论文标题

在手性吸附的单分子中的Trion-Libron耦合的证据

Evidence of trion-libron coupling in chirally adsorbed single molecules

论文作者

Doležal, Jiří, Canola, Sofia, Hapala, Prokop, Ferreira, Rodrigo Cezar de Campos, Merino, Pablo, Švec, Martin

论文摘要

分子中核和激发电子的运动之间的相互作用在生物学和人工纳米机器中都起着关键作用。在这里,我们提供了量化的库模式(库)(库)之间的耦合以及在表面上吸附的单个邻苯烷酰胺染料上的激发态(TRIONS)之间的耦合。通过隧穿电子诱导的电致发光,我们在手感吸附的邻苯二甲胺的光谱中鉴定出在μEV能量范围内的库中,否则它们是从对称吸附的物种的光谱中不存在的。实验测量的库光谱很好地匹配了理论上计算的库元特征力和峰值强度(弗兰克 - 康登因子),并揭示了激发态的零库子的意外人口减少通道,可以通过调谐纳米腔的大小来有效地控制,纳米腔的大小可以有效地控制。我们的结果展示了使用μEV分辨尖端增强光谱法通过其低能分子模式来表征分子动力学的可能性。

Interplay between motion of nuclei and excited electrons in molecules plays a key role both in biological and artificial nanomachines. Here we provide a detailed analysis of coupling between quantized librational modes (librons) and charged excited states (trions) on single phthalocyanine dyes adsorbed on a surface. By means of tunnelling electron-induced electroluminescence, we identify libronic progressions on a μeV energy range in spectra of chirally adsorbed phthalocyanines, which are otherwise absent from spectra of symmetrically adsorbed species. Experimentally measured libronic spectra match very well the theoretically calculated libron eigenenergies and peak intensities (Franck-Condon factors) and reveal an unexpected depopulation channel for the zero libron of the excited state that can be effectively controlled by tuning the size of the nanocavity. Our results showcase the possibility of characterizing the dynamics of molecules by their low-energy molecular modes using μeV-resolved tip-enhanced spectroscopy.

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