Laser-induced fluorescence spectroscopic study of the [21.2]0+-X0+ and [22.2]0+-X0+ electronic transitions of tungsten monoxide

被引:9
|
作者
Zhang, Jicai [1 ,2 ]
Zhao, Dongmei [1 ]
Xiang, Qianlan [3 ]
Ma, Xinwen [1 ]
Yang, Jie [1 ]
机构
[1] Chinese Acad Sci, Inst Modern Phys, Lanzhou 730000, Gansu, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Xianyang Normal Univ, Xianyang 712000, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
WO; Laser-induced fluorescence (LIF); Isotopic shift; ABSORPTION-SPECTRA; WO MOLECULES; OXIDES; MOO;
D O I
10.1016/j.jms.2018.12.001
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
The laser-induced fluorescence (LIF) excitation spectra of jet-cooled WO molecule have been investigated in the range of 21,000-23,200 cm(-1) , and two electronic band systems have been observed for the first time and labeled as the [21.2]0(+)-X0(+) and [22.2]0(+)-X0(+) transitions. The vibrational and rotational constants of these two excited electronic states have been derived by rotational analysis of the spectra. The tungsten isotopic structures of these two excited states are clearly resolved, and the analysis of LIF spectra reveals that the isotopic shifts are due to the strong interstate perturbations between different vibronic states. Based on the ab initio calculation results by Ram et al., the primarily attributed configuration of these two newly identified states was discussed. In addition, the lifetimes of the observed vibronic states were measured under the collision-free condition. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:96 / 100
页数:5
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