Full-dimensional automated potential energy surface development and detailed dynamics for the CH<sub>2</sub>OO + NH<sub>3</sub> reaction
With the help of the ROBOSURFER program package, a global full-dimensional potential energy surface (PES) for the reaction of the Criegee intermediate, CH2OO, with the NH3 molecule is developed iteratively using different ab initio methods and the monomial symmetrization fitting approach. The final...
Elmentve itt :
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| Dokumentumtípus: | Cikk |
| Megjelent: |
2023
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| Sorozat: | PHYSICAL CHEMISTRY CHEMICAL PHYSICS
25 No. 39 |
| Tárgyszavak: | |
| doi: | 10.1039/d3cp03469k |
| mtmt: | 34337803 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/31845 |
| Tartalmi kivonat: | With the help of the ROBOSURFER program package, a global full-dimensional potential energy surface (PES) for the reaction of the Criegee intermediate, CH2OO, with the NH3 molecule is developed iteratively using different ab initio methods and the monomial symmetrization fitting approach. The final permutationally-invariant analytical PES is constructed based on 23447 geometries and the corresponding ManyHF-based CCSD(T)-F12b/cc-pVTZ-F12 energies. The accuracy of the PES is confirmed by the excellent agreement of its stationary-point properties and one-dimensional potential energy curves compared with the corresponding ab initio data. The reaction probabilities and integral cross sections are calculated for the ground-state and several vibrationally excited-state reactions by quasi-classical trajectory simulations. Remarkable is that the maximum impact parameter b where reactivity vanishes is almost independent of collision energy ranging from 1 to 40 kcal mol(-1), and the reaction probability increases with increasing collision energy for this negative-barrier reaction. At the same time, a slight mode-specificity effect is observed. In addition, the deuterium effect is investigated and the sudden vector projection is discussed. |
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| Terjedelem/Fizikai jellemzők: | 26917-26922 |
| ISSN: | 1463-9076 |