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- W2329446970 abstract "The vacuum ultraviolet (VUV) pulsed field ionization–photoelectron (PFI–PE) spectra for CO2 have been measured in the energy range of 17.2–19.0 eV, showing complex vibronic structures for the CO2+(A 2Πu and B 2Σu+) states. The PFI–PE spectra for CO2+(A 2Πu and B 2Σu+) are dominated by the v1+ (symmetric stretching) vibrational progressions, and weak bands due to excitation of both even and odd quanta of the v2+ (bending) and v3+ (antisymmetric stretching) modes are observed in the VUV–PFI–PE spectra. The simulation of rotational contours resolved in the PFI–PE vibronic bands associated with excitation to CO2+(A 2Π3/2,1/2u;v1+=0–5,v2+=0,v3+=0) and CO2+(B 2Σu+;0,0,0) has yielded accurate ionization energies for the formation of these states from CO2(X 1Σg+). Three-dimensional potential energy functions (PEFs) for CO2+(B 2Σu+) have also been generated theoretically using the complete active space self-consistent field and internally contracted multireference configuration interaction methods. Based on these PEFs, vibrational energy levels for CO2+(B 2Σu+), together with the Franck–Condon factors for their formation from CO2(X 1Σg+), have been calculated. With the guide of these theoretical predictions, the vibrational bands resolved in the PFI–PE spectrum for CO2+(B 2Σu+) have been satisfactorily assigned. This assignment reveals the nature of many vibrational PFI–PE bands as originated from anharmonic resonance interactions and members of Fermi polyads." @default.
- W2329446970 created "2016-06-24" @default.
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- W2329446970 date "2000-11-08" @default.
- W2329446970 modified "2023-09-23" @default.
- W2329446970 title "Pulsed field ionization–photoelectron bands for CO2+(A 2Πu and B 2Σu+) in the energy range of 17.2–19.0 eV: An experimental and theoretical study" @default.
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- W2329446970 doi "https://doi.org/10.1063/1.1314354" @default.
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