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In this work, we apply the Monte Carlo wave packet method to study the ultrafast nuclear dynamics following inner-shell photoionization of N2 exposed to an ultrashort intense X-ray pulse. The photon energy of the X-ray pulse is large enough to remove a 1s electron from the N atom in N2. The intermediate state in N+2 is highly excited so that autoionization takes place from this state to the dissociative or non-dissociative electronic states of ungerade and gerade symmetries in N++2. The possible vibrational resonances allowed by the non-dissociative states prevents a direct extraction of the nuclear kinetic release (KER) spectrum from the nuclear wave packets in N++2. Therefore, we propose a hybrid technique by combining the advantages of two energy analysis strategies to obtain the final nuclear KER spectrum of the process. A femtosecond IR probe pulse, which couples the electronic states in N++2 together, is applied to achieve a time-resolved imaging and controlling of the ultrafast dynamics that takes place during double ionization of N2. The influence of the laser parameters including the peak intensity, pulse duration and pump-probe delay, on the nuclear dynamics is also investigated.
We discuss the complicated resonance structure of the endohedral atom photoionization cross section. Very strong enhancement and interference patterns in the photoionization cross-section of the valent and subvalent subshells of noble gas endohedral
We demonstrate rather interesting manifestations of co-existence of resonance features in characteristics of the photoionization of 3d-electrons in Xe@C60. It is shown that the reflection of photoelectrons produced by the 3d Xe photoionization affect
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The acetylene-vinylidene system serves as a benchmark for investigations of ultrafast dynamical processes where the coupling of the electronic and nuclear degrees of freedom provides a fertile playground to explore the femto- and sub-femto-second phy
We investigate the linear behavior in the 2+ ion concentration observed in the double photoionization of a variety of aromatic molecules. We show it arises when the photoelectrons are emitted simultaneously. Neglecting the momentum of the incoming ph