1. CsAr, CsXe, and RbXe B 2 Σ 1/2 + Interatomic Potentials Determined from Absorption Spectra and Calculations of Franck-Condon Factors for Free-Free Optical Transitions of Atomic Collision Pairs.
- Author
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Hewitt JD, Campbell C, Raymond KT, Park S, Desai KV, Mironov AE, and Eden JG
- Abstract
Interatomic potentials for the B
2 Σ1/2 + states of CsAr, CsXe, and RbXe have been determined through comparisons of experimental B ← X absorption spectra for alkali vapor-rare gas mixtures with calculations of the Franck-Condon factors (FCFs) associated with free-free transitions of thermal atomic pairs. Simulations of optical transitions of alkali-rare gas atomic pairs between the thermal and vibrational continua of the X2 Σ1/2 + and B2 Σ1/2 + states of the molecule, responsible for the blue satellites of the Cs and Rb D2 resonance lines in a rare gas background, require the incorporation of ground-state J values above ∼400 into the FCF calculations and proper normalization of the free-particle wave functions. Absorption spectra computed on the basis of several X and B state interatomic potentials available in the literature were found to be sensitive to the height of the B2 Σ1/2 + state barrier, as well as the X2 Σ1/2 + state repulsive wall contour and the location of the van der Waals minimum. Other spectral simulations entailed iterative modifications to a selected B2 Σ1/2 + interatomic potential, again coupled with comparison to experimental B ← X spectra. Comparisons of calculated spectra with experiment yield a CsXe B2 Σ1/2 + potential, for example, exhibiting a barrier height of 76 cm-1 at 5.2 Å and yet is nearly flat at smaller values of internuclear separation ( R ). The latter contrasts with previous theoretical calculations of VB ( R ) in the vicinity of the barrier maximum. For the CsAr molecule, the B2 Σ1/2 + barrier height was found to be 221 cm-1 , which is within 3% of the value determined from pseudopotential calculations incorporating the spin-orbit effect. Reproducing Cs-rare gas experimental absorption spectra also requires the existence of a broad, shallow potential well lying beyond the B2 Σ1/2 + barrier that, for CsAr, has a dissociation energy ( De ∼ 24 cm-1 ) a factor of 3 larger than values predicted by theory. Similar results are obtained for the RbXe and CsXe complexes.- Published
- 2023
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