Multipole-moment effects in ion-molecule reactions at low temperatures: part I -- Ion-dipole enhancement of the rate coefficients of the He+ + NH3 and He+ + ND3 reactions at collision energies near 0 K
Abstract
The energy dependence of the rates of the reactions between He+ and ammonia (NY3, Y= H,D), forming NY2+, Y and He as well as NY+, Y2 and He, and the corresponding product branching ratios have been measured at low collision energies between 0 and kB·40 K using a recently developed merged-beam technique [Allmendinger et al., ChemPhysChem 17, 3596 (2016)]. To avoid heating of the ions by stray electric fields, the reactions are observed within the large orbit of a highly excited Rydberg electron. A beam of He Rydberg atoms was merged with a supersonic beam of ammonia using a curved surface-electrode Rydberg-Stark deflector, which was also used for adjusting the final velocity of the He Rydberg atoms, and thus the collision energy (E coll). A collision-energy resolution of about 200 mK was reached at the lowest E coll values. The reaction rate coefficients exhibit a sharp increase at collision energies below kB·5 K and pronounced deviations from Langevin-capture behaviour. The experimental results are interpreted in terms of an adiabatic capture model describing the rotational-state-dependent orientation of the ammonia molecules by the electric field of the He+ atom. The model faithfully describes the experimental observations. The enhancement of the reaction yields of both reactions observed at the lowest collision energies is attributed to high-field-seeking states which experience linear Stark shifts at low electric fields. Thermal capture rate constants are derived from the model for the temperature range between 0 and 10~K relevant for astrochemistry. Comparison of the calculated thermal capture rate coefficients with the absolute reaction rates measured above 27 K by Marquette et al. (Chem. Phys. Lett., 1985, 122, 431) suggests that only 40\% of the close collisions are reactive.
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