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Understanding the polaritonic ground state in cavity quantum electrodynamics
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Molecular polaritons arise when molecules interact so strongly with light that they become entangled with each other. This light-matter hybridization alters the chemical and physical properties of the molecular system and allows chemical reactions to be controlled without the use of external fields. We investigate the impact of strong light-matter coupling on the electronic structure using perturbative approaches and demonstrate that Rayleigh-Schr\"odinger perturbation theory can reproduce the ground state energies in optical cavities to comparable accuracy as ab initio cavity quantum electrodynamics methodologies for currently relevant coupling strengths. The method is effective in both low and high cavity frequency regimes and straightforward to implement via response functions. Furthermore, we establish simple relations between cavity-induced intermolecular forces and van der Waals forces. These findings provide valuable insight into the manipulation of ground-state polaritonic energy landscapes, shedding light on the systems and conditions in which modifications can be achieved.
Forward citations
Cited by 2 Pith papers
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Static Electric Dipole Polarizability and Hyperpolarizability Tensors from Mean-Field Cavity Quantum Electrodynamics Approaches
Static QED-HF/QED-DFT response theory shows the first hyperpolarizability of p-nitroaniline drops by more than 20% at lambda=0.05 a.u. in a z-polarized cavity, while the polarizability changes by only a few percent.
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Auxiliary Field Quantum Monte Carlo for Electron-Photon Correlation
QED-AFQMC matches full configuration interaction for the polaritonic ground state of HF and predicts cavity-modified isomerization barriers for C2N2H6.
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