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中国物理学会期刊

N2O+离子A2Σ+电子态的光谱研究

CSTR: 32037.14.aps.53.1027

The spectral assignment for the A2Σ+←X2Π transition of N2O+ ions

CSTR: 32037.14.aps.53.1027
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  • 用一束波长为360.55 nm的激光,通过N2O分子的(3+1)共振增强多光子电离过程制备纯净的母体离子N2O+ X2Π3/2,1/2(000).用另一束可调谐激光将N2O+离子激发至预解离态A2Σ+,利用飞行时间质谱检测解离碎片NO+离子强度随光解光波长的变化,在278—328 nm波长

     

    The spectra of N2O+ ions in A2Σ+ state have been investigated. Pure parent N2O+ ions, in the X2Π3/2,1/2(000) state, were prepared by (3+1) multiphoton ionization of jet-cooled N2O molecules using a laser beam at 360.55 nm. By introducing another laser, the parent ions were excited to the predissociative A2Σ+ state, and the fragment NO+ was detected by a time-of-flight mass spectrometer. The NO+ photofragment excitation (PHOFEX) spectra were recorded by scanning the dissociation laser in the wavelength range of 278—328 nm. The PHOFEX spectra could be attributed completely to the A2Σ+←X2Π transition of N2O+, in which most vibronic bands were observed for the first time. By considering the Fermi resonance between the ν1 and ν2 modes, the spectra were assigned, and the spectral constants, such as vibrational frequencies, anharmonic constants, and Fermi interaction constant, were obtained with relatively high reliability and precision.

     

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