-aggregates, without a host matrix. Experimental wavevector-resolved reflectance spectra show the formation of hybrid states that display a clear anticrossing, attesting the strong coupling regime with a Rabi splitting energy of Ω ≃ 102 meV at room temperature. We demonstrate that the strength of the observed strong coupling regime derives from the high degree of organization of the dense layers of self-assembled molecules at the nanoscale that results in the concentration of the oscillator strength in a charge-transfer Frenkel exciton, with a dipole moment parallel to the direction of the maximum electric field. We compare our results to numerical simulations of a transfer matrix model and reach good qualitative agreement with the experimental findings. In our nanophotonic system, the use of self-assembled molecules opens interesting prospects in the context of strong coupling regimes with molecular systems.

摘要

我们通过实验证明了自组装的PTCDI-C7有机分子与表面等离激元极化激元(SPP)产生的电磁模式之间的强耦合。该系统由直接蒸发在薄金膜上的有序分子的致密自组装组成,这些分子垂直于金属表面堆叠形成H聚集体,无需主体基质。实验性的波矢分辨反射光谱显示形成了具有明显反交叉的混合态,证明了在室温下拉比分裂能量为Ω≃102 meV的强耦合区域。我们证明,观察到的强耦合区域的强度源于纳米尺度上自组装分子致密层的高度组织性,这导致振子强度集中在电荷转移弗伦克尔激子中,其偶极矩平行于最大电场方向。我们将结果与转移矩阵模型的数值模拟进行比较,与实验结果达成了良好的定性一致。在我们的纳米光子系统中,自组装分子的使用在与分子系统的强耦合区域背景下开辟了有趣的前景。

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