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Methanol electrochemical oxidation at nanometer-scale PtRu materials

机译:纳米级PtRu材料的甲醇电化学氧化

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The electrochemical oxidation of CH3OH at nanometer-scale PtRu catalyst materials is reported. Comparisons are made between the properties of a Johnson Matthey (JM) PtRu black sample (50 at.% Ru (X-Ru approximate to 0.5)) and PtRu particles (2-6 nm, nominally X-Ru approximate to 0.5) prepared by sonication under anhydrous conditions. Cyclic voltammetry and in situ infrared spectroscopy measurements show the catalysts are active for the oxidation of 0.5 M CH3OH in 0.1 M HClO4 at temperatures between ambient and 70 degreesC. The sonochemically prepared PtRu sample displayed properties characteristic of bulk PtRu alloys with X-Ru approximate to 0.5. Evidence for phase separation of Pt and Ru was observed in CO stripping voltammetry from the JM catalyst adsorbed at low metal loadings (20 mug/cm(2)) on bulk Au electrodes. Per gram of catalyst, the JM material was more active toward CO, formation and displayed greater resistance to poisoning by adsorbed CO than the sonochemically prepared material during ambient temperature oxidation of 0.5 M CH3OH in 0.1 M HClO4. (C) 2004 Elsevier B.V. All rights reserved.
机译:报道了在纳米级PtRu催化剂材料上CH 3 OH的电化学氧化。在Johnson Matthey(JM)PtRu黑色样品(50 at。%Ru(X-Ru大约为0.5))和PtRu颗粒(2-6 nm,名义上X-Ru大约为0.5)的性能之间进行了比较。在无水条件下进行超声处理。循环伏安法和原位红外光谱法测量表明,该催化剂在环境温度至70℃之间的温度下,可在0.1 M HClO4中氧化0.5 M CH3OH。超声化学制备的PtRu样品显示了X-Ru约为0.5的块状PtRu合金的性能特征。在CO溶出伏安法中,从以低金属含量(20 mug / cm(2))吸附在块状Au电极上的JM催化剂中观察到Pt和Ru相分离的证据。对于每克催化剂,在环境温度下0.1 M HClO4中0.5 M CH3OH氧化过程中,JM材料对CO的形成更具活性,并且比声化学制备的材料表现出更大的抗吸附CO中毒的能力。 (C)2004 Elsevier B.V.保留所有权利。

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