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This paper derives a classical-limit formula for matrix elements between bound states of distinct one-dimensional potentials, validating its accuracy against analytical solutions in the classical regime. The research specifically targets applications in modeling atoms within optical lattices to enhance the precision of next-generation optical lattice clocks. While rooted in fundamental quantum mechanics and atomic physics, this work directly supports advancements in high-precision quantum sensing technologies.
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Classical-limit formula for matrix elements between bound states of distinct one-dimensional potentials

arXiv2 min read

arXiv:2608.16835v1 Announce Type: new Abstract: A classical-limit formula is derived for matrix elements between bound states of distinct one-dimensional potentials. We leave open the physical interpretation of the potentials, but generally envision them to be Born-Oppenheimer-type potentials with the position variable $x$ identifying with a slowly evolving degree of freedom of the system. For instance, $x$ could represent the internuclear separation in a diatomic molecule, with the potentials being potential energy curves for different electronic states. In this scenario, the matrix elements could be, e.g., conventional Franck-Condon factors. To test the derived formula, we assume functional forms for the potentials and operator that afford analytical solutions for the matrix elements. As the classical limit is approached, the computed matrix elements exhibit a clear tendency towards the classical-limit formula, providing strong validation for the formula. In future work, we anticipate using the formula to model inhomogeneous excitation spectra of atoms in one-dimensional optical lattices, with an eye towards improved optical lattice clock performance.

Abstract:A classical-limit formula is derived for matrix elements between bound states of distinct one-dimensional potentials. We leave open the physical interpretation of the potentials, but generally envision them to be Born-Oppenheimer-type potentials with the position variable $x$ identifying with a slowly evolving degree of freedom of the system. For instance, $x$ could represent the internuclear separation in a diatomic molecule, with the potentials being potential energy curves for different electronic states. In this scenario, the matrix elements could be, e.g., conventional Franck-Condon factors. To test the derived formula, we assume functional forms for the potentials and operator that afford analytical solutions for the matrix elements. As the classical limit is approached, the computed matrix elements exhibit a clear tendency towards the classical-limit formula, providing strong validation for the formula. In future work, we anticipate using the formula to model inhomogeneous excitation spectra of atoms in one-dimensional optical lattices, with an eye towards improved optical lattice clock performance.

Quantum Physics (quant-ph); Atomic Physics (physics.atom-ph)

arXiv:2608.16835 [quant-ph]

(or arXiv:2608.16835v1 [quant-ph] for this version)

https://doi.org/10.48550/arXiv.2608.16835 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

APS Open Sci. 1, 000077 (2026)

https://doi.org/10.1103/kyjq-2fc4 Focus to learn more DOI(s) linking to related resources

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Full text under the publisher's open licence · 270 words

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