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Journal of the Optical Society of America B

Collision-based spectroscopy of Xe VI Rydberg states (vol 13, pg 2715, 1996)

M Wang, MO Larsson, Arne Arnesen, Reinhold Hallin, Filip Heijkenskjöld, CARL NORDLING, Anders Wännström

Published Jan 1, 1996• 0 citations
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Optics Express•Sep 7, 2021•12 citations
The OODR mass spectroscopy is applied to investigate dynamical properties of Xe**Kr in high Rydberg states. It is found that two dissociation pathways producing both the Xe** and Kr** fragments compete, where the ion core of high Rydberg molecule switches. It is revealed that ion-core switching (ICS) occurs because of the interaction between bound potentials of high Rydberg states Xe**Kr and a repulsive potential of XeKr**. Moreover, the observed variation in ICS ratio is explained by the population transfer from high Rydberg states of Xe**Kr of the A ion core to those of the X ion-core.
Rather than being freed to the continuum, the strong-field tunneled electrons can make a trajectory driven by the remaining laser fields and have certain probability to be captured by the high lying Rydberg states of the parent atoms or molecules. To explore the effect of molecular orbital on Rydberg state excitation, the ellipticity dependence of Rydberg state yields of N2 and O2 molecules are experimentally investigated using cold target recoil ion momentum spectroscopy and are compared with their counterpart atoms Ar and Xe with comparable ionization potentials. We found the generation probability of the neutral Rydberg fragment O2* was orders of magnitude higher than that of Xe* due to the butterfly-shaped highest occupied molecular orbital of O2. Meanwhile, our experimental and simulation results reveal that it is the initial momentum distribution (determined by the detailed characteristics of orbitals) that finally leads to the tendency that the Rydberg state yield of O2 (Ar) decreased slower than that obtained for Xe (N2) when the ellipticity of the excitation laser field is increased.