Radiative cooling dynamics of isolated N2O+ ions in a cryogenic electrostatic ion storage ring

Abstract

We study radiative cooling processes of ${\mathrm{N}}_{2}{\mathrm{O}}^{+}$ ions isolated in vacuum by taking advantage of the extended storage times possible with a cryogenic electrostatic ion storage ring. The temporal evolution of the internal state populations of the ${\mathrm{N}}_{2}{\mathrm{O}}^{+}$ ions after being stored in the ring was state-selectively measured by action spectroscopy via a predissociation process using a wavelength-tunable pulsed laser. The rotational level population remained unchanged up to about 200 s after ion storage, which is consistent with theoretical predictions and the small permanent dipole moment. On the other hand, we found that depletion of the vibrational excited states in the NN-O stretching mode proceeded within 5 s, while a noticeable increase of the ground-state population was not observed. This implies that the initial populations of the vibrational excited states are relatively small. We discuss such behavior in the context of the initial population distribution of ions extracted from the ion source with a simulation based on simple cascade modeling.