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首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >The driving force for (p * √3) <-> (1 * 1) phase transition of Au(111) in the presence of organic adsorption: a combined chronocoulometric and surface X-ray scattering study
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The driving force for (p * √3) <-> (1 * 1) phase transition of Au(111) in the presence of organic adsorption: a combined chronocoulometric and surface X-ray scattering study

机译:在存在有机吸附的情况下Au(111)的(p *√3)<->(1 * 1)相变的驱动力:计时容积法和表面X射线散射研究

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摘要

In situ X-ray scattering and chronocoulometric experiments were performed to assess the influence of adsorption of pyridine, 2,2'-bipyridine and uracil on the driving force for the (p * √3) → (1 * 1) transition of the Au(111) surface. We have shown that the overall driving force is a combination of the two driving forces and have given the upper and lower limits to this estimate. Our results show that the two driving forces are of comparable magnitude and that the interpretation of the surface reconstruction phenomena given in terms of either purely charge or a purely adsorbate effect is an oversimplification.
机译:进行了原位X射线散射和计时库仑实验,以评估吡啶,2,2'-联吡啶和尿嘧啶的吸附对Au(p *√3)→(1 * 1)跃迁的驱动力的影响。 (111)表面。我们已经表明,总驱动力是两个驱动力的组合,并且已对此估计值给出了上限和下限。我们的结果表明,这两个驱动力的大小相当,并且对根据纯电荷或纯吸附作用给出的表面重建现象的解释过于简单。

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