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Ultracold molecules have been proposed as a candidate platform for quantum science and precision measurement because of their rich internal structures and interactions. Direct laser-cooling promises to be a rapid and efficient way to bring molecules to ultracold temperatures. However, for trapped molecules, laser-cooling to the quantum motional ground state remains an outstanding challenge. A technique capable of reaching the motional ground state is Raman sideband cooling, first demonstrated in trapped ions and atoms. Here we demonstrate Raman sideband cooling of CaF molecules trapped in an optical tweezer array. Our protocol does not rely on high magnetic fields and preserves the purity of molecular internal states. We measure a high ground-state fraction and achieve low motional entropy per particle. The low temperatures we obtain could enable longer coherence times and higher-fidelity molecular qubit gates, desirable for quantum information processing and quantum simulation. With further improvements, Raman sideband cooling will also provide a route to quantum degeneracy of large molecular samples, which could be extendable to polyatomic molecular species.
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An optical tweezer array of ultracold polyatomic molecules
Polyatomic molecules have rich structural features that make them uniquely suited to applications in quantum information science1–3, quantum simulation4–6, ultracold chemistry7 and searches for physics beyond the standard model8–10. However, a key challenge is fully controlling both the internal quantum state and the motional degrees of freedom of the molecules. Here we demonstrate the creation of an optical tweezer array of individual polyatomic molecules, CaOH, with quantum control of their internal quantum state. The complex quantum structure of CaOH results in a non-trivial dependence of the molecules’ behaviour on the tweezer light wavelength. We control this interaction and directly and non-destructively image individual molecules in the tweezer array with a fidelity greater than 90%. The molecules are manipulated at the single internal quantum state level, thus demonstrating coherent state control in a tweezer array. The platform demonstrated here will enable a variety of experiments using individual polyatomic molecules with arbitrary spatial arrangement.
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- Award ID(s):
- 2317134
- PAR ID:
- 10511603
- Publisher / Repository:
- Nature
- Date Published:
- Journal Name:
- Nature
- Volume:
- 628
- Issue:
- 8007
- ISSN:
- 0028-0836
- Page Range / eLocation ID:
- 282 to 286
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1038/s41586-024-07199-1
