A GLOBAL FIT OF THE $X^{3}\Sigma^{-}_{g}$, $a^{1}\Delta_{g}$, $b^{1}\Sigma^{+}_{g}$ AND $B^{3}\Sigma^{-}_{u}$ STATES OF THE SIX ISOTOPOLOGUES OF OXYGEN

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A global fit of the six isotopologues of the O2 molecule has been carried out, with the purpose to support the current and future Earth remote sensing missions. All previously available experimental data from the following systems were collected and used in the analysis: the microwave transitions in the X3Σg and a1Δg states, the infared transitions from the a1Δg X3Σg, b1Σg+ X3Σg, and b1Σg+ a1Δg systems, the UV transitions from the B3Σu X3Σg Schumann-Runge system. For the main 16O2 isotopologue, experimental data are available for the following vibrational states: v=0−18 for X3Σg, v=0−1 for a1Δg, v=0−17 for b1Σg+, v=0−17 for B3Σu. A band by band fit was first carried out for these 16O2 data to check bad measurements, misassigments and calibration problems. Then all these 16O2 data were fitted with a Dunham-type model. It was found that most 16O2 data (98%) could be fitted within 3 times experimental accuracies in the band by band fit; the X3Σg, a1Δg, b1Σg+ states could be well reproduced with the Dunham-type model; but the vibrational energies for v=0−17 of B3Σu could not be fitted well with the Dunham-type mode, probably caused by the known perturbations in this state. A band by band fit has been performed for each of the other five minor isotopologues, and a Dunham-type fit is in progress for these data. Eventually data from all the six isotopologues will be simultaneously fitted with a multi-isotopologue Dunham model. We will present the most recent fitting results to date.

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Author Institution: Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA 91109; I. Physikalisches Institut, Universitat zu Koln, 50937 Koln, Germany

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