Vibronic interaction in CO 3 - photo-detachment: Jahn-Teller effects beyond structural distortion and general formalisms for vibronic Hamiltonians in trigonal symmetries
Physical Chemistry Chemical Physics , Volume 21 - Issue 17 p. 8679- 8690
Recently, the negative ion photoelectron spectrum of CO 3 - was reported and the second lowest energy band is assigned to the close-lying 3 E′′ and 3 E′ states that undergo Jahn-Teller distortions (Chem. Sci., 2016, 7, 1142). This assignment is based on the Born-Oppenheimer approximation and the assumption of a static Jahn-Teller effect that distorts the CO 3 structure from D 3h to C 2v symmetry. In this work, we employ a 4 states 6 modes vibronic coupling model to investigate the triplet band and uncover the dynamic and non-adiabatic nature of the Jahn-Teller and pseudo-Jahn-Teller interactions in the triplet states. The apparent four peaks progression in the band is studied in depth, and is found to consist of more than four transitions. By comparing the simulated spectra using the full model and the reduced-dimension 2 states 2 modes models, we characterize those transitions. The origin of the complexities of the spectrum is traced to the C-O nonbonding character of the orbitals that lose electron in the photo-detachment process. Methodology-wise, we derive and present the formalisms for arbitrary order expansions of all bimodal trigonal Jahn-Teller and pseudo-Jahn-Teller Hamiltonians in vibrational coordinates.
|Physical Chemistry Chemical Physics|
|Organisation||Department of Chemistry|
Seidu, I. (Issaka), Goel, P. (Prateek), Wang, X.-G. (Xiao-Gang), Chen, B. (Bo), Wang, X.-B. (Xue-Bin), & Zeng, T. (2019). Vibronic interaction in CO 3 - photo-detachment: Jahn-Teller effects beyond structural distortion and general formalisms for vibronic Hamiltonians in trigonal symmetries. Physical Chemistry Chemical Physics, 21(17), 8679–8690. doi:10.1039/c9cp01352k