Photoionization of vibrationally excited molecular hydrogen

Abstract
Cross sections for the photoionization of H2(XΣg+1, vi) in vibrational levels vi=014 are determined for a range of photon energies by a two-center treatment in which the derived electronic matrix elements are averaged over the initial and final vibrational states of the molecule and the molecular ion. Very good agreement with available measurements for vi=0 is obtained. Cross sections for the full Franck-Condon array of accessible transitions H2(vi)H2+(vf) are also presented. In the energy range considered, when the 2pσu dissociative state of H2+ is inaccessible, substantial contributions (up to 50% for vi=610) to the photoionization originate from H+ atomic ions which are formed via transitions to the vibrational continuum associated with the 1sσg state of H2+. Single-center and fixed-nuclei approximations which permit great simplification to the present treatment are also fully investigated.