光解
离解(化学)
激发态
化学
激发
原子物理学
波长
分子
光化学
物理
光学
物理化学
量子力学
有机化学
作者
Zhenxing Li,Zhao Min,Ting Xie,Yao Chang,Zijie Luo,Zhichao Chen,Xingan Wang,Kaijun Yuan,Xueming Yang
出处
期刊:Molecular Physics
[Informa]
日期:2020-09-02
卷期号:119 (1-2): e1813911-e1813911
被引量:5
标识
DOI:10.1080/00268976.2020.1813911
摘要
Two-photon dissociation dynamics of carbon disulfide (CS2) have been studied by using the time-sliced velocity map ion imaging technique. Images of the S (1D2) and S (3P0) photoproducts formed in the CS2 photodissociation are acquired at four photolysis wavelengths from 303 nm to 315 nm. Vibrational states of the CS co-products are partially resolved and identified in the images. The CS (X1Σ+) products are highly vibrationally excited with moderate rotational excitation. The spin–orbit state-specific dissociation dynamics are also investigated by measuring the images of three S (3PJ) spin–orbit states (J=0, 1, and 2) at photolysis wavelength 303.878 nm. The branching ratios of CS (a3Φ)/CS (X1Σg+) are determined to be 0.05 ± 0.02, 0.17 ± 0.04, and 0.26 ± 0.05 for the three spin–orbit states S (3P0), S (3P1), and S (3P2) respectively, implying a strong spin–orbit coupling exists in the dissociation process. The averaged anisotropy parameters β2>0 and β4∼0 suggest that the CS2 molecules undergo a sequential transition 21B2(21Σ+)←11B2(1Δu)←X1Σg+ with the intermediate state 11B2 having a long lifetime, followed by nonadiabatic and spin–orbit couplings to other electronic states and then dissociate.
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