Time-dependent Feshbach method to study resonant photoionization of He with ultrashort laser pulses

28th International Conference on Photonic, Electronic and Atomic Collisions

Sanz-Vicario, José Luis^1 ; Granados-Castro, Carlos Mario^1

Grupo de Física Atómica y Molecular, Instituto de Física, Universidad de Antioquia UdeA, Calle 70 No. 52-21, Medellín, Colombia^1

关键词: Electrostatic coupling;    Feshbach formalism;    Harmonic frequency;    Photoelectron angular distributions;    Resonance parameters;    Second ionization;    Temporal evolution;    Temporal formation;   

Others  :  https://iopscience.iop.org/article/10.1088/1742-6596/488/1/012018/pdf
DOI  :  10.1088/1742-6596/488/1/012018

来源: IOP

【 摘 要 】

A time-dependent Feshbach formalism is proposed to study the resonant photoionization of the helium atom using ultrashort laser pulses. This spectral method consist in solving the time-dependent Schrödinger equation by expanding the time-dependent wavepacket in terms of eigenfunctions defined in two orthogonal halfspaces: a bound-like resonant Q and a non-resonant scattering-like P. The latter eigenfunctions for the projected Hamiltonians QHQ and PHP are not indeed eigenfunctions of the total Hamiltonian, so that the electrostatic coupling QHP acts as a leaking operator Q!P responsible for the temporal decay of resonances into the underlying continuum, keeping the physical insight of the Fano-Feshbach time independent formalisms. This method allows not only for accurate descriptions of the resonance parameters (energies, widths and Fano shape parameters) but also for the temporal evolution of the photodynamics involved in the resonant photoionization when using short laser pulses. We illustrate the performance of the method by analyzing the temporal formation of i) the one-photon ionization cross section below the second ionization threshold and the buildup of Fano profiles and ii) the up-down asymmetry of photoelectron angular distributions resulting from interferences of S-, P- and D-waves after simultaneous photoexcitation and decay of the lowest1Se,1P0and1Deresonant states, by using two sequential laser pulses with XUV harmonic frequencies separated by a time delay.