Origin of fine structures on the dissociative 1 s→ σ∗ resonance in X-ray absorption spectra of O 2

Abstract

We attempt to explain a puzzling long-tailed peak shape of the X-ray absorption spectrum of the oxygen molecule in the energy region around 539 eV taking into account the Rydberg–valence and vibronic couplings. The long-tailed feature is found to arise from two dissociative σ ∗ states and the sudden drop in intensity is related to decrease in transition dipole near the crossing point between the repulsive σ ∗ and weak 3 s Rydberg states with the quartet ion cores. This is supported by numerical wave-packet simulations allowing for all interchannel couplings between the Rydberg and valence manifolds with the quartet and doublet ion cores in a diabatic representation of the core-excited states.