Abstract
Electronic states of the O 2 + ion are evaluated by diagonalization of the exact effective valence shall Hamiltonian H v which has been previously calculated for O 2. The present calculations are then essentially complete valence shall configuration interaction calculations using the same orbitals as for the O 2 calculation, but including correlation contributions from all single and double excitations out of the valence shell. The computed results demonstrate the transferability of the H v of O 2 to the O 2 + system.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
