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Differential Cross Sections and Collision-Induced Rotational Alignment in Inelastic Scattering of NO(X) by Xe
Authors:Mark Brouard  Helen Chadwick  Sean DS Gordon  Cornelia G Heid  Balazs Hornung  Bethan Nichols  Jacek K?os  Pablo G Jambrina  FJavier Aoiz
Institution:a.The Department of Chemistry, University of Oxford, The Chemistry Research Laboratory, 12 Mansfield Road, Oxford OX1 3TA, UKb.Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, USAc.Departamento de Química Física, Facultad de Ciencias Químicas, University of Salamanca, Salamanca, Spaind.Departamento de Química Física, Facultad de Química, Universidad Complutense, 28040 Madrid, Spain
Abstract:Fully \begin{document}$ \Lambda $\end{document}-doublet resolved differential cross sections and collision-induced rotational alignment moments have been measured for the NO(X)–Xe collision system at a collision energy of 519 cm\begin{document}$ ^{-1} $\end{document}. The experiments combine initial quantum state selection, employing a hexapole inhomogeneous electric field, with quantum state resolved detection, using (1+1\begin{document}$ ' $\end{document}) resonantly enhanced multiphoton ionization and velocity map ion imaging. The differential cross sections and polarization dependent differential cross sections are shown to agree well with quantum mechanical scattering calculations performed on ab initio potential energy surfaces J. K?os et al. J. Chem. Phys. 137 , 014312 (2012)]. By comparison with quasi-classical trajectory calculations, quantum mechanical scattering calculations on a hard-shell potential, and kinematic apse model calculations, the effects of the attractive part of the potential on the measured differential cross sections and collision-induced rotational alignment moments are assessed.
Keywords:Chemical Physics  Reaction dynamics  Inelastic scattering
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