Excitation and characterization of long-lived hydrogenic Rydberg states of nitric oxide
arXiv:2005.00090 · doi:10.1063/5.0003092
Abstract
High Rydberg states of nitric oxide (NO) with principal quantum numbers between 40 and 100 and lifetimes in excess of 10 s have been prepared by resonance enhanced two-color two-photon laser excitation from the X ground state through the A intermediate state. Molecules in these long-lived Rydberg states were detected and characterized 126 s after laser photoexcitation by state-selective pulsed electric field ionization. The laser excitation and electric field ionization data were combined to construct two-dimensional spectral maps. These maps were used to identify the rotational states of the NO ion core to which the observed series of long-lived hydrogenic Rydberg states converge. The results presented pave the way for Rydberg-Stark deceleration and electrostatic trapping experiments with NO, which are expected to shed further light on the decay dynamics of these long-lived excited states, and are of interest for studies of ion-molecule reactions at low temperatures.
arXiv comment12 pages, 10 figures
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Cited by in corpus (6)
- A method for the variational calculation of hyperfine-resolved rovibronic spectra of diatomic molecules
- Slow decay processes of electrostatically trapped Rydberg NO molecules
- Ultralong-range Rydberg bi-molecules
- A spectroscopic model for the low-lying electronic states of NO
- Electrostatic trapping of N molecules in high Rydberg states
- The Stark effect in molecular Rydberg states: Calculation of Rydberg-Stark manifolds of H and D including fine and hyperfine structures