Extending rotational coherence of interacting polar molecules in a spin-decoupled magic trap
Frauke See{\ss}elberg, Xin-Yu Luo, Ming Li, Roman Bause, Svetlana, Kotochigova, Immanuel Bloch, Christoph Gohle

TL;DR
This paper demonstrates a significant extension of rotational coherence times in polar molecules by employing spin-decoupled magic trapping, reducing light shifts, and analyzing dipolar interaction effects in a dilute gas.
Contribution
It introduces a novel spin-decoupled magic trapping technique that nearly doubles the rotational coherence time in polar molecules.
Findings
Rotational coherence time extended to 8.7 ms
Spin-decoupled magic trapping reduces light shifts
Dipolar interactions cause density-dependent coherence times
Abstract
Superpositions of rotational states in polar molecules induce strong, long-range dipolar interactions. Here we extend the rotational coherence by nearly one order of magnitude to 8.7(6) ms in a dilute gas of polar NaK molecules in an optical trap. We demonstrate spin-decoupled magic trapping, which cancels first-order and reduces second-order differential light shifts. The latter is achieved with a dc electric field that decouples nuclear spin, rotation and trapping light field. We observe density-dependent coherence times, which can be explained by dipolar interactions in the bulk gas.
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