An ab initio simulation of strong-field photodissociation of diatomic molecules was developed, inspired by recent dissociation experiments of F2-. The transition between electronic states was modeled, including the laser pulse and transition dipole, and the angle between them. The initial conditions of the system were set to be thermal and to include different rovibrational states. Carefully designed absorbing boundary conditions were applied to describe the boundary conditions of the experiment. We studied the influence of field intensity on the direction of the outcoming fragments and laboratory-fixed axis, defined by the field polarization. At high intensities, the angular distribution became more peaked with a marginal influence on kinetic energy release.

生成讲解博客的中文版本

生成AI智能校验的中文版本