关键词: 多组态含时Hartree-Fock/
电子关联/
强场电离/
氢分子
English Abstract
Multiconfiguration time-dependent Hartree-Fock treatment of electron correlation in strong-field ionization of H2 molecules
Zhang Bin1,Zhao Jian1,
Zhao Zeng-Xiu2
1.Northwest Institute of Nuclear Technology, Xi'an 710024, China;
2.Department of Physics, National University of Defense Technology, Changsha 410073, China
Fund Project:Project supported by the National Basic Research Program of China (Grant No. 2013CB922203), the National Natural Science Foundation of China (Grant No. 11374366), the Innovation Foundation of NUDT, China (Grant No. B110204), and the Hunan Provincial Innovation Foundation For Postgraduate, China (Grant No. CX2011B010).Received Date:20 December 2017
Accepted Date:10 March 2018
Published Online:20 May 2019
Abstract:Electron correlation plays an important role in the multielectron interactions of many physical and chemical processes.The investigation of correlation effects in the non-perturbative electronic dynamics (e.g.non-sequential double ionization) when atoms and molecules are subjected to strong laser fields requires non-perturbative theoretical treatments. The direct numerical integration of the time-dependent Schrödinger equation successfully explains many experimental results,but it is computationally prohibitive for systems with more than two electrons.There is clearly a need for a theory which can treat correlation dynamics self-consistently in strong time-dependent electric fields.In this paper we develop a three-dimensional multiconfiguration time-dependent Hartree-Fock method,which can be applied to the non-perturbative electronic dynamics for diatomic molecules,and it can also investigate the effect of electron correlation in strong-field ionization of H2 molecules.This method adopts the prolate spheroidal coordinates (which can treat the two-center Coulomb potential accurately) and the finite-element method together with discrete-variable representation (which lowers the calculation burden from two-electron integrations).For the temporal propagation,we use the efficient short iterative Lanczos algorithm for the equation which governs the configuration expansion coefficients,while an eight-order Runge-Kutta (RK) method and an Bulirsch-Stoer (BS) extrapolation method,both with adaptive precision controls,are implemented to solve the nonlinear orbital equation.While both methods yield correct results,the BS method displays a better stability in the realtime propagation,while the RK method demands less computation.The alignment-dependent ionization probabilities of H2 molecules in intense extreme ultraviolet pulses are calculated.Comparisons between multi-configuration and single-configuration results show that electron correlation has little effect on the single ionization process,but it plays an important role in double ionization,leading to the decrease in the ionization probability.The double ionization probability from the single-configuration space 1σ is about three times larger that from 4σ1π.The ionization probability increases monotonically when the alignment angle increases from 0° to 90°, yielding a ratio of 2.6(1.5) between 90° and 0° for the double (single) ionization process.This method presents the basis for the future study of electron correlation in strong-field processes.
Keywords: multiconfiguration time-dependent Hartree-Fock/
electron correlation/
strong-field ionization/
hydrogen molecules
