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Characterization and evaluation of Pt-Ru catalyst supported on multi-walled carbon nanotubes by electrochemical impedance

机译:电化学阻抗法表征多壁碳纳米管负载的Pt-Ru催化剂

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In this work the authors present the results of a systematic characterization and evaluation of the carbon nanotube supported Pt-Ru (Pt-Ru/CNT) for its use as methanol oxidation catalyst. Its activity was compared with that of Pt and Pt-Ru catalysts supported on Vulcan and synthesized from carbonyl precursors, and another commercial Pt-Ru catalyst. The cyclic voltammetry, CO stripping and electrochemical impedance techniques were employed to determine the electrocatalytic activity of the catalysts. The electrochemical studies were performed in 0.5 M H_2SO_4 containing different concentrations of methanol (0.05-1 M). The results showed a noticeable influence of the catalyst support (CNT) on the performance of the catalyst for CO oxidation. The electrochemical impedance studies allowed us to separate the different steps in the methanol oxidation reaction and to control these steps or reactions by varying the applied potential and the methanol concentration. At low methanol concentration and potentials the de-hydrogenation of methanol predominated. But, at high potential and methanol concentrations, the CO oxidation predominated. These results allowed us to clearly describe at what potential and concentration ranges the bi-functional effect of Ru becomes evident. Our results indicated that the CO oxidation occurs both on Pt and Ru. Compared to other catalysts, Pt-Ru supported on carbon nanotubes showed superior catalytic activity for CO and methanol oxidation.
机译:在这项工作中,作者提出了系统表征和评估碳纳米管负载的Pt-Ru(Pt-Ru / CNT)用作甲醇氧化催化剂的结果。将其活性与负载在Vulcan上并由羰基前体合成的Pt和Pt-Ru催化剂以及另一种商用Pt-Ru催化剂的活性进行了比较。采用循环伏安法,CO汽提和电化学阻抗技术确定催化剂的电催化活性。电化学研究是在含有不同浓度甲醇(0.05-1 M)的0.5 M H_2SO_4中进行的。结果表明催化剂载体(CNT)对用于CO氧化的催化剂性能的显着影响。电化学阻抗研究使我们能够分离甲醇氧化反应中的不同步骤,并通过改变施加的电势和甲醇浓度来控制这些步骤或反应。在低甲醇浓度和电位下,甲醇的脱氢作用占主导。但是,在高电位和甲醇浓度下,CO氧化占主导地位。这些结果使我们能够清楚地描述在什么电位和浓度范围内Ru的双功能效应变得明显。我们的结果表明,CO氧化同时在Pt和Ru上发生。与其他催化剂相比,负载在碳纳米管上的Pt-Ru对CO和甲醇的氧化表现出优异的催化活性。

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