Coulomb explosion and dissociative ionization of 1,2-dibromoethane under an intense femtosecond laser field

被引:8
|
作者
Wu, Hua [1 ]
Zhang, Shian [1 ]
Yang, Yan [1 ,2 ]
Sun, Shengzhi [1 ]
Zhang, Jian [1 ]
Deng, Li [1 ]
Jia, Tianqing [1 ]
Wang, Zugeng [1 ]
Sun, Zhenrong [1 ]
机构
[1] E China Normal Univ, Dept Phys, State Key Lab Precis Spect, Shanghai 200062, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Opt & Fine Mech, State Key Lab High Field Laser Phys, Shanghai 201800, Peoples R China
来源
RSC ADVANCES | 2014年 / 4卷 / 85期
关键词
DOWN ABSORPTION-SPECTROSCOPY; CONCERTED 3-BODY FORMATION; BR BOND FISSION; ULTRAVIOLET PHOTODISSOCIATION; ATMOSPHERIC BROMINE; MOLECULAR-OXYGEN; 1ST CONTINUUM; 248; NM; ION; ELIMINATION;
D O I
10.1039/c4ra06121g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Coulomb explosion and dissociative ionization of 1,2-dibromoethane are experimentally investigated in a near-infrared (800 nm) femtosecond laser field by dc-slice imaging technology. The sliced images of the fragment ions C2H4Br+, Br+, C2H4+, Br-2(+) and CH2Br+ are obtained, and their corresponding kinetic energy releases (KERs) and angular distributions are calculated. It is confirmed that the high-KER components come from Coulomb explosion of 1,2-C2H4Br22+, while the low-KER components come from dissociative ionization of 1,2-C2H4Br2+. Furthermore, the dissociation pathway leading to C2H4+ and Br-2 is theoretically simulated, and the results show that the singly charged precursor overcomes an energy barrier to dissociate via an asynchronous concerted mechanism after undergoing isomerization.
引用
收藏
页码:45300 / 45305
页数:6
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