Orthogonally polarized two-color sequential laser pulses are used to control the electron
localization in the dissociation of H 2+. The first single attosecond pulse, whose polarization …

The dissociation dynamics of LiH molecules induced by two overlapping femtosecond
pulses is investigated based on the time-dependent quantum wave packet method. The first …

The dissociation dynamics of molecular ion HD+ in two completely overlapping THz and
infrared pulses are investigated by using the time-dependent quantum wave packet method …

The possibility of controlling fragment branching in the dissociation and ionization channels
of HD+ is theoretically explored by synthesized intense fields using 790 nm and 395 nm …

We systematically study the influence of laser intensities on the dissociation of H 2+ in strong
laser fields by numerically solving the time-dependent Schrödinger equation. In Ti: sapphire …

H (2 S)+ Cl+(1 D) steered by intense femtosecond laser pulses are investigated theoretically
using the quantum wave packet dynamics. The numerical calculations are performed in two …

The dissociation of the molecular ion HD+ in moderate-intensity laser pulses is studied
using the time-dependent quantum wave-packet method. Simulations of the time-of-flight …

We have numerically explored the possibility of controlling the branching ratio of the two
distinguishable photodissociation products of HD+(neutral D and neutral H) in an ultrashort …

Above-threshold dissociation (ATD) process of the molecular ions HD+ steered by a
femtosecond laser pulse train (LPT) is investigated theoretically using the time-dependent …

A theoretical scheme is proposed to study the influence of molecular orientation on the
photodissociation of LiH molecules based on time-dependent quantum wave packet theory …