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Updated: Apr 29, 2026

Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Carbon dioxide ion dissociations after inner shell excitation and ionization: the origin of site-specific effects
J H D Eland1, S Zagorodskikh2, R J Squibb2
1Department of Chemistry, Physical and Theoretical Chemistry Laboratory, Oxford University, South Parks Road, Oxford OX1 3QZ, United Kingdom.
Abstract:
Multi-coincidence experiments with detection of both electrons and ions from decay of core-excited and core-ionized states of CO2 confirm that O2(+) is formed specifically in Auger decay from the C1s-π* and O1s-π* resonances. Molecular rearrangement occurs by bending in the resonant states, and O2(+) is produced by both single and double Auger decay. It is suggested that electron capture by C(+) after partial dissociation in the doubly ionized core of excited CO2(+), formed by shake-up in spectator resonant Auger decay, accounts for high kinetic energy and high internal energy in some C + O2(+) fragments.
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