http://arxiv.org/abs/1902.01759
We use the time-independent quantum-mechanical formulation of reactive collisions in order to investigate the state-to-state $\mathrm{H}^+ + \mathrm{HD} \to \mathrm{D}^+ + \mathrm{H}_2$ chemical reaction. We compute cross sections for collision energies up to 1.8 electron-volts and rate coefficients for temperatures up to 10000 kelvin. We consider HD in the lowest vibrational level $v=0$ and rotational levels $j=0$ to 4, and H$_2$ in vibrational levels $v’=0$ to 3 and rotational levels $j’=0$ to 9. For temperatures below 4000 kelvin, the rate coefficients strongly vary with the initial rotational level $j$, depending on whether the reaction is endothermic ($j\le 2$) or exothermic ($j\ge 3$). The reaction is also found less and less probable as the final vibrational quantum number $v’$ increases. Our results illustrate the importance of studying state-to-state reactions, in the context of the chemistry of the primordial universe.
M. Lepers, G. Guillon and P. Honvault
Wed, 6 Feb 19
54/65
Comments: 7 pages, 9 figures
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