Two-photon photodissociation dynamics study of CS2: The S(1S) atom channel

Two-photon photodissociation dynamics of carbon disulfide (CS2) were studied by means of the sliced velocity map ion imaging technique. The S(1S) + CS(X1Σ+) channel was directly observed from the measured images of S(1S) products in the wavelength range of 290.10-336.88 nm. The translational energy distributions and angular distributions of fragments have been derived. Rovibrational states of the CS(X1Σ+) co-products were partially resolved in the translational energy spectra and can be populated up to the energy limit of the available energy. Experimental results also show that the product anisotropy parameters are β2 > 0 and β4 ∼ 0. The latter indicates that the intermediate state reached by the first one photon excitation has a quite long lifetime, while the former suggests the molecules undergo a parallel transition from the intermediate state to the final state upon the second photon excitation and then experience a fast dissociation process. Combined with previous studies, we propose a possible dissociation mechanism: after absorbing two photons in the range of 290.10-336.88 nm, the CS2 molecule may undergo a sequential transition 1A1(1Σg+) ← 11B2(1Δu)/1A2(1Δu) ← X1Σg+, then directly dissociate or couple to other electronic states and dissociate.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-07-24
DOI
https://doi.org/10.1063/5.0283135
Citations
1
Primary Topic
Mass Spectrometry Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.76

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article

Two-photon photodissociation dynamics study of CS2: The S(1S) atom channel

Yongxin Dong, Hua Wei, Quan Shuai, Xingan Wang et al.
1 citations
The Journal of Chemical Physics
Mass Spectrometry Techniques and Applications
0.76
article

Two-photon photodissociation dynamics study of CS2: The S(1S) atom channel

Yongxin Dong, Hua Wei, Quan Shuai, Xingan Wang, Shuaikang Yang, Kaijun Yuan, Zhiguo Zhang, Zhenxing Li, Xueming Yang, Zijie Luo
article en
1 citations

Abstract

Two-photon photodissociation dynamics of carbon disulfide (CS2) were studied by means of the sliced velocity map ion imaging technique. The S(1S) + CS(X1Σ+) channel was directly observed from the measured images of S(1S) products in the wavelength range of 290.10-336.88 nm. The translational energy distributions and angular distributions of fragments have been derived. Rovibrational states of the CS(X1Σ+) co-products were partially resolved in the translational energy spectra and can be populated up to the energy limit of the available energy. Experimental results also show that the product anisotropy parameters are β2 > 0 and β4 ∼ 0. The latter indicates that the intermediate state reached by the first one photon excitation has a quite long lifetime, while the former suggests the molecules undergo a parallel transition from the intermediate state to the final state upon the second photon excitation and then experience a fast dissociation process. Combined with previous studies, we propose a possible dissociation mechanism: after absorbing two photons in the range of 290.10-336.88 nm, the CS2 molecule may undergo a sequential transition 1A1(1Σg+) ← 11B2(1Δu)/1A2(1Δu) ← X1Σg+, then directly dissociate or couple to other electronic states and dissociate.

The Journal of Chemical PhysicsVol. 163(4)
University of Science and Technology of China (CN), Fuyang Normal University (CN), Anhui University (CN), Hefei University of Technology (CN), Dalian Institute of Chemical Physics (CN), Southern University of Science and Technology (CN), Hefei University (CN), Horological Research Institute of Light Industry (CN)
National Natural Science Foundation of China, Liaoning Revitalization Talents Program, Science and Technology Planning Project of Guangdong Province
Affordable and clean energy
Openalex Percentile: Top 28%
Mass Spectrometry Techniques and Applications
0.76
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