论文标题
集体振动强耦合下的化学反应性
Chemical reactivity under collective vibrational strong coupling
论文作者
论文摘要
在光腔中进行化学反应的最新实验表现出了改变和引导化学反应的巨大前景,但理论上仍然对其进行了良好的理解。特别是,在集体极限中,腔与某些振动模式之间的共振效应的起源仍需进行积极的研究。在本文中,我们研究了许多分子通过其振动偶极力矩共同与红外腔模式相互作用的单分子解离反应。我们发现,如果腔模式与分子的振动频率共振,反应速率可以通过增加对齐分子的数量来减慢。我们还发现了一个简单的缩放关系,该关系通过集体的Rabi分裂进行缩放,以通过集体振动强耦合来估计反应速率修饰的发作,并在数值上证明了多达10,000个分子的这些效果。
Recent experiments of chemical reactions in optical cavities have shown great promise to alter and steer chemical reactions but still remain poorly understood theoretically. In particular the origin of resonant effects between the cavity and certain vibrational modes in the collective limit is still subject to active research. In this paper, we study unimolecular dissociation reactions of many molecules collectively interacting with an infrared cavity mode through their vibrational dipole moment. We find that the reaction rate can slow down by increasing the number of aligned molecules if the cavity mode is resonant with a vibrational frequency of the molecules. We also discover a simple scaling relation that scales with the collective Rabi splitting to estimate the onset of reaction rate modification by collective vibrational strong coupling and numerically demonstrate these effects for up to 10,000 molecules.