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This research investigates the resonant coupling between the rotational states of thorium fluoride molecular ions and the vibrational modes of a trapped ytterbium ion crystal, advancing quantum control techniques for hybrid atomic-molecular systems. By accounting for hyperfine structure, the study establishes specific conditions for dipole-phonon interaction that could enable new protocols in quantum simulation and error correction using complex internal states.
A linear rotor trapped and coupled to the vibrational modes of an ion crystal
arXiv:2504.00590v2 Announce Type: replace Abstract: When molecular ions are trapped together with atomic ions in a Paul trap, their dipole moment couples the molecular rotation to the joint vibrational motion of the particles in the trap. To leverage this coupling for quantum control, a rotational transition in the molecule should be resonant with one of the ion crystal vibrational modes. Focusing on the example of singly charged thorium fluoride molecular ions, cotrapped with two ytterbium ions, we determine the conditions for resonant dipole-phonon coupling, fully accounting for the molecular hyperfine structure. We identify several choices for resonant coupling and discuss its detection using sideband-resolved laser spectroscopy and measurements of decoherence.
Abstract:When molecular ions are trapped together with atomic ions in a Paul trap, their dipole moment couples the molecular rotation to the joint vibrational motion of the particles in the trap. To leverage this coupling for quantum control, a rotational transition in the molecule should be resonant with one of the ion crystal vibrational modes. Focusing on the example of singly charged thorium fluoride molecular ions, cotrapped with two ytterbium ions, we determine the conditions for resonant dipole-phonon coupling, fully accounting for the molecular hyperfine structure. We identify several choices for resonant coupling and discuss its detection using sideband-resolved laser spectroscopy and measurements of decoherence.
Quantum Physics (quant-ph); Atomic Physics (physics.atom-ph)
arXiv:2504.00590 [quant-ph]
(or arXiv:2504.00590v2 [quant-ph] for this version)
https://doi.org/10.48550/arXiv.2504.00590 Focus to learn more arXiv-issued DOI via DataCite
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Full text under the publisher's open licence · 200 words
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