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Photodissociation Dynamics of OCS Near 128 nm:S(3PJ=2,1,0),S(1D2)and S(1S0)Channels

OCS分子在128 nm附近的光解动力学研究:S(3PJ=2,1,0)、S(1D2)以及S(1S0)产物通道
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摘要 Here we report the study of the photodissociation dynamics of carbonyl sulfide in the vacuum ultraviolet region using the time-sliced velocity map ion imaging technique.Images of S(^3PJ=2,1,0),S(^1D2)and S(^1S0)products were measured at four photolysis wave-lengths of 129.32,128.14,126.99,and 126.08 nm,respectively.Four main dissociation channels:S(^3PJ=2,1,0)+CO(X^1Σ^+),S(^3PJ=2,1,0)+CO(A^3π),S(^1D2)+CO(X^1Σ^+)and S(^1S0)+CO(X^1Σ^+)channels,have been clearly observed and identified.Vibrational states of the CO co-products were partially resolved in the experimental images.From these images,the product total kinetic energy releases,the branching ratios and angular distributions of products have been derived.While the S(^3PJ=2,1,0)+CO(A^3π)product channel is formed through the adiabatic dissociation process after the excitation to the(3^1Σ^+)excited state,the results suggest that strong nonadiabatic coupling plays an important role in the formation of other three channels.
作者 Si-wen Wang Dao-fu Yuan Wen-tao Chen Ling Tang Sheng-rui Yu Xue-ming Yang Xing-an Wang 王思雯;袁道福;陈文韬;唐翎;俞盛锐;杨学明;王兴安(中国科学技术大学化学物理系,合肥微尺度物质科学国家研究中心,合肥230026;浙江师范大学杭州高等研究院,杭州311231;中国科学院大连化学物理研究所,分子反应动力学国家重点实验室,大连116023;南方科技大学理学院化学系,深圳518055)
出处 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2020年第2期167-172,I0002,共7页 化学物理学报(英文)
基金 supported by the National Key R&D Program of China (No.2016YFF0200500) the National Natural Science Foundation of China (No.21473173,No.21590802,No.21327901 and No.21773213) the Strategic Priority Research Program of Chinese Academy of Sciences (No.XDB17000000) the Fundamental Research Funds for the Central Universities.
关键词 Vacuum ultraviolet photodissociation Carbonyl sulfide Velocity map ion imaging 真空紫外光解 OCS 离子速度影像
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