Theoretische Chemie, Physikalisch-Chemisches Institut, Universität Heidelberg, INF 229, D-69120 Heidelberg, Germany.
J Phys Chem A. 2023 Feb 23;127(7):1598-1608. doi: 10.1021/acs.jpca.2c08608. Epub 2023 Feb 9.
Intramolecular vibrational energy redistribution (IVR) plays a significant role in cavity-modified chemical reaction rates. As such, understanding the fundamental mechanisms by which the cavity modifies the IVR pathways is a fundamental step toward engineering the effect of the confined electromagnetic modes on the outcome of chemical processes. Here we consider an ensemble of two-mode molecules with intramolecular anharmonic couplings interacting with an infrared cavity mode and consider their quantum dynamics and infrared spectra. Polaritonic Fermi resonances involving fundamental and overtone states of the polaritonic subsystem mediate efficient energy transfer pathways between otherwise off-resonant molecular states. These pathways are of collective nature, yet enabled by the intramolecular anharmonic couplings. Hence, through polaritonic Fermi resonances, cavity excitation can efficiently spread toward low-frequency modes while becoming delocalized over several molecules.
分子内振动能量转移(IVR)在腔修饰化学反应速率中起着重要作用。因此,理解腔如何改变 IVR 途径的基本机制是工程化受限电磁场模式对化学过程结果的影响的基本步骤。在这里,我们考虑了一组与红外腔模式相互作用的具有分子内非谐耦合的双模分子,并考虑了它们的量子动力学和红外光谱。涉及极化子子系统基态和泛频态的极化子费米共振为原本非共振的分子态之间提供了有效的能量转移途径。这些途径具有集体性质,但得益于分子内非谐耦合。因此,通过极化子费米共振,腔激发可以有效地向低频模式传播,同时在几个分子之间扩散。