Electron rescattering and the fragmentation dynamics of molecules in strong optical fields

Abstract

We have probed the fragmentation dynamics in a bent triatomic molecule, water, a non-planar molecule, methanol, and a planar ring-structured molecule, benzene, using 100 fs duration pulses of linearly and circularly polarized, infrared, intensity-selected laser light. At laser intensities larger than 10$^{15}$ W cm$^{-2}$, the yield of singly and multiply charged atomic fragments from these molecules is suppressed when the light is circularly polarized. At lower intensities, the fragment ion yield is not significantly polarization dependent. This hitherto-unobserved intensity dependent effect of the polarization state of light on the fragmentation dynamics is rationalized using a simple electron rescattering model. Circular polarization switches "off" electron rescattering and leads to suppression of multiple ionization and molecular fragmentation. Moreover, the degree of suppression is dependent upon the amount of energy transfer from the optical field to the molecule: the larger the energy transfer that is required for a particular fragmentation channel, the more marked is its suppression when circular polarization is used.