STATE-SELECTED VIBRATIONAL-RELAXATION RATES FOR HIGHLY VIBRATIONALLY EXCITED OXYGEN MOLECULES
The state-selected vibrational relaxation rates in O2+ O 2 collisions, with one O2 molecule in a highly vibrationally excited state, have been calculated from first principles. The vibrationally close-coupled, rotationally infinite order sudden approximation has been used to treat the collision dyna...
| Auteurs principaux: | , , |
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| Format: | Journal article |
| Publié: |
1995
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