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Main Authors: Weight, Braden M., Pei, Zheng, Tretiak, Sergei
Format: Preprint
Published: 2026
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Online Access:https://arxiv.org/abs/2603.18228
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author Weight, Braden M.
Pei, Zheng
Tretiak, Sergei
author_facet Weight, Braden M.
Pei, Zheng
Tretiak, Sergei
contents In computational chemistry of molecular materials, strong static correlation effects appear when electronic states, often involving the ground state, become quasi-degenerate, as occurs, for example, in bond-breaking processes. Such situations present significant challenges for accurate theoretical treatment. In these regimes, many-body methods involving a single-determinant description, such as Hartree-Fock theory and its time-dependent extension, fail to reproduce the correct topology of the ground and excited state potential energy surfaces (e.g., near conical intersections). When strongly correlated electronic systems are further strongly coupled to a quantized radiation field within the framework of non-relativistic cavity quantum electrodynamics, an additional photonic degree of freedom introduces both new complexity and new opportunities to control. Excited cavity photons can modify bond-breaking processes and enable tunability of geometrical and spin-phase transitions, for instance, in organometallic complexes. To overcome this bottleneck, in this work, we extend the well-studied spin-flip configuration interaction singles (SF-CIS) approach to explicitly include quantized cavity photons leading to QED-SF-CIS method. We derive the spin-flip Hamiltonian and find that the double excitation subspace of the system (single with respect to electronic excitation) must be included in the configurations to properly describe singlet electronic states interacting with cavity photons. We then illustrate, through representative molecular examples, how cavity coupling can provide additional tunability in bond-breaking processes. We finally generalize this approach to include higher numbers of photonic excitations, which are required in the strong coupling regime.
format Preprint
id arxiv_https___arxiv_org_abs_2603_18228
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Spin-Flip Configuration Interaction for Strong Static Correlation in Quantum Electrodynamics
Weight, Braden M.
Pei, Zheng
Tretiak, Sergei
Chemical Physics
In computational chemistry of molecular materials, strong static correlation effects appear when electronic states, often involving the ground state, become quasi-degenerate, as occurs, for example, in bond-breaking processes. Such situations present significant challenges for accurate theoretical treatment. In these regimes, many-body methods involving a single-determinant description, such as Hartree-Fock theory and its time-dependent extension, fail to reproduce the correct topology of the ground and excited state potential energy surfaces (e.g., near conical intersections). When strongly correlated electronic systems are further strongly coupled to a quantized radiation field within the framework of non-relativistic cavity quantum electrodynamics, an additional photonic degree of freedom introduces both new complexity and new opportunities to control. Excited cavity photons can modify bond-breaking processes and enable tunability of geometrical and spin-phase transitions, for instance, in organometallic complexes. To overcome this bottleneck, in this work, we extend the well-studied spin-flip configuration interaction singles (SF-CIS) approach to explicitly include quantized cavity photons leading to QED-SF-CIS method. We derive the spin-flip Hamiltonian and find that the double excitation subspace of the system (single with respect to electronic excitation) must be included in the configurations to properly describe singlet electronic states interacting with cavity photons. We then illustrate, through representative molecular examples, how cavity coupling can provide additional tunability in bond-breaking processes. We finally generalize this approach to include higher numbers of photonic excitations, which are required in the strong coupling regime.
title Spin-Flip Configuration Interaction for Strong Static Correlation in Quantum Electrodynamics
topic Chemical Physics
url https://arxiv.org/abs/2603.18228