Charge asymmetric dissociation induced by sequential and nonsequential strong field ionization

Charge asymmetric dissociation (CAD) is observed, for the first time, with near-infrared 30 fs laser pulses, in small molecules, N-2 and O-2. N-2(2+) is created by a nonsequential (vertical) transition and the dissociation fragments appear to be in excited states. Unlike N-2, O-2(2+) involves a sequential (nonvertical) transition. The charge asymmetric dipole coupling to the external field is insufficient to populate the charge transfer states leading to CAD. Rather, CAD is a natural result of strong field excitation and ionization. These results in the tunneling regime are also compared with previous experiments performed with UV radiation in the multiphoton regime.