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$\Lambda$-enhanced gray-molasses loading and EIT cooling of neutral atoms in nanophotonic traps

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abstract

Nanophotonic traps for cold atoms typically have trap volumes that are orders of magnitude smaller than, e.g., free-space optical tweezers. This makes efficient loading of these traps challenging, thereby limiting the total number of atoms coupled to the nanophotonic waveguide. Here, we demonstrate that $\Lambda$-enhanced gray-molasses ($\Lambda$GM) can substantially increase the number of trapped atoms in a nanofiber-based cold-atom setup. Specifically, we observe a six-fold increase in the number of loaded atoms compared to conventional red-detuned polarization gradient cooling. Despite the unusually small depth of our optical trap of only 24 $\mu$K, we load about 4000 individual Cesium atoms, achieving optical depths exceeding 140 and reaching the collisional blockade regime over a length of approximately 1 mm. After loading, we perform efficient EIT-assisted cooling that is found to increase the trap storage time to 400(9) ms. This is a 5-fold improvement over the passive storage time. Remarkably, EIT-cooling also works with two co-propagating nanofiber-guided light fields and requiries only about a few hundred picowatt of optical power. Our results provide an efficient method to boost both the number of loaded atoms and the storage time of nanophotonic atom traps.

years

2026 1

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UNVERDICTED 1

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Surface charges in a Rydberg atom-nanowaveguide hybrid quantum system

physics.atom-ph · 2026-07-01 · unverdicted · novelty 5.0

Surface charges on the nanofiber, generated via Rydberg-ground state collisional ionization enhanced by dipole trapping fields, produce time-evolving spectral features in Rydberg excitation that are suppressed by an external oscillating electric field.

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  • Surface charges in a Rydberg atom-nanowaveguide hybrid quantum system physics.atom-ph · 2026-07-01 · unverdicted · none · ref 31 · internal anchor

    Surface charges on the nanofiber, generated via Rydberg-ground state collisional ionization enhanced by dipole trapping fields, produce time-evolving spectral features in Rydberg excitation that are suppressed by an external oscillating electric field.