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Phys. Rev. Lett. 95, 013003 (2005) [4 pages]

Direct Measurement of the Radiative Lifetime of Vibrationally Excited OH Radicals

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Sebastiaan Y. T. van de Meerakker1,2, Nicolas Vanhaecke1, Mark P. J. van der Loo3, Gerrit C. Groenenboom3, and Gerard Meijer1
1Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, 14195 Berlin, Germany
2FOM-Institute for Plasmaphysics Rijnhuizen, Edisonbaan 14, 3439 MN Nieuwegein, The Netherlands
3Institute of Theoretical Chemistry, University of Nijmegen, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands

Received 13 May 2005; published 1 July 2005

Neutral molecules, isolated in the gas phase, can be prepared in a long-lived excited state and stored in a trap. The long observation time afforded by the trap can then be exploited to measure the radiative lifetime of this state by monitoring the temporal decay of the population in the trap. This method is demonstrated here and used to benchmark the Einstein A coefficients in the Meinel system of OH. A pulsed beam of vibrationally excited OH radicals is Stark decelerated and loaded into an electrostatic quadrupole trap. The radiative lifetime of the upper Λ-doublet component of the X2Π3/2, v=1, J=3/2 level is determined as 59.0±2.0  ms, in good agreement with the calculated value of 58.0±1.0  ms.

© 2005 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevLett.95.013003
DOI:
10.1103/PhysRevLett.95.013003
PACS:
33.80.Ps, 33.70.Ca, 39.10.+j