Development of a Hyperthermal State-selected Molecular Oxygen Beam and Its Application to the Study of O 2 Adsorption on Pt(111)

M. Kurahashi, H. Ueta
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Abstract

A single spin-rotational state-selected [(J,M)=(2,2)] O2 beam allows us to conduct a spinand alignment -controlled O2 chemisorption experiment. We have recently expanded its available translational energy range to 0.10.9 eV. In this study, the beam has been used for the analysis of O2 chemisorption on Pt(111). Although this system has been investigated intensively due to its technological importance, the origin of the low O2 sticking probability and its unusual energy dependence has remained unclear. The present results indicate that, at low translational energy (E0) conditions, direct activated chemisorption occurs only when the O2 axis is nearly parallel to the surface. At high energy conditions (E0>0.5 eV), however, the sticking probability for the parallel O2 decreases with E0 while that of the perpendicular O2 increases, accounting for the nearly energy-independent O2 sticking probability determined previously by a randomly oriented O2 beam.
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高温选态分子氧束的研制及其在Pt(111)上o2吸附研究中的应用
单自旋-旋转状态选择[(J,M)=(2,2)]的O2束使我们能够进行自旋和取向控制的O2化学吸附实验。我们最近将其可用的平移能量范围扩大到0.10.9 eV。在本研究中,该光束被用于分析Pt(111)上的O2化学吸附。尽管由于其技术重要性,该系统已被深入研究,但低氧粘附概率的起源及其不寻常的能量依赖性仍不清楚。目前的结果表明,在低平动能(E0)条件下,直接活化的化学吸附只发生在O2轴几乎与表面平行的情况下。在高能量条件下(E0>0.5 eV),平行O2的粘附概率随E0的增大而减小,而垂直O2的粘附概率随E0的增大而增大,这就解释了之前随机定向O2束确定的几乎与能量无关的O2粘附概率。
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