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 min of ion storage. In equilibrium with the low-level blackbody field, we find an effective radiati...

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Veröffentlicht in:Physical review letters 2017-07, Vol.119 (2), p.023202-023202
Hauptverfasser: Meyer, C, Becker, A, Blaum, K, Breitenfeldt, C, George, S, Göck, J, Grieser, M, Grussie, F, Guerin, E A, von Hahn, R, 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, Sunil Kumar, S, 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 min 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:1079-7114
DOI:10.1103/PhysRevLett.119.023202