Radiative rotational lifetimes and state-resolved relative detachment cross sections from photodetachment thermometry of molecular anions in a cryogenic storage ring

Photodetachment thermometry on a beam of OH\(^-\) in a cryogenic storage ring cooled to below 10 K is carried out using two-dimensional, frequency and time dependent photodetachment spectroscopy over 20 minutes of ion storage. In equilibrium with the low-level blackbody field, we find an effective r...

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Veröffentlicht in:arXiv.org 2017-07
Hauptverfasser: Meyer, C, Becker, A, Blaum, K, Breitenfeldt, C, George, S, Göck, J, Grieser, M, Grussie, F, Guerin, E A, R von Hahn, Herwig, P, Krantz, C, Kreckel, H, Lion, J, Lohmann, S, Mishra, P M, Novotný, O, O'Connor, A P, Repnow, R, Saurabh, S, Schwalm, D, Schweikhard, L, Spruck, K, S Sunil Kumar, Vogel, S, Wolf, A
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Sprache:eng
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Zusammenfassung:Photodetachment thermometry on a beam of OH\(^-\) in a cryogenic storage ring cooled to below 10 K is carried out using two-dimensional, frequency and time dependent photodetachment spectroscopy over 20 minutes of ion storage. In equilibrium with the low-level blackbody field, we find an effective radiative temperature near 15 K with about 90% of all ions in the rotational ground state. We measure the J = 1 natural lifetime (about 193 s) and determine the OH\(^-\) rotational transition dipole moment with 1.5% uncertainty. We also measure rotationally dependent relative near-threshold photodetachment cross sections for photodetachment thermometry.
ISSN:2331-8422
DOI:10.48550/arxiv.1707.04889