题名 | Vacuum ultraviolet photodissociation dynamics of OCS via the F Rydberg state: The S(3PJ = 2, 1, 0) product channels |
作者 | |
通讯作者 | Wang,Xingan |
发表日期 | 2022-04-01
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DOI | |
发表期刊 | |
ISSN | 1674-0068
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EISSN | 2327-2244
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卷号 | 35期号:2页码:249-256 |
摘要 | Vacuum ultraviolet (VUV) photodissociation dynamics of carbonyl sulfide was investigated experimentally by using a tunable photolysis light source and the time-sliced velocity map ion imaging technique. Ion images of S(3PJ =2, 1, 0) dissociation products were measured at five photolysis wavelengths from 133.26 nm to 139.96 nm, corresponding to the F Rydberg state of OCS. Two dissociation channels: S(3PJ)+CO(X1ς+) and S(3PJ)+CO(A3Π) were observed with the former being dominant. The vibrational states of CO co-products were partially resolved in the ion images. The product total kinetic energy releases, anisotropy parameters (β), and the branching ratios of high-lying CO vibrational states were determined for the S(3PJ)+CO(X1ς+) channel. We found that the anisotropy parameters suddenly changed from negative to positive when OCS was excited to the higher vibrational levels of the F state. Furthermore, the anisotropy parameters for S(3PJ) products of J = 2, 1, 0 were even different. These anomalous phenomena may result from the simultaneous existence of both parallel and perpendicular dissociation mechanisms, suggesting the involvement of other electronic states with different symmetry in the initially-excited energy region. This work provides a further understanding of the nonadiabatic couplings in the VUV photodissociation process of OCS. |
关键词 | |
相关链接 | [Scopus记录] |
收录类别 | |
语种 | 英语
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学校署名 | 其他
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资助项目 | National Key R&D Program of China[2016YFF0200500]
; National Natural Science Foundation of China[22125302]
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WOS研究方向 | Physics
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WOS类目 | Physics, Atomic, Molecular & Chemical
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WOS记录号 | WOS:000820672900001
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出版者 | |
EI入藏号 | 20222012107757
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EI主题词 | Anisotropy
; Excited states
; Ions
; Kinetic energy
; Kinetics
; Light sources
; Photolysis
; Sulfur compounds
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EI分类号 | Fluid Flow, General:631.1
; Physical Chemistry:801.4
; Chemical Reactions:802.2
; Classical Physics; Quantum Theory; Relativity:931
; Physical Properties of Gases, Liquids and Solids:931.2
; Atomic and Molecular Physics:931.3
; Quantum Theory; Quantum Mechanics:931.4
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Scopus记录号 | 2-s2.0-85129839929
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来源库 | Scopus
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引用统计 |
被引频次[WOS]:4
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成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/334825 |
专题 | 南方科技大学 |
作者单位 | 1.Department of Chemical Physics,University of Science and Technology of China,Hefei,230026,China 2.Hangzhou Institute of Advanced Studies,Zhejiang Normal University,Hangzhou,311231,China 3.State Key Laboratory of Molecular Reaction Dynamics,Dalian Institute of Chemical Physics,Chinese Academy of Sciences,Dalian,116023,China 4.School of Science,Southern University of Science and Technology,Shenzhen,518055,China |
推荐引用方式 GB/T 7714 |
Tang,Ling,Chen,Wentao,Yuan,Daofu,et al. Vacuum ultraviolet photodissociation dynamics of OCS via the F Rydberg state: The S(3PJ = 2, 1, 0) product channels[J]. 化学物理学报,2022,35(2):249-256.
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APA |
Tang,Ling,Chen,Wentao,Yuan,Daofu,Yu,Shengrui,Yang,Xueming,&Wang,Xingan.(2022).Vacuum ultraviolet photodissociation dynamics of OCS via the F Rydberg state: The S(3PJ = 2, 1, 0) product channels.化学物理学报,35(2),249-256.
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MLA |
Tang,Ling,et al."Vacuum ultraviolet photodissociation dynamics of OCS via the F Rydberg state: The S(3PJ = 2, 1, 0) product channels".化学物理学报 35.2(2022):249-256.
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条目包含的文件 | 条目无相关文件。 |
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