摘要
The multi-photon dissociation and Coulomb explosion of ethyl bromide C2H5Br under near-infrared (800 nm) femtosecond laser field are experimentally investigated by a DC-sliced ion imaging technique. The sliced images of fragment ions C2H5+, Br+, CH3+, CH2Br+, H2+ and C2H3Br+ are obtained, and their dissociative pathways are assigned by observing their corresponding kinetic energy release (KER) and angular distribution. It is shown that low-KER components of these fragment ions result from multi-photon dissociation of singly charged parent ion C2H5Br+, while high-KER components come from Coulomb explosion of doubly charged parent ion C2H5Br2+. It is also shown that the precursor species [C2H5+...Br+] has a longer lifetime than [C2H3Br+...H2+] and [CH3...CH2Br+]. In addition, the probable H2 and H2+ elimination channels are theoretically simulated by Gaussian 09 software packages, and the results show that the former is an asynchronous process while the latter is a synchronous process.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 37078-37084 |
| 页数 | 7 |
| 期刊 | RSC Advances |
| 卷 | 5 |
| 期 | 46 |
| DOI | |
| 出版状态 | 已出版 - 2015 |
指纹
探究 'Dissociative ionization and Coulomb explosion of ethyl bromide under a near-infrared intense femtosecond laser field' 的科研主题。它们共同构成独一无二的指纹。引用此
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