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Carbon monoxide oxidation and nitrous oxide reduction on Rh/Pt(111) electrodes

机译:Rh / Pt(111)电极上的一氧化碳氧化和一氧化二氮还原

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Rhodium adlayers on Pt(111) substrates have been prepared by electrodeposition from dilute Rh{sup}(3+) acidic solutions. Resulting deposition rates are lower than 0.03 ML min{sup}(-1). Pseudomorphic growth of the first monolayer has been confirmed by scanning tunneling microscopy (STM) as well as the formation of small compact islands in the submonolayer range. Carbon monoxide oxidation and nitrous oxide reduction have been studied on Rh/Pt(111) electrodes. The oxidation of carbon monoxide is catalyzed by the presence of very low coverages of rhodium as demonstrated by the negative shift of the CO oxidation profile. Results are compatible with a bifunctional mechanism for catalysis including CO diffusion in the Pt domains toward the edges of the islands (splitting of the voltammetric oxidation profile). The reduction of nitrous oxide occurs at different potential and with different rates on Pt domains, at the center of the Rh islands and at their edges, being the latter sites especially active. In any case, the adsorptive and catalytic activity of the adlayers differ from those of the bulk Pt(111) and Rh(111) electrodes. The existence of strain in the film together with a diminution in the coordination number for adatoms at the edges of the islands are considered to be at the origin of the observed behavior.
机译:通过从稀Rh {sup}(3+)酸性溶液中进行电沉积,可以在Pt(111)基板上制备铑添加剂。产生的沉积速率低于0.03 ML min {sup}(-1)。通过扫描隧道显微镜(STM)以及亚单分子层范围内的小致密岛的形成,证实了第一单分子层的假晶生长。在Rh / Pt(111)电极上研究了一氧化碳的氧化和一氧化二氮的还原。一氧化碳的氧化是由于铑的覆盖率很低而引起的,如CO氧化曲线的负移所证明的。结果与双功能催化机制兼容,该机制包括CO在Pt域中向岛边缘扩散(伏安氧化曲线分裂)。一氧化二氮的还原以不同的电位和不同的速率发生在Rh岛的中心及其边缘的Pt域上,后者的位置特别活跃。在任何情况下,吸附层的吸附和催化活性都不同于块状Pt(111)和Rh(111)电极的吸附和催化活性。膜中应变的存在以及在岛的边缘处的吸附原子的配位数的减少被认为是观察到的行为的起源。

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