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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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Direct laser cooling of a symmetric top molecule
Ultracold polyatomic molecules have potentially wide-ranging applications in quantum simulation and computation, particle physics, and quantum chemistry. For atoms and small molecules, direct laser cooling has proven to be a powerful tool for quantum science in the ultracold regime. However, the feasibility of laser-cooling larger, nonlinear polyatomic molecules has remained unknown because of their complex structure. We laser-cooled the symmetric top molecule calcium monomethoxide (CaOCH3), reducing the temperature of ~104molecules from 22 ± 1 millikelvin to 1.8 ± 0.7 millikelvin in one dimension and state-selectively cooling two nuclear spin isomers. These results demonstrate that the use of proper ro-vibronic transitions enables laser cooling of nonlinear molecules, thereby opening a path to efficient cooling of chiral molecules and, eventually, optical tweezer arrays of complex polyatomic species.
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- Award ID(s):
- 1806571
- PAR ID:
- 10191433
- Publisher / Repository:
- American Association for the Advancement of Science (AAAS)
- Date Published:
- Journal Name:
- Science
- Volume:
- 369
- Issue:
- 6509
- ISSN:
- 0036-8075
- Page Range / eLocation ID:
- p. 1366-1369
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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