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This research details how strong ro-vibrational van der Waals interactions in ultracold polar molecules can suppress collisional loss, enabling evaporative cooling of Fermi mixtures without external shielding. The findings offer significant potential for advancing quantum simulation and impurity physics by stabilizing fermionic molecules within optical lattices and controlling synthetic dimensions.
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Ro-vibrational van der Waals interaction between ultracold polar molecules

arXiv2 min read

arXiv:2607.25774v1 Announce Type: cross Abstract: We describe the ro-vibrational van der Waals interaction between ultracold polar molecules. This interaction is strong, leading to fast elastic collisions and orders of magnitude suppression of collisional loss. This enables evaporative cooling of Fermi mixtures of molecules in different ro-vibrational states, without active shielding by applying external fields. The scheme is compatible with microwave shielding, where it enables controlled state dependent interactions, opening up new opportunities for quantum simulation and impurity physics. The interaction can also be used to stabilize fermionic molecules in optical lattices, to control interactions in synthetic dimensions, for enhanced tweezer loading, and direct infrared shielding.

Abstract:We describe the ro-vibrational van der Waals interaction between ultracold polar molecules. This interaction is strong, leading to fast elastic collisions and orders of magnitude suppression of collisional loss. This enables evaporative cooling of Fermi mixtures of molecules in different ro-vibrational states, without active shielding by applying external fields. The scheme is compatible with microwave shielding, where it enables controlled state dependent interactions, opening up new opportunities for quantum simulation and impurity physics. The interaction can also be used to stabilize fermionic molecules in optical lattices, to control interactions in synthetic dimensions, for enhanced tweezer loading, and direct infrared shielding.

Quantum Gases (cond-mat.quant-gas); Atomic Physics (physics.atom-ph); Chemical Physics (physics.chem-ph); Quantum Physics (quant-ph)

arXiv:2607.25774 [cond-mat.quant-gas]

(or arXiv:2607.25774v1 [cond-mat.quant-gas] for this version)

https://doi.org/10.48550/arXiv.2607.25774 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 203 words

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