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This paper advances the equation-of-motion (EOM) formalism by extending it from independent-particle references to correlated many-body states, enabling a unified treatment of ground-state and excited-state dynamics in atomic nuclei. While primarily focused on nuclear spectroscopy, the methodology is explicitly motivated by its potential efficiency for quantum chemistry and quantum computing applications regarding excitation spectra. The work represents significant theoretical progress in handling strongly correlated systems within an ab initio framework relevant to future quantum algorithms.
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Revisiting the Equation-of-Motion Method: A Universal Framework for Correlated Quantum Systems

arXiv2 min read

arXiv:2607.29396v1 Announce Type: cross Abstract: A general implementation of the equation-of-motion (EOM) formalism for correlated many-body states is presented and applied to the description of collective excitations in atomic nuclei. While EOM approaches are traditionally formulated on top of independent-particle reference states, the present work extends the method to correlated reference states generated by modern many-body solvers. This formulation enables a consistent treatment of ground-state correlations and excited-state dynamics within a unified framework. Particular emphasis is placed on collective nuclear excitations employing chiral nuclear Hamiltonians in an ab initio context. The approach is motivated by the renewed interest in EOM techniques across several fields, including quantum chemistry and quantum computing, where they provide efficient and systematically improvable descriptions of excitation spectra. The present results demonstrate that the EOM framework offers a flexible and powerful tool for the microscopic description of nuclear spectroscopy beyond the traditional mean-field paradigm.

Abstract:A general implementation of the equation-of-motion (EOM) formalism for correlated many-body states is presented and applied to the description of collective excitations in atomic nuclei. While EOM approaches are traditionally formulated on top of independent-particle reference states, the present work extends the method to correlated reference states generated by modern many-body solvers. This formulation enables a consistent treatment of ground-state correlations and excited-state dynamics within a unified framework. Particular emphasis is placed on collective nuclear excitations employing chiral nuclear Hamiltonians in an ab initio context. The approach is motivated by the renewed interest in EOM techniques across several fields, including quantum chemistry and quantum computing, where they provide efficient and systematically improvable descriptions of excitation spectra. The present results demonstrate that the EOM framework offers a flexible and powerful tool for the microscopic description of nuclear spectroscopy beyond the traditional mean-field paradigm.

Nuclear Theory (nucl-th); Strongly Correlated Electrons (cond-mat.str-el); Chemical Physics (physics.chem-ph); Quantum Physics (quant-ph)

arXiv:2607.29396 [nucl-th]

(or arXiv:2607.29396v1 [nucl-th] for this version)

https://doi.org/10.48550/arXiv.2607.29396 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 246 words

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