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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >An Investigation of Structure-Catalytic Activity Relationship for Pt-Co/C Bimetallic Nanoparticles toward the Oxygen Reduction Reaction
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An Investigation of Structure-Catalytic Activity Relationship for Pt-Co/C Bimetallic Nanoparticles toward the Oxygen Reduction Reaction

机译:Pt-Co / C双金属纳米粒子对氧还原反应的结构-催化活性关系的研究

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摘要

Carbon-supported Pt-Co alloy nanoparticle catalysts of nominal atomic composition but with different alloying extents were prepared via a modified Watanabe process by employing microwave heating. Their structure was studied by X-ray diffraction (XRD) and X-ray absorption spectroscopy (XAS) techniques. Transmission electron microscopy (TEM) images indicated that the in-house-prepared Pt-Co alloy nanoparticles (sample-1 and sample-2) were well dispersed on the surface of the carbon support with narrow particle size distribution which is consistent with XRD grain size values. The catalyst composition obtained from XAS was nearly the same as that of the nominal value (1:1). The alloying extent values of Pt calculated from XAS measurements for sample-2 is similar to that of the commercial E-tek Pt-Co/C. This observation demonstrates the practical viability of our preparation protocol for Pt-Co/C catalysts. A comparative study was made for the oxygen reduction reaction (ORR) using a thin-film rotating disk electrode method to evaluate the catalytic behavior of Pt-Co/C and Pt/C catalyst with similar metal loadings and particle sizes. As compared to the Pt/C catalyst, the bimetallic Pt-Co/C of sample-2 exhibited an enhancement factor of 3 in mass activity at 0.95 V toward ORR. The enhancement in activity of sample-2 is similar in magnitude to that of the commercial E-tek Pt- Co/C catalyst. It is found that that the samples possessing a high alloying extent of Pt in the cluster enhances the activity of the bimetallic Pt-Co/C toward ORR. This observation confirms that the alloying extent of Pt is an important parameter by which one can have control over the fine-tuning of the catalytic activities of bimetallic nanoclusters. This activity enhancement may originate from the favorable electronic effects of a well mixed alloy underneath a thin "Pt-rich skin" structure of the Pt-Co bimetallic nanoparticles. This kind of thin "Pt-rich skin" is created by the dissolution of Co oxide on Pt-Co bimetallic nanoparticles while washing in acidic electrolyte before being subjected to ORR.
机译:通过改进的渡边工艺,通过微波加热,制备了标称原子组成但具有不同合金化程度的碳载Pt-Co合金纳米颗粒催化剂。通过X射线衍射(XRD)和X射线吸收光谱(XAS)技术研究了它们的结构。透射电子显微镜(TEM)图像表明,内部制备的Pt-Co合金纳米颗粒(样品1和样品2)很好地分散在碳载体表面上,具有窄的粒度分布,这与XRD晶粒一致大小值。由XAS获得的催化剂组成与标称值(1:1)几乎相同。根据样品2的XAS测量计算得出的Pt合金化程度值与商业E-tek Pt-Co / C相似。该观察结果证明了我们制备Pt-Co / C催化剂的方案的实际可行性。使用薄膜转盘电极法对氧还原反应(ORR)进行了比较研究,以评估具有相似金属负载和粒径的Pt-Co / C和Pt / C催化剂的催化性能。与Pt / C催化剂相比,样品2的双金属Pt-Co / C在对ORR的0.95 V电压下的质量活度提高了3。样品2活性的增强在幅度上与商业E-tek Pt-Co / C催化剂的增强相似。发现在簇中具有高Pt合金化程度的样品增强了双金属Pt-Co / C对ORR的活性。这一观察结果证实,Pt的合金化程度是一个重要参数,通过它可以控制双金属纳米团簇的催化活性的微调。这种活性的提高可能源于在Pt-Co双金属纳米颗粒的薄的“富含Pt的表皮”结构下,充分混合的合金的有利电子效应。这种薄的“富Pt皮肤”是通过在经受ORR之前在酸性电解质中洗涤时,Co氧化物溶解在Pt-Co双金属纳米颗粒上而产生的。

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