Oxygen ion is one of the most important and special ions in the lower ionosphere, and it has been extensively studying. The First Negative band system (b4∑g-- a4âˆu) often happens in the ionization processes of oxygen molecules and in the chemical reaction intermediates of oxidation. However, the first negative system is a quartet transition and 48 branches are involved, which makes the assignment extraordinarily difficult.In this paper, the laser source was a single-mode Ti: sapphire laser (Coherent Ring 899-29) pumped by a compact diode-laser-pumped Nd:YVO4 laser (Coherent Verdi 10,at 532 nm). The O2+ ion was produced by the ac Penning discharge with high voltage in flowing gases of oxygen and helium. About 200 spectral lines in the region of 13170-13500 cm-1 belonging to 33 branches of the (2,6) band in the O2+ b4∑g-- a4âˆu transition were observed for the first time to our knowledge using optical heterodyne velocity modulation spectroscopy. A rotational analysis was performed, thus, more precise molecular constants of the both states involved were obtained employing nonlinear least-squares procedure via diagnalizing the effective Hamiltonian matrices.Furthermore, the RKR potential curves of both the a and b quartet states of O2+ were derived based on the latest equilibrium constants and Franck-Condon factors were listed in this thesis as well.
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