Coherent control of isotope separation in HD+ photodissociation by strong fields.

Abstract

The photodissociation of the ${\mathrm{HD}}^{+}$ molecular ion in intense short-pulsed linearly polarized laser fields is studied using a time-dependent wave-packet approach where molecular rotation is fully included. We show that applying a coherent superposition of the fundamental radiation with its second harmonic can lead to asymmetries in the fragment angular distributions, with significant differences between the hydrogen and deuterium distributions in the long wavelength domain where the permanent dipole is most efficient. This effect is used to induce an appreciable isotope separation.