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Title: Photoelectron imaging and photodissociation of ozonide in O{sub 3}{sup −} ⋅ (O{sub 2}){sub n} (n = 1-4) clusters

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4916048· OSTI ID:22415562

The photoelectron images of O{sub 3}{sup −} and O{sub 3}{sup −} ⋅ (O{sub 2}){sub n} (n = 1–4) have been measured using 3.49 eV photon energy. The spectra exhibit several processes, including direct photodetachment and photodissociation with photodetachment of O{sup −} photofragments. Several spectra also exhibit autodetachment of vibrationally excited O{sub 2}{sup −} photofragments. Comparison of the bare O{sub 3}{sup −} photoelectron spectra to that of the complexes shows that the O{sub 3}{sup −} core is preserved upon clustering with several O{sub 2} molecules, though subtle changes in the Franck-Condon profile of the ground state photodetachment transition suggest some charge transfer from O{sub 3}{sup −} to the O{sub 2} molecules. The electron affinities of the complexes increase by less than 0.1 eV with each additional O{sub 2} molecule, which is comparable to the corresponding binding energy [K. Hiraoka, Chem. Phys. 125, 439-444 (1988)]. The relative intensity of the photofragment O{sup −} detachment signal to the O{sub 3}{sup −} ⋅ (O{sub 2}){sub n} direct detachment signal increases with cluster size. O{sub 2}{sup −} autodetachment signal is only observed in the O{sub 3}{sup −}, O{sub 3}{sup −} ⋅ (O{sub 2}){sub 3}, and O{sub 3}{sup −} ⋅ (O{sub 2}){sub 4} spectra, suggesting that the energy of the dissociative state also varies with the number of O{sub 2} molecules present in the cluster.

OSTI ID:
22415562
Journal Information:
Journal of Chemical Physics, Vol. 142, Issue 12; 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