Elastic and inelastic processes in H++C2H2 collisions below the 1.5-keV regime

Abstract
Electron capture and direct elastic scattering in collisions of H+ ions with C2 H2 molecules are studied by using a molecular representation within a fully quantum-mechanical approach below 1.5 keV. Calculations are carried out at two different molecular configurations: (i) C00v symmetry, in which H+ approaches the H atom along a C—H bond in the acetylene (C2 H2), and (ii) C2v symmetry, in which H+ approaches perpendicularly toward the midpoint between two carbon atoms. We find that electron capture in the C00v symmetry configuration takes place preferentially over that in the C2v symmetry configuration at scattering angles above 15°. The results for the C2v and C00v symmetries are comparable in magnitude below 10°, although the C2v symmetry dominates slightly at still smaller angles. Hence, interferences arising from these molecular configurations in differential cross sections for electron capture and elastic scattering processes are strongly present at angles smaller than a few degrees. Accordingly, the total cross section for the C2v symmetry is larger by a factor of 3 at 1 keV, and the difference widens as the energy decreases to the eV regime. This is because in C2v symmetry, H+ can have a larger overlap with the charge distribution of the C2 H2 molecule, thus causing a stronger interaction. © 1996 The American Physical Society.