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Second-scale rotational coherence and dipolar interactions in a gas of ultracold polar molecules

Gregory, Philip D.; Fernley, Luke M.; Tao, Albert Li; Bromley, Sarah L.; Stepp, Jonathan; Zhang, Zewen; Kotochigova, Svetlana; Hazzard, Kaden R. A.; Cornish, Simon L.

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Authors

Dr Phil Gregory p.d.gregory@durham.ac.uk
Assistant Professor - Royal Society University Research Fellow

Luke M. Fernley

Albert Li Tao

Sarah L. Bromley

Jonathan Stepp

Zewen Zhang

Svetlana Kotochigova

Kaden R. A. Hazzard



Abstract

Ultracold polar molecules combine a rich structure of long-lived internal states with access to controllable long-range anisotropic dipole–dipole interactions. In particular, the rotational states of polar molecules confined in optical tweezers or optical lattices may be used to encode interacting qubits for quantum computation or pseudo-spins for simulating quantum magnetism. As with all quantum platforms, the engineering of robust coherent superpositions of states is vital. However, for optically trapped molecules, the coherence time between rotational states is typically limited by inhomogeneous differential light shifts. Here we demonstrate a rotationally magic optical trap for 87Rb133Cs molecules that supports a Ramsey coherence time of 0.78(4) s in the absence of dipole–dipole interactions. This is estimated to extend to >1.4 s at the 95% confidence level using a single spin-echo pulse. In our trap, dipolar interactions become the dominant mechanism by which Ramsey contrast is lost for superpositions that generate oscillating dipoles. By changing the states forming the superposition, we tune the effective dipole moment and show that the coherence time is inversely proportional to the strength of the dipolar interaction. Our work unlocks the full potential of the rotational degree of freedom in molecules for quantum computation and quantum simulation.

Citation

Gregory, P. D., Fernley, L. M., Tao, A. L., Bromley, S. L., Stepp, J., Zhang, Z., …Cornish, S. L. (2024). Second-scale rotational coherence and dipolar interactions in a gas of ultracold polar molecules. Nature Physics, 20(3), 415-421. https://doi.org/10.1038/s41567-023-02328-5

Journal Article Type Article
Acceptance Date Nov 8, 2023
Online Publication Date Jan 17, 2024
Publication Date Mar 1, 2024
Deposit Date Feb 28, 2024
Publicly Available Date Feb 28, 2024
Journal Nature Physics
Print ISSN 1745-2473
Electronic ISSN 1745-2481
Publisher Nature Research
Peer Reviewed Peer Reviewed
Volume 20
Issue 3
Pages 415-421
DOI https://doi.org/10.1038/s41567-023-02328-5
Keywords General Physics and Astronomy
Public URL https://durham-repository.worktribe.com/output/2226730

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