School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences and Tel Aviv University Center for Light-Matter Interaction, Tel Aviv University, Tel Aviv, 6997801, Israel.
Nat Commun. 2019 Jul 19;10(1):3248. doi: 10.1038/s41467-019-11130-y.
Several years ago, strong coupling between electronic molecular transitions and photonic structures was shown to modify the electronic landscape of the molecules and affect their chemical behavior. Since then, this concept has evolved into a new field known as polaritonic chemistry. An important ingredient in the progress of this field was the demonstration of strong coupling with intra-molecular vibrations, which enabled the modification of processes occurring at the electronic ground-state. Here we demonstrate strong coupling with collective, inter-molecular vibrations occurring in organic materials in the low-terahertz region ([Formula: see text]10 Hz). Using a cavity filled with α-lactose molecules, we measure the temporal evolution and observe coherent Rabi oscillations, corresponding to a splitting of 68 GHz. These results take strong coupling into a new class of materials and processes, including skeletal polymer motions, protein dynamics, metal organic frameworks and other materials, in which collective, spatially extended degrees of freedom participate in the dynamics.
几年前,电子分子跃迁与光子结构之间的强耦合被证明可以改变分子的电子结构,并影响它们的化学行为。从那时起,这一概念发展成为一个新的领域,即极化激元化学。这一领域的进展的一个重要因素是展示了与分子内振动的强耦合,这使得可以对电子基态发生的过程进行修饰。在这里,我们证明了在低太赫兹区([Formula: see text]10 Hz)的有机材料中发生的集体分子间振动的强耦合。我们使用充满α-乳糖分子的腔来测量时间演化并观察到相干拉比振荡,这对应于 68 GHz 的分裂。这些结果将强耦合带入了一个新的材料和过程类别,包括骨架聚合物运动、蛋白质动力学、金属有机骨架和其他材料,其中集体的、空间扩展的自由度参与动力学。