Tracking Intramolecular Vibrational Redistribution in Polyatomic Small-Molecule Liquids by Ultrafast Time-Frequency-Resolved CARS

被引:18
|
作者
Liu, Xiaosong [1 ]
Zhang, Wei [1 ]
Song, Yunfei [3 ]
Yu, Guoyang [3 ]
Zheng, Zhaoyang [3 ]
Zeng, Yangyang [3 ]
Lv, Zhe [1 ]
Song, Huajie [2 ]
Yang, Yanqiang [1 ,3 ]
机构
[1] Harbin Inst Technol, Dept Phys, Harbin 150001, Peoples R China
[2] Beijing Inst Appl Phys & Computat Math, Beijing 100088, Peoples R China
[3] China Acad Engn Phys, Inst Fluid Phys, Natl Key Lab Shock Wave & Detonat Phys, Mianyang 622150, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2017年 / 121卷 / 26期
基金
中国国家自然科学基金;
关键词
CH STRETCHING VIBRATIONS; ENERGY-FLOW; BENZENE MOLECULES; DYNAMICS; RELAXATION; LEVEL; DIMER;
D O I
10.1021/acs.jpca.7b05578
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Selective excitation of C-H stretching vibrational modes, detection of intramolecular vibrational energy redistribution (IVR), and vibrational modes coupling in the electronic ground state of benzene are performed by using femtosecond time- and frequency-resolved coherent anti-Stokes Raman scattering (CARS) spectroscopy. Both of the parent modes in the Raman-active bands are coherently excited by an ultrafast stimulated Raman pump, giving initial excitations of 3056 cm(-1) (A(1g)) and 3074 cm(-1) (E-2g) and subsequent IVR from the parent modes to daughter modes of 1181 and 992 cm(-1), and the coherent vibrational coupling of the relevant modes is tracked. The directionality and selectivity of IVR and coherent coupling among all of the relevant vibrational modes are discussed in the view of molecular symmetry.
引用
收藏
页码:4948 / 4952
页数:5
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