Strong-field polarizability-enhanced dissociative ionization

Abstract

We investigate dissociative single and double ionization of ${\mathrm{HeH}}^{+}$ induced by intense femtosecond laser pulses. By employing a semiclassical model with nuclear trajectories moving on field-dressed surfaces and ionization events treated as stochastical jumps, we identify a strong-field mechanism wherein the molecules dynamically align along the laser polarization axis and stretch towards a critical internuclear distance before dissociative ionization. As the tunnel-ionization rate is larger for larger internuclear distances and for aligned samples, ionization is enhanced. The strong dynamical rotation originates from the anisotropy of the internuclear distance-dependent polarizability tensor, which features a maximum at certain internuclear distances. Good qualitative agreement with our experimental observations is found. Finally, we investigate under which experimental conditions isotope effects of different isotopologues of ${\text{HeH}}^{+}$ can be observed.