Translational energy spectroscopy (TES) in the range 214–857 eV amu−1 has been
used to study the collision mechanisms involved in one-electron capture by slow
helium-like N5+ in both atomic and molecular hydrogen. In the case of N5+–H2 collisions,
our measurements show that non-dissociative electron capture leading to the N4+ (n = 3) states is
the main product channel at the higher impact energies with smaller contributions to the
N4+ (n = 4)
states. While this has also been observed in previous studies based on photon
emission spectroscopy (PES), there are substantial differences in both magnitude and
energy dependence between the TES and PES results. Theoretical predictions for n = 3 formation
are also in poor accord with experiment. Unlike previous PES measurements, the
present TES study has been able to identify the presence of dissociative one-electron
capture channels and two-electron autoionizing capture channels, both leading to N4+
(n = 2)
formation. Two-electron autoionizing electron capture is found to be the main
collision mechanism leading to N4+ ions at the lowest energies considered. Our
measurements of one-electron capture in N5+ + H(1s) are in excellent accord with
previous higher measurements based on PES and now provide a useful
extension to energies below 1 keV amu−1. In this case, only the N4+ (n = 4) and N4+
(n = 3)
product channels are observed, with contributions from the latter becoming
insignificant at our lowest energies.