Department of Physics and Astronomy, Aarhus University, Interdisciplinary Nanoscience Center, DK-8000 Aarhus C, Denmark.
ACS Nano. 2010 Aug 24;4(8):4380-7. doi: 10.1021/nn101241c.
From an interplay between scanning tunneling microscopy, temperature programmed desorption, X-ray photoelectron spectroscopy, and density functional theory calculations we have studied low-temperature CO oxidation on Au/Ni(111) surface alloys and on Ni(111). We show that an oxide is formed on both the Ni(111) and the Au/Ni(111) surfaces when oxygen is dosed at 100 K, and that CO can be oxidized at 100 K on both of these surfaces in the presence of weakly bound oxygen. We suggest that low-temperature CO oxidation can be rationalized by CO oxidation on O(2)-saturated NiO(111) surfaces, and show that the main effect of Au in the Au/Ni(111) surface alloy is to block the formation of carbonate and thereby increase the low-temperature CO(2) production.
通过扫描隧道显微镜、程序升温脱附、X 射线光电子能谱和密度泛函理论计算的相互作用,我们研究了低温 CO 在 Au/Ni(111)表面合金和 Ni(111)上的氧化。我们表明,当在 100 K 下注入氧气时,Ni(111)和 Au/Ni(111)表面都会形成氧化物,并且在存在弱结合氧的情况下,CO 可以在这两种表面上于 100 K 下被氧化。我们认为,低温 CO 氧化可以通过 CO 在 O(2)-饱和 NiO(111)表面上的氧化来合理化,并表明 Au 在 Au/Ni(111)表面合金中的主要作用是阻止碳酸盐的形成,从而增加低温 CO(2)的生成。