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Noble-Metal based Metallic Glasses as Highly Catalytic Materials for Hydrogen Oxidation Reaction in Fuel Cells

机译:贵金属基金属玻璃作为燃料电池中氢氧化反应的高催化材料

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摘要

Electro-catalyst design with superior performance and reduced precious metal content (compared to state-of-the-art Pt/C) has been a challenge in proton exchange membrane fuel cells, preventing their widespread adoption. Metallic glasses have recently shown promising performance and large electrochemical surface area in catalytic reactions. The electro-catalytic behavior of recently developed Pt-, Pd-, and Pt/Pd-based metallic glasses was evaluated in this study using scanning electrochemical microscopy. The influence of chemistry and electronic structure on catalytic behavior was studied using scanning kelvin probe technique. The work function for the metallic glasses was lower by 75 mV to 175 mV compared to pure Pt. This resulted in higher catalytic activity for the amorphous alloys, which was attributed to the ease of charge transfer on the surface. The binding energy for the metallic glasses, measured using X-ray photoelectron spectroscopy, was higher by 0.2 eV to 0.4 eV. This explained easier removal of adsorbed species from the surface of amorphous alloys. The synergistic effect of Pt and Pd in alloys containing both the noble metals was demonstrated towards hydrogen oxidation reaction.
机译:具有优异性能和降低的贵金属含量(与最新的Pt / C相比)的电催化剂设计一直是质子交换膜燃料电池面临的挑战,阻碍了其广泛采用。金属玻璃最近在催化反应中显示出有希望的性能和大的电化学表面积。在这项研究中使用扫描电化学显微镜评估了最近开发的基于Pt,Pd和Pt / Pd的金属玻璃的电催化行为。使用扫描开尔文探针技术研究了化学和电子结构对催化行为的影响。与纯Pt相比,金属玻璃的功函降低了75 mV至175 mV。这导致非晶态合金具有更高的催化活性,这归因于表面电荷转移的容易性。使用X射线光电子能谱法测得的金属玻璃的结合能高0.2 eV至0.4 eV。这解释了更容易从非晶态合金表面去除吸附的物质。在同时含有两种贵金属的合金中,Pt和Pd的协同作用被证明对氢氧化反应具有协同作用。

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