The coherent-state transformation in quantum electrodynamics coupled cluster theory

TL;DR

This paper investigates the coherent-state transformation in quantum electrodynamics coupled cluster theory, revealing how it affects the correlation energy and ground state, especially in low-frequency regimes and charged systems.

Contribution

It introduces a novel CS-based approach to QED-CC, differing from previous methods by using photon-added coherent states and analyzing its impact on correlation energies.

Findings

Renormalization of QED-CC correlation energy and ground state by CS transformation.

Breakdown of origin invariance for charged systems due to dipole-dependent renormalization.

Divergent correlation energy in the low-frequency limit for molecules with non-zero dipole moments.

Abstract

We analyse the coherent-state (CS) transformation in quantum electrodynamics coupled cluster (QED-CC) theory from the perspective of its non-vanishing commutator with the polaritonic cluster operator. Specifically, we show that a QED Hartree-Fock (QED-HF) reference state parametrized by the CS transformation leads to a QED-CC Lagrangian formally determined by CS-representations of polaritonic Hamiltonian, polaritonic cluster and polaritonic deexcitation operators. Moreover, the herein proposed approach differs from the original formulation of QED-CC theory in the definition of the photon state basis and exploits photon-added coherent states in contrast to previously considered displaced number states. We find a renormalization of both QED-CC correlation energy and QED-CC ground state induced by the CS transformation, which depends on the mean-field expectation value of the molecular dipole operator and therefore breaks origin invariance for charged systems. Electronic contributions to correlation energy and QED-CC ground state are renormalized by CS-transformed mixed excitation and deexcitation operators. In contrast, the CS-transformed single-photon excitation affects only the QED-CC ground state but not directly the correlation energy. The renormalized QED-CC ansatz becomes similar to the original QED-CC formulation for large cavity frequencies leading to small renormalization corrections. A divergent correlation energy for molecules with a non-vanishing molecular dipole moment is found in the low-frequency limit, which we discuss with respect to multi-photon excitations in the polaritonic cluster operator and the relevance of the cavity-Born-Oppenheimer framework.