In this work, a previous quantum wave-packet time-dependent study (D. De Fazio, A. Aguado and C. Petrongolo, Non-adiabatic quantum dynamics of the dissociative charge transfer He+ + H2 → He + H + H+. Front. Chem., 2019, 7, A249) on the charge-transfer dissociation of the hydrogen molecule by the helium cation is continued, extending the calculation to eight rotational H2 reactant states. New data are required to obtain convergent (within about 1 percent) Boltzmann-averaged thermal rate constants up to 1000 Kelvin, which are necessary to provide reliable reaction yields for astrophysical and cosmological computational models. To the best of our knowledge, these are the first quantum mechanical thermal rate constant calculations for a dissociative charge transfer process. As shown in the previous work for the effect of vibrations, a relevant role of rotations is found, and the use of roto-vibrational ground state rate constant only, as often employed in astrophysical model is a poor approximation, especially above room temperature. The large computational scaling of wave-packet methods for excited rotational reactant states, due to the linear increase of the number of projections of the diatomic rotational angular momentum along the internuclear axis, is handled efficiently in the calculations, providing an accurate documentation for developing approximations that are needed to extend the calculations to higher temperatures. A particular effort has been made to better clarify the reaction mechanism, which indicated the key roles of the geometrical phase and non-adiabatic effects. Additionally, the rich resonance pattern, which is the principal reaction mechanism at these temperatures and represents the main source of the computational load, is analyzed and rationalized in detail according to the resonance analysis.
Fazio et al. (Thu,) studied this question.