Strong interference effects in the resonant Auger decay of atoms induced by intense X-Ray fields

The theory of resonant Auger decay of atoms in a high intensity coherent X-ray pulse is presented. The theory includes the coupling between the ground state and the resonance due to an intense X-ray pulse, taking into account the decay of the resonance and the direct photoionization of the ground state, both populating the final ionic states coherently. The theory also considers the impact of the direct photoionization of the resonance state itself which typically populates highly-excited ionic states. The combined action of the resonant decay and of the direct ionization of the ground state in the field induces a non-hermitian time-dependent coupling between the ground and the 'dressed' resonance stats. The impact of these competing processes on the total electron yield and on the 2s$^2$2p$^{4}(^1\mathrm{D})$3p $^2$P spectator and 2s$^1$2p$^{6}$ $^2$S participator Auger decay spectra of the Ne 1s$\to$3p resonance is investigated. The role of the direct photoionization of the ground state and of the resonance increases dramatically with the field intensity. This results in strong interference effects with distinct patterns in the electron spectra, different for the participator and spectator final states.Comment: 31 pages, 6 figure

Resonant Auger decay of the core-excited C∗^\astO molecule in intense X-ray laser fields

The dynamics of the resonant Auger (RA) process of the core-excited C$^\ast$O(1s$^{-1}\pi^\ast,v_r=0$) molecule in an intense X-ray laser field is studied theoretically. The theoretical approach includes the analogue of the conical intersections of the complex potential energy surfaces of the ground and `dressed' resonant states due to intense X-ray pulses, taking into account the decay of the resonance and the direct photoionization of the ground state, both populating the same final ionic states coherently, as well as the direct photoionization of the resonance state itself. The light-induced non-adiabatic effect of the analogue of the conical intersections of the resulting complex potential energy surfaces gives rise to strong coupling between the electronic, vibrational and rotational degrees of freedom of the diatomic CO molecule. The interplay of the direct photoionization of the ground state and of the decay of the resonance increases dramatically with the field intensity. The coherent population of a final ionic state via both the direct photoionization and the resonant Auger decay channels induces strong interference effects with distinct patterns in the RA electron spectra. The individual impact of these physical processes on the total electron yield and on the CO$^+(A^2\Pi)$ electron spectrum are demonstrated.Comment: 13 figs, 1 tabe