Imaging characterization of the rapid adiabatic passage in a source-rotatable, crossed-beam scattering experiment

被引:9
|
作者
Pan, Huilin [1 ]
Mondal, Sohidul [1 ]
Yang, Chung-Hsin [1 ]
Liu, Kopin [1 ,2 ]
机构
[1] Acad Sinica, Inst Atom & Mol Sci, POB 23-166, Taipei 10617, Taiwan
[2] Natl Taiwan Univ, Dept Phys, Taipei 10617, Taiwan
来源
JOURNAL OF CHEMICAL PHYSICS | 2017年 / 147卷 / 01期
关键词
VIBRATIONALLY EXCITED METHANE; GAS-SURFACE REACTION; FREQUENCY STABILIZATION; STRETCHING EXCITATION; BIMOLECULAR REACTIONS; RELATIVE REACTIVITY; CHLORINE ATOM; SPECTROSCOPY; CL; DYNAMICS;
D O I
10.1063/1.4982615
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
In order to achieve a more efficient preparation of a specific ro-vibrationally excited reactant state for reactive scattering experiments, we implemented the rapid adiabatic passage ( RAP) scheme to our pulsed crossed-beam machine, using a single-mode, continuous-wave mid-infrared laser. The challenge for this source-rotatable apparatus lies in the non-orthogonal geometry between the molecular beam and the laser propagation directions. As such, the velocity spread of the supersonic beam results in a significantly broader Doppler distribution that needs to be activated for RAP to occur than the conventional orthogonal configuration. In this report, we detail our approach to shifting, locking, and stabilizing the absolute mid-infrared frequency. We exploited the imaging detection technique to characterize the RAP process and to quantify the excitation efficiency. We showed that with appropriate focusing of the IR laser, a nearly complete population transfer can still be achieved in favorable cases. Compared to our previous setup-a pulsed optical parametric oscillator/amplifier in combination with a multipass ring reflector for saturated absorption, the present RAP scheme with a single-pass, continuous-wave laser yields noticeably higher population-transfer efficiency. Published by AIP Publishing.
引用
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页数:10
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