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Electroactivity of Pt-Ru/polyaniline composite catalyst-electrodes prepared by electrochemical deposition methods

机译:电化学沉积法制备的Pt-Ru /聚苯胺复合催化剂-电极的电活性

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The electrochemical deposition of Pt-Ru nanoparticles on conducting polymer supports and carbon supports, as well as their electro-catalytic activities, were investigated. Pt-Ru catalysts of 3-8 nm average size were grown on supports by step-potential plating methods. The catalysts' loading contents were enhanced by increasing the plating time of the deposition method. Polyaniline and carbon blacks (CBs) were selected and compared as catalyst supports. The particle sizes and morphological structures of the Pt-Ru/support catalysts were evaluated using X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical behaviors of the Pt-Ru/support catalysts for methanol oxidation were investigated according to their characteristic current-voltage curves and chronoamperometry in a methanol solution. As a result, the electrochemical activity was enhanced with increased plating time, reaching the maximum at 24 min, and then decreased. The specific current density for the polyaniline-supported catalysts was higher than that for the CBs-supported ones. The enhanced catalytic activity was related to the higher electrical conductivity of the polyaniline, the increased electrochemical surface area of catalysts, or the higher ion diffusion behaviours. (c) 2008 Elsevier B.V. All rights reserved.
机译:研究了Pt-Ru纳米粒子在导电聚合物载体和碳载体上的电化学沉积及其电催化活性。通过分步电势电镀法在载体上生长平均尺寸为3-8 nm的Pt-Ru催化剂。通过增加沉积方法的电镀时间,可以提高催化剂的负载量。选择聚苯胺和炭黑(CBs)并将其作为催化剂载体进行比较。使用X射线衍射(XRD)和透射电子显微镜(TEM)评估了Pt-Ru /载体催化剂的粒度和形态结构。根据Pt-Ru /载体催化剂在甲醇溶液中的特征电流-电压曲线和计时电流法,研究了甲醇催化氧化Pt-Ru /载体催化剂的电化学行为。结果,电化学活性随电镀时间的增加而增强,在24分钟时达到最大值,然后下降。聚苯胺负载的催化剂的比电流密度高于CBs负载的催化剂。增强的催化活性与聚苯胺的较高电导率,催化剂的电化学表面积增加或较高的离子扩散行为有关。 (c)2008 Elsevier B.V.保留所有权利。

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