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Potential dependence of segregation and surface alloy formation of a Ru modified carbon supported Pt catalyst

机译:Ru修饰碳负载Pt催化剂的偏析和表面合金形成的电位依赖性

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摘要

Ruthenium modified carbon supported platinum catalysts have been shown to have a similar activity towards carbon monoxide oxidation as conventionally prepared bimetallic PtRu alloy catalysts. In this study the effect of the applied electrode potential and potential cycles on the location and oxidation state of the Ru species in such Ru modified Pt/C catalysts was investigated using in situ EXAFS collected at both the Ru K and Pt L{sub}3 absorption edges. The as prepared catalyst was found to consist of a Pt core with a Ru oxy/hydroxide shell. The potential dependent data indicated alloying to form a PtRu phase at 0.05 V versus RHE and subsequent dealloying to return to the Ru oxy/hydroxide decorated Pt surface at potentials greater than 0.7 V. The Ru-O distances obtained indicate that both Ru{sup}(3+) and Ru{sup}(4+) species are present on the surface of the Pt particles at oxidising potentials; the former is characteristic of the as prepared Ru modified Pt/C catalyst and following extensive periods at potentials above 0.7 V and the latter of the Ru oxide species on the PtRu alloy.
机译:钌改性的碳载铂催化剂已显示出与常规制备的双金属PtRu合金催化剂相似的一氧化碳氧化活性。在这项研究中,使用在Ru K和Pt L {sub} 3处收集的原位EXAFS,研究了施加的电极电势和电势循环对Ru修饰的Pt / C催化剂中Ru物种的位置和氧化态的影响。吸收边缘。发现所制备的催化剂由具有Ru氧基/氢氧化物壳的Pt核组成。与电位相关的数据表明,与RHE相比,在0.05 V时合金化形成PtRu相,随后在高于0.7 V的电位下脱合金返回到Ru氧/氢氧化物修饰的Pt表面。获得的Ru-O距离表明,两个Ru {sup} (3+)和Ru {sup}(4+)物种以氧化电位存在于Pt颗粒的表面上。前者是所制备的Ru改性Pt / C催化剂的特征,并且在0.7 V以上的电势下经过很长一段时间后,PtRu合金上的Ru氧化物种类也很晚。

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