State-to-state inelastic scattering of Stark-decelerated OH radicals with Ar atoms

被引:55
作者
Scharfenberg, Ludwig [1 ]
Klos, Jacek [2 ]
Dagdigian, Paul J. [3 ]
Alexander, Millard H. [2 ,4 ]
Meijer, Gerard [1 ]
van de Meerakker, Sebastiaan Y. T. [1 ]
机构
[1] Fritz Haber Inst Max Planck Gesell, D-14195 Berlin, Germany
[2] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
[3] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
[4] Univ Maryland, Inst Phys Sci & Technol, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
DIFFERENTIAL CROSS-SECTIONS; LASER-INDUCED FLUORESCENCE; POTENTIAL-ENERGY SURFACE; MOLECULAR-BEAMS; WAVE-FUNCTIONS; VIBRATIONAL-EXCITATION; BIMOLECULAR REACTIONS; BASIS-SETS; COLLISIONS; SPECTROSCOPY;
D O I
10.1039/c004422a
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
The Stark deceleration method exploits the concepts of charged particle accelerator physics to produce molecular beams with a tunable velocity. These tamed molecular beams offer interesting perspectives for precise crossed beam scattering studies as a function of the collision energy. The method has advanced sufficiently to compete with state-of-the-art beam methods that are used for scattering studies throughout. This is demonstrated here for the scattering of OH radicals (X-2 Pi(3/2), J = 3/2, f) with Ar atoms, a benchmark system for the scattering of open-shell molecules with atoms. Parity-resolved integral state-to-state inelastic scattering cross sections are measured at collision energies between 80 and 800 cm(-1). The threshold behavior and collision energy dependence of 13 inelastic scattering channels is accurately determined. Excellent agreement is obtained with the cross sections predicted by close-coupling scattering calculations based on the most accurate ab initio OH + Ar potential energy surfaces to date.
引用
收藏
页码:10660 / 10670
页数:11
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