Non-adiabatic decay of Rydberg-atom-ion molecules
arXiv:2108.10475 · doi:10.1103/PhysRevA.105.012810
Abstract
The decay of Rydberg-atom-ion molecules (RAIMs) due to non-adiabatic couplings between electronic potential energy surfaces is investigated. We employ the Born-Huang representation and perform numerical simulations using a Crank-Nicolson algorithm. The non-adiabatic lifetimes of rubidium RAIMs for the lowest ten vibrational states, , are computed for selected Rydberg principal quantum numbers, . The non-adiabatic lifetimes are found to generally exceed the radiative Rydberg-atom lifetimes. We observe and explain a trend of the lifetimes as a function of and , and attribute irregularities to quantum interference arising from a shallow potential well in an inner potential surface. Our results will be useful for future spectroscopic studies of RAIMs.
7 pages, 3 figures, 1 table
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Cited by in corpus (6)
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- Non-adiabatic interaction effects in the spectra of ultralong-range Rydberg molecules
- Charged ultralong-range Rydberg trimers
- Nonadiabatic decay of metastable states on coupled linear potentials