IOP Publishing
Browse
jpb455013f8_online.jpg (179.54 kB)

Impact of the DICES on the rotational population of the neutral CO molecules remaining in their ground electronic state after the Gaussian-shaped pulse of 4 fs duration and carrier frequency of 534.2 eV have expired

Download (0 kB)
figure
posted on 2013-08-13, 00:00 authored by Ph V Demekhin, L S Cederbaum

Figure 8. Impact of the DICES on the rotational population of the neutral CO molecules remaining in their ground electronic state after the Gaussian-shaped pulse of 4 fs duration and carrier frequency of 534.2 eV have expired. Before the pulse arrived, the target CO molecules were isotropically oriented, i.e. in the ground rotational state J0 = 0. The populations of the J0 rotational levels for the v0 = 0 − 2 vibrational levels as a function of peak intensity computed exactly, i.e. DICES model and Total (no approximations) are shown. For each vibrational level v0, the sum of the populations of all rotational levels is normalized to 100% at each peak intensity.

Abstract

The dynamics of the resonant Auger (RA) decay of the core-excited CO*(1s−1π*) molecule in intense x-ray laser pulses is studied theoretically. The present approach includes the impact of the analogue of conical intersections of the complex potential energy surfaces of the ground and 'dressed' resonant states induced by intense x-ray pulses. It also takes 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 individual impacts of these physical processes on the total ion yield, the CO+(A2Π) electron spectrum and the ro-vibrational distributions of the neutral molecules remaining in the ground electronic state after the laser pulse has expired are analysed and compared to those reported previously for the C*O resonance. It is also demonstrated that the RA effect of molecules by strong laser pulses of resonant carrier frequency is an efficient process to produce two-site double-core-hole–one-particle states of CO*.

History

Usage metrics

    IOP Publishing

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC