中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Dissociation of polyatomic molecules in the intense femtosecond laser field

文献类型:期刊论文

作者Wang, C; Kong, FA
刊名ACTA PHYSICO-CHIMICA SINICA
出版日期2004-08-01
卷号20页码:1055-1062
关键词Intense Femtosecond Laser Field Tof-ms Field-assisted Dissociation Methane Acetone
ISSN号1000-6818
DOI10.3866/PKU.WHXB200408zk24
英文摘要Chemistry in strong laser fields is a new research field in which dissociation of molecules in the intense laser field is a current topic of interest. Our results, including the theoretical model of field-assisted dissociation (FAD) and the experimental investigations on the dissociation of CH4 and CH3COCH3 in the intense femtosecond laser field are presented. Some assumptions are made in the model. When a laser field applies to a molecule, only the change of the one bond length, which lies along with the laser field, is taken into account and the rest of the molecular geometry is fixed. In addition, only molecular ions in the ground electronic state are considered. Ab initio potential energy surfaces in the external fields indicate that chemical bond tends to dissociate. QCT (quasi-classical trajectory) calculations clearly show the processes of bond breaking. It was found that the calculations based on the theoretical model are in excellent agreement with the experiment data.
语种英语
WOS记录号WOS:000223283100024
出版者PEKING UNIV PRESS
源URL[http://ir.iccas.ac.cn/handle/121111/82107]  
专题中国科学院化学研究所
通讯作者Kong, FA
作者单位Chinese Acad Sci, Inst Chem, StateKey Lab Mol React Dynam, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Wang, C,Kong, FA. Dissociation of polyatomic molecules in the intense femtosecond laser field[J]. ACTA PHYSICO-CHIMICA SINICA,2004,20:1055-1062.
APA Wang, C,&Kong, FA.(2004).Dissociation of polyatomic molecules in the intense femtosecond laser field.ACTA PHYSICO-CHIMICA SINICA,20,1055-1062.
MLA Wang, C,et al."Dissociation of polyatomic molecules in the intense femtosecond laser field".ACTA PHYSICO-CHIMICA SINICA 20(2004):1055-1062.

入库方式: OAI收割

来源:化学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。