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arXiv 2015-08-31 DOI 10.3847/0004-637X/816/1/31 0 views

Merged-beams Reaction Studies of O + H₃+

de Ruette, N. · Miller, K. A. · O'Connor, A. P. · Urbain, X. · Buzard, C. F. · Vissapragada, S. · Savin, D. W.

Original · EN

We have measured the reaction of O + H3+ forming OH+ and H2O+. This is one of the key gas-phase astrochemical processes initiating the formation of water molecules in dense molecular clouds. For this work, we have used a novel merged fast-beams apparatus which overlaps a beam of H3+ onto a beam of ground-term neutral O. Here, we present cross section data for forming OH+ and H2O+ at relative energies from ≈ 3.5 meV to ≈ 15.5 and 0.13 eV, respectively. Measurements were performed for statistically populated O(3PJ) in the ground term reacting with hot H3+ (with an internal temperature of ≈ 2500-3000 K). From these data, we have derived rate coefficients for translational temperatures from ≈ 25 K to ≈ 10⁵ and 10³ K, respectively. Using state-of-the-art theoretical methods as a guide, we have converted these results to a thermal rate coefficient for forming either OH+ or H2O+, thereby accounting for the temperature dependence of the O fine-structure levels. Our results are in good agreement with two independent flowing afterglow measurements at a temperature of ≈ 300 K, and with a corresponding level of H3+ internal excitation. This good agreement strongly suggests that the internal excitation of the H3+ does not play a significant role in this reaction. The Langevin rate coefficient is in reasonable agreement with the experimental results at 10 K but a factor of ≈ 2 larger at 300 K. The two published classical trajectory studies using quantum mechanical potential energy surfaces lie a factor of ≈ 1.5 above our experimental results over this 10-300 K range.

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