Yu Qi, Zhang Dong H, Bowman Joel M
Department of Chemistry, Fudan University, Shanghai, China.
Shanghai Innovation Institute, Shanghai, China.
Nat Commun. 2025 Jul 22;16(1):6760. doi: 10.1038/s41467-025-62117-x.
Recent experiments have demonstrated that vibrational strong coupling (VSC) between molecular vibrations and the optical cavity field can modify vibrational energy transfer (VET) processes in molecular systems. However, the underlying mechanisms and the behavior of individual molecules under collective VSC remain largely incomplete. In this work, we combine state-of-the-art quantum vibrational spectral calculation, quantum wavepacket dynamics simulations, and ab initio machine-learning potential to elucidate how the vibrational dynamics of water OH stretches can be altered by VSC. Taking the -cavity system as an example, we show that the collective VSC breaks the localization picture, promotes the delocalization of OH stretches, and opens new intermolecular vibrational energy pathways involving both neighboring and remote water molecules. The manipulation of the VET process relies on the alignment of the transition dipole moment orientations of the corresponding vibrational states. The emergence of new energy transfer pathways is found to be attributed to cavity-induced vibrational resonance involving OH stretches across different water molecules, along with alterations in mode coupling patterns.
最近的实验表明,分子振动与光学腔场之间的振动强耦合(VSC)可以改变分子系统中的振动能量转移(VET)过程。然而,集体VSC下的潜在机制以及单个分子的行为在很大程度上仍不完整。在这项工作中,我们结合了最先进的量子振动光谱计算、量子波包动力学模拟和从头算机器学习势,以阐明VSC如何改变水的OH伸缩振动动力学。以 - 腔系统为例,我们表明集体VSC打破了局域化图景,促进了OH伸缩的离域化,并开辟了涉及相邻和远程水分子的新的分子间振动能量途径。VET过程的操纵依赖于相应振动状态的跃迁偶极矩取向的排列。发现新的能量转移途径的出现归因于涉及不同水分子间OH伸缩的腔诱导振动共振以及模式耦合模式的改变。