An electron energy loss spectroscopic study of ethylene chemisorbed on Pd(110) at 110 K

Michael A. Chesters, Gordon S. McDougall , Martyn E. Pemble , Norman Sheppard
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引用次数: 2

Abstract

Adsorption of ethylene on the (110) surface of palladium at 110 K gives rise to two related but clearly distinguishable types of electron energy loss (EEL) spectra corresponding to low and high coverage. Most features in the spectra in both coverage regimes can be interpreted in terms of a π-complex of ethylene with the metal surface. Analysis of the corresponding ethylene-d4 EEL spectra and comparison with infrared, Raman and inelastic neutron scattering data for the analogous ethylene complex, Zeise's salt, supports this assignment. The selection rules applicable to dipole and impact scattering both on- and off-specular are employed to determine the orientation of the π-complexes with respect to the surface. At higher coverages additional loss features are observed. These are interpreted in terms of the presence of a small proportion of σ-diadsorbed ethylene complexes bonded to pairs of metal atoms.

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乙烯在110 K下在Pd(110)上化学吸附的电子能量损失谱研究
乙烯在钯(110)表面在110 K下的吸附产生了两种相关但明显可区分的电子能量损失(EEL)谱,对应于低覆盖率和高覆盖率。在两种覆盖体系下,光谱中的大部分特征都可以用乙烯与金属表面的π配合物来解释。分析相应的乙烯-d4 EEL光谱,并与类似的乙烯配合物(Zeise’s salt)的红外、拉曼和非弹性中子散射数据进行比较,支持这一指派。适用于偶极子散射和冲击散射的选择规则被用于确定π配合物相对于表面的取向。在较高的覆盖率下,可以观察到额外的损失特征。这些解释是由于存在一小部分的σ-二吸附乙烯配合物与金属原子对结合。
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