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Characterization of vacant coordination sites of cations on the surfaces of oxides and zeolites using infrared spectroscopy of adsorbed probe molecules

机译:使用吸附的探针分子的红外光谱表征氧化物和沸石表面上阳离子的空位配位点

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摘要

A critical review is given of the application of IR spectroscopy of small adsorbed probe molecules such as CO and N_2 for the determination of the coordination state of surface cations on oxides and zeolites. Special emphasis is devoted to the different kinds of geminal species. So-called complex-specified geminal species are formed as a result of stabilization of the structure by different factors (stable electron configuration, strong ligand-ligand interaction, etc.). During the decomposition of these species linear intermediates are not produced. When complex-specified geminal species are formed, direct conclusions on the original coordination state of the coordinatively unsaturated adsorption site can not be drawn. Site-specified geminal species are produced as a result of low coordination of the adsorption site. These species loose their ligands stepwise and show a tendency to form mixed-ligand species. Site-specified geminal complexes are typically formed with cation-exchanged zeolites, particularly with bulky cations having large radii. Analysis of adsorption isotherms of surface complexes bearing either one or more adsorbate molecules is performed and practical hints for their use are proposed. Finally, possible future directions of the research on this topic are summarized.
机译:对红外光谱法在吸附的小分子探针(如CO和N_2)用于测定氧化物和沸石上的表面阳离子配位态的应用方面进行了严格的审查。特别强调的是不同种类的双子物种。由于不同因素(稳定的电子构型,强大的配体-配体相互作用等)而使结构稳定,因此形成了所谓的复杂复合双物种。在这些物质的分解过程中,不会产生线性中间体。当形成复杂的双物种时,无法得出关于不饱和配位吸附位点原始配位状态的直接结论。由于吸附位点的低配位而产生了特定位点的宝石物种。这些物质逐步失去其配体,并显示出形成混合配体物质的趋势。特定位置的宝石配合物通常与阳离子交换沸石,特别是与具有大半径的大体积阳离子形成。进行了带有一个或多个被吸附物分子的表面配合物的吸附等温线分析,并提出了使用它们的实用提示。最后,总结了该主题研究的未来可能方向。

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