首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >Electrochemical study of Pt-Pd, Pt-Ru, Pt-Rh and Pt-Sn/C in acid media for hydrogen adsorption-desorption reaction
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Electrochemical study of Pt-Pd, Pt-Ru, Pt-Rh and Pt-Sn/C in acid media for hydrogen adsorption-desorption reaction

机译:酸性介质中Pt-Pd,Pt-Ru,Pt-Rh和Pt-Sn / C的氢吸附-解吸反应的电化学研究

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摘要

Four platinum-based binary catalysts (Pt-Ru, Pt-Rh, Pt-Sn, Pt-Pd/C) used for hydrogen adsorption-desorption reaction were investigated by cyclic voltammetry in 0.5 M H_2SO_4 at room temperature. For all the metallic alloys the difference between the total anodic and cathodic charges (1 and 50 cycles) is related to the amount of second metal dissolution. Changes in surface composition during continuous potential cycling are also due to the preferential dissolution of a second metal component. Comparison of the changes in electrosorption properties with the amount of metal dissolved leads to the conclusion that the surface involved in chemisorption reactions consisted of no more than a few atomic layers. The good electrocatalytic behavior for the Pt-Ru/C system is only attributed to the synergic effect of the second metal, which can cause a strong hydrogen adsorption (Q_H~c). The particle sizes were also determinate by conventional physical dispersion method. This method enabled us to observe the shape and size of the particles by transmission electron microscopy (TEM).
机译:在室温下于0.5 M H_2SO_4循环伏安法研究了四种用于氢吸附-脱附反应的铂基二元催化剂(Pt-Ru,Pt-Rh,Pt-Sn,Pt-Pd / C)。对于所有金属合金,总的阳极电荷和阴极电荷之间的差异(1和50个循环)与第二种金属的溶解量有关。连续电势循环过程中表面成分的变化也归因于第二金属组分的优先溶解。通过比较电吸附性能与金属溶解量的变化,得出结论,参与化学吸附反应的表面不超过几个原子层。 Pt-Ru / C体系的良好电催化行为仅归因于第二种金属的协同作用,这可以引起强烈的氢吸附(Q_H〜c)。粒度也通过常规的物理分散方法确定。这种方法使我们能够通过透射电子显微镜(TEM)观察颗粒的形状和大小。

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