Polarized Fock States and the Dynamical Casimir Effect in Molecular Cavity Quantum Electrodynamics

被引:57
|
作者
Mandal, Arkajit [1 ]
Vega, Sebastian Montillo [1 ]
Huo, Pengfei [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2020年 / 11卷 / 21期
基金
美国国家科学基金会;
关键词
D O I
10.1021/acs.jpclett.0c02399
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present a new theoretical framework, polarized Fock states (PFSs), to describe the coupled molecule-cavity hybrid system in quantum electrodynamics. Through the quantum light-matter interactions under the dipole Gauge, the molecular permanent dipoles polarize the photon field by displacing the photonic coordinate. Hence, it is convenient to use these shifted Fock states (termed the PFSs) to describe light-matter interactions under the strong coupling regimes. These PFSs are nonorthogonal to each other and are light-matter entangled states. They allow an intuitive understanding of several phenomena that go beyond the prediction of the quantum Rabi model, while also offering numerical convenience to converge the results with much fewer states. With this powerful new theoretical framework, we explain how molecular permanent dipoles lead to the generation of multiple photons from a single electronic excitation (down-conversion), effectively achieving the dynamical Casimir effect through the nuclear vibration instead of cavity mirror oscillations.
引用
收藏
页码:9215 / 9223
页数:9
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