Quantum study of the N+N2 exchange reaction: State-to-state reaction probabilities, initial state selected probabilities, Feshbach resonances, and product distributions
Authors:
- 1 April 2004
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 120 (13) , 6041-6050
Abstract
We report a detailed three-dimensional time-dependent quantum dynamics study of the state-to-state N + N 2 exchange scattering in the 2.1–3.2 eV range using a recently developed ab initiopotential energy surface (PES). The reactive flux arrives at the dividing surface in the asymptotic product region in a series of six packets, instead of a single packet. Further study shows that these features arise from the “Lake Eyring” region of the PES, a region with a shallow well between two transition states. Trappings due to Feshbach resonances are found to be the major cause of the time delay. A detailed analysis of the Feshbach resonance features is carried out using an L 2 calculation of the metastable states in the “Lake Eyring” region. Strong resonance features are found in the state-to-state and initial state selected reaction probabilities. The metastable states with bending motions and/or bending coupled with stretching motions are found to be the predominant source of the resonance structure. Initial state selected reaction probabilities further indicate that the lifetimes of the metastable states with bending motions in the “Lake Eyring” region are longer than those of states with stretching motions and thus dominate the reactive resonances. Resonance structures are also visible in some of the integral cross sections and should provide a means for future experimental observation of the resonance behavior. A study of the final rotational distributions shows that, for the energy range studied here, the final products are distributed toward high-rotational states. Final vibrational distributions at the temperatures 2000 and 10 000 K are also reported.Keywords
This publication has 30 references indexed in Scilit:
- Forward scattering due to slow-down of the intermediate in the H + HD → D + H2 reactionNature, 2002
- Observation and interpretation of a time-delayed mechanism in the hydrogen exchange reactionNature, 2002
- Quantum mechanical and semiclassical studies of N+N2 collisions and their application to thermalization of fast N atomsThe Journal of Chemical Physics, 1998
- Quantum reactive scattering with a deep well: Time-dependent calculation for H+O2 reaction and bound state characterization for HO2The Journal of Chemical Physics, 1994
- Full-dimensional time-dependent treatment for diatom–diatom reactions: The H2+OH reactionThe Journal of Chemical Physics, 1994
- Temperature dependence of nitrogen atom-molecule rate coefficientsThe Journal of Physical Chemistry, 1994
- Quantum mechanical close coupling approach to molecular collisions. jz -conserving coupled states approximationThe Journal of Chemical Physics, 1974
- Space-fixed vs body-fixed axes in atom-diatomic molecule scattering. Sudden approximationsThe Journal of Chemical Physics, 1974
- Role of direct and resonant (compound state) processes and of their interferences in the quantum dynamics of the collinear H + H2 exchange reactionThe Journal of Chemical Physics, 1973
- Potential Energy Surface for H3The Journal of Chemical Physics, 1964