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Formation of surface adspecies at furan and tetrahydrofuran adsorption on the Pt surface studied by work function changes and Auger electron spectroscopy

机译:通过功函数变化和俄歇电子能谱研究了呋喃和四氢呋喃在铂表面上吸附时表面形貌的形成

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The adsorption of tetrahydrofuran (THF) and furan (F) on polycrystalline Pt-foil has been studied by work function change (Δφ) measurements and Auger electron spectroscopy (AES). The results were compared with those obtained earlier for the adsorption of cyclic hydrocarbons. The general character of the adsorption process (i.e. the dependence of |Δφ| and C/Pt ratio on temperature and exposure, and the |Δφ| vs. C/Pt correlation) is similar to the one observed during adsorption of cyclic hydrocarbons. THF produces σ-bonded adspecies in a similar manner to cyclopentane. F forms first a π-bonded surface complex, as do benzene and toluene. The π-adsorbed species are then transformed into σ-bonded ones under exposure to excess F. The numeric values characterizing the adsorption of the two heterocycles (mainly the C/Pt values) differ substantially from those measured for the adsorption of cyclic hydrocarbons.
机译:通过功函数变化(Δφ)测量和俄歇电子能谱(AES)研究了四氢呋喃(THF)和呋喃(F)在多晶Pt箔上的吸附。将结果与先前获得的环烃吸附结果进行了比较。吸附过程的一般特征(即|Δφ|和C / Pt比值对温度和暴露的依赖性,以及|Δφ|与C / Pt的相关性)与在环烃吸附过程中观察到的相似。 THF以类似于环戊烷的方式产生σ键结合的甲酚。 F首先与苯和甲苯形成π键结合的表面配合物。然后,在过量的F下,π吸附的物质转变为σ键的物质。表征两个杂环的吸附的数值(主要是C / Pt值)与环烃的吸附所测得的数值明显不同。

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