Journal
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 13, Issue 42, Pages 19148-19155Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cp21982k
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Funding
- Department of Energy, Office of Basic Energy Sciences
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We report theoretical results for reaction and vibrational quenching of the ultracold collision D + H-2 (nu, j = 0) for a wide range of initial vibrationally excited states nu. The nu-dependence of the zero-temperature limit of the reaction rate coefficient shows two distinct regimes: a barrier dominated regime for 0 <= nu <= 4, and a barrierless regime for nu >= 5. We also present detailed distributions over the rovibrational states of the products. We find an approximate conservation of the internal vibrational energy; namely, the branching ratios always favor the highly excited final states, which have vibrational energies similar to that of the entrance channel.
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