Lifetimes of ultra-long-range strontium Rydberg molecules

Abstract

The lifetimes of the lower-lying vibrational states of ultralong-range strontium Rydberg molecules comprising one ground-state 5s2 1S0 atom and one Rydberg atom in the 5s38s 3S1 state are reported. The molecules are created in an ultracold gas held in an optical dipole trap and their numbers determined using field ionization, the product electrons being detected by a microchannel plate. The measurements show that, in marked contrast to earlier measurements involving rubidium Rydberg molecules, the lifetimes of the low-lying molecular vibrational states are very similar to those of the parent Rydberg atoms. This results because the strong p-wave resonance in low-energy electronrubidium scattering, which plays an important role in determining the molecular lifetimes, is not present for strontium. The absence of this resonance offers advantages for experiments involving strontium Rydberg atoms as impurities in quantum gases and for testing theories of molecular formation and decay.

References in corpus (6)

• Production of trilobite Rydberg molecule dimers with thousand-Debye permanent electric dipole moments
• Ultracold atom-electron interaction: from two to many-body physics
• Experimental characterization of singlet scattering channels in long-range Rydberg molecules
• Ionization of Sodium and Rubidium nS, nP and nD Rydberg atoms by blackbody radiation
• Mass scaling and non-adiabatic effects in photoassociation spectroscopy of ultracold strontium atoms
• Hybridization of Rydberg electron orbitals by molecule formation

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