Λ-type doublets and lifetime broadening in the B2Π-X2Π electronic origin band of C6H

被引:0
|
作者
Xiao, Zengjun
Gu, Jieqiong
Li, Zhenzhen
Chu, Wangyou
Zhang, Qiang
Chen, Yang [1 ]
Zhao, Dongfeng [1 ]
机构
[1] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Hefei 230026, Peoples R China
基金
国家重点研发计划;
关键词
C6H radical; Cavity ring-down spectroscopy; Lambda-type doubling; Lifetime broadening; LINEAR CARBON CHAINS; HYPERFINE-STRUCTURE; ABSORPTION-SPECTRA; NEON MATRICES; STATE; C5H; SPECTROSCOPY; MOLECULES; RADICALS; C3H;
D O I
10.1063/1674-0068/cjcp2304030
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
We present a high-resolution study on the B-2 Pi-X-2 Pi electronic origin band spectrum of the C6H radical with its center at similar to 18990 cm(-1) The C6H radicals are produced in a pulsed supersonic slit-jet discharge source and detected in direct absorption by sensitive cavity ring-down spectroscopy. By using a home-made narrow linewidth nanosecond pulsed laser source, the experimental spectrum allows to resolve the Lambda-type doublet fine structures in high-J rotational lines. A set of improved B-2 Pi state constants, including the Lambda-type doubling parameters of p ' = -1.16(9)x10(-3) cm(-1) q ' = -1.22(7)x10(-4) cm(-1) are determined from analysis of the experimental spectrum. An analysis on the spectral line profile has resulted in a significant linewidth broadening of similar to 0.05 +/- 0.01 cm(-1), corresponding to a B-2 Pi state lifetime of similar to 100 +/- 20 ps. The short lifetime of the excited B-2 Pi state is proposed due to fast internal vibronic couplings to high-lying vibronic levels of lower electronic states.
引用
收藏
页码:19 / 23
页数:5
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