A full-dimensional quantum dynamics study of the mode specificity in the H + HOD abstraction reaction
We employ the initial state-selected time-dependent wave packet approach to an atom-triatom reaction to study the H + HOD → OH + HD/OD + H{sub 2} reaction without the centrifugal sudden approximation, based on an accurate potential energy surface which was recently developed by neural network fitting to high level ab initio energy points. The total reaction probabilities and integral cross sections, which are the exact coupled-channel results, are calculated for the HOD reactant initially in the ground and several vibrationally excited states, including the bending excited state, OD stretching excited states, OH stretching excited states, and combined excitations of them. The reactivity enhancements from different initial states of HOD are presented, which feature strong bond-selective effects of the reaction dynamics. The current results for the product branching ratios, reactivity enhancements, and relative cross sections are largely improved over the previous calculations, in quantitatively good agreement with experiment. The thermal rate constant for the title reaction and the contributions from individual vibrational states of HOD are also obtained.
- OSTI ID:
- 22416115
- Journal Information:
- Journal of Chemical Physics, Vol. 142, Issue 6; Other Information: (c) 2015 AIP Publishing LLC; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
GENERAL PHYSICS
ATOMS
BRANCHING RATIO
COUPLED CHANNEL THEORY
EXCITATION
HEAVY WATER
HYDROGEN
INTEGRAL CROSS SECTIONS
NEURAL NETWORKS
POTENTIAL ENERGY
PROBABILITY
REACTION KINETICS
REACTIVITY
SPECIFICITY
SUDDEN APPROXIMATION
TIME DEPENDENCE
VIBRATIONAL STATES
WAVE PACKETS