State- and orientation-dependent N2 emission in the N2O+Cs reaction

被引:16
作者
Brandt, M [1 ]
Greber, T
Kuhlmann, F
Bowering, N
Heinzmann, U
机构
[1] Univ Bielefeld, Fak Phys D4, D-33501 Bielefeld, Germany
[2] Univ Zurich, Inst Phys, CH-8057 Zurich, Switzerland
关键词
alkali metals; molecular dynamics; molecule-solid reactions; nitrogen oxides; oxidation; surface chemical reaction;
D O I
10.1016/S0039-6028(97)00954-0
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 interaction of state-selected and oriented N2O molecules in the first excited n(2) = l bending mode with one monolayer of Cs on Pt(111) is studied by means of time-of-flight mass spectroscopy in a molecular beam experiment. State-selected and oriented N2O molecules were prepared using electrostatic hexapole and dipole fields. The emission of N-2 molecules induced by the abstraction reaction (N2O + Cs --> CsO + N-2) depends strongly on the molecular state and its orientation. Direct abstraction and backscattering of N-2 molecules is observed for N2O ground-state molecules in the n(2) = 1 first vibrationally excited bending mode. A distinct steric effect has been found for N-2 molecules emitted specularly with respect to the incoming N2O molecules. These findings are explained in a picture where direct N-2 emission is triggered by resonant N2O ionization (harpooning). The results are discussed in the context of recent exoelectron emission experiments. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:160 / 164
页数:5
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