Journal
JOURNAL OF CHEMICAL PHYSICS
Volume 150, Issue 22, Pages -Publisher
AMER INST PHYSICS
DOI: 10.1063/1.5096236
Keywords
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Funding
- NSFC [21773221, 21727804]
- MOST-NKRDP [2017YFA0303502]
- Fundamental Research Funds for the Central Universities of China [WK2340000078]
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Photodissociation dynamics of the N2O+ cation in its B-2 state has been experimentally studied in an energy region around the NO+((1)sigma(+)) + N(P-2) dissociation limit using a cryogenic cylindrical ion trap velocity map imaging spectrometer. The results show that the NO+((1)sigma(+)) + N(D-2) product channel dominates the dissociation dynamics and requires the NNO angle to change by 30 degrees-50 degrees prior to dissociation. The NO+((1)sigma(+)) + N(P-2) product channel, which directly correlates with the B-2 state but less competitive, opens immediately when the photon energy reaches the dissociation limits, indicating a flat dissociation pathway without bending on the B-2 state surface.
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