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The electrochemical oxidation of carbon monoxide adsorbed on Pt(111) in aqueous electrolytes as monitored by in situ potential step-second harmonic generation

机译:通过原位电位阶跃-次谐波生成监测的水电解质中Pt(111)上吸附的一氧化碳的电化学氧化

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The dynamics of electrooxidation of adsorbed CO on Pt(111) microfacets was examined in CO-saturated 0.1 M HClO_4 aqueous solutions by in situ time resolved second harmonic generation (SHG). Analysis of the temporal dependence of the intensity of the SHG signals recorded for experiments in which the potential was stepped to values high enough for adsorbed CO oxidation to ensue, was found to be consistent with the mean field theory model, yielding rate constants somewhat higher than those reported by Lebedeva et al. (N. P. Lebedeva, M.T.M.Koper, J.M.Feliu and R.A.v. Santen, J.Electroanal. Chem., 2002, 524-525, 242-251) in sulfuric acid solutions. The smaller rates observed by these authors may be ascribed to the presence of anions, i.e. in all likelihood bisulfate, which are capable of competing effectively for Pt sites thereby blocking formation of oxygenated specieson the surfce. Also discussed in this work are the virtues and limitations of in situ SHG for monitoring fast surface processes.
机译:通过原位时间分辨二次谐波生成(SHG),在CO饱和的0.1 M HClO_4水溶液中检查了吸附在Pt(111)微面上的CO的电氧化动力学。发现对实验记录的SHG信号强度的时间依赖性进行了分析,在该实验中,电势被逐步提高到足以引起吸附的CO氧化发生的值,这与平均场理论模型相符,产率常数高于Lebedeva等报道的那些。 (N.P. Lebedeva,M.T.M。Koper,J.M.Feliu和R.A.v. Santen,J.Electroanal.Chem。,2002,524-525,242-251)。这些作者观察到的较小比率可能归因于阴离子的存在,即很可能存在硫酸氢盐,它们能够有效竞争Pt位点,从而阻止表面上的氧化物种的形成。在这项工作中还讨论了原位SHG用于监测快速表面过程的优点和局限性。

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