Abstract
We demonstrate a versatile, state-dependent trapping scheme for the ground and first excited rotational states of molecules. Close to the rotational manifold of a narrow electronic transition, we determine tune-out frequencies where the polarizability of one state vanishes while the other remains finite, and a magic frequency where both states experience equal polarizability. The proximity of these frequencies of only 10 GHz allows for dynamic switching between different trap configurations in a single experiment, while still maintaining sufficiently low scattering rates.
- Received 21 December 2019
- Accepted 15 June 2020
DOI:https://doi.org/10.1103/PhysRevLett.125.023201
Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI. Open access publication funded by the Max Planck Society.
Published by the American Physical Society