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Enhancing the Electrocatalytic Activity of Pd/M (M = Ni, Mn) Nanoparticles for the Oxygen Reduction Reaction in Alkaline Media through Electrochemical Dealloying

机译:通过电化学欠入扩张通过电化学造影增强碱性培养基中的氧还原反应的Pd / m(m = ni,mn)纳米粒子的电催化活性

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We have developed a facile and effective electrochemical dealloying strategy to enhance the electrocatalytic activity of Pd/M (M = Ni, Mn) nanoparticles for the oxygen reduction reaction (ORR) in alkaline media. The enhancement arises from the higher atomic concentration of electrochemically active Pd exposed on the surface of the nanoparticles as a result of the electrochemical dealloying process, which was verified by electron energy loss spectroscopy elemental mapping, X-ray photoelectron spectroscopy, and CO stripping. These dealloyed catalysts also showed a negligible decrease in the ORR activity after 4000 potential cycles in alkaline media. In addition, after the degradation that resulted from extended potential cycles in alkaline media, the ORR activity of the catalysts could be restored by repeating the dealloying procedures, with only a 14 mV decrease in the half-wave potential after 16,000 cycles for dealloyed PdNi/C. Similar results were obtained for PdMn/C. These findings provide insights for the rational design of the composition and structure of electrocatalysts with higher atomic utilization of active materials and enhanced electrocatalytic activity, based on postsynthesis modification methods.
机译:我们开发了一种容易和有效的电化学蓄能策略,以增强碱性介质中的氧还原反应(ORR)的Pd / m(m = Ni,Mn)纳米颗粒的电催化活性。由于电化学欠入扩张工艺,从纳米颗粒表面上暴露在纳米颗粒表面上的电化学活性PD的较高原子浓度产生的增强,其通过电子能损光谱元素映射,X射线光电子体光谱和CO剥离验证。这些易用的催化剂还显示出在碱性介质中4000个潜在循环后的ORR活性可忽略不计。另外,在碱性介质中延长电位循环导致的降解之后,可以通过重复脱债手术来恢复催化剂的ORR活性,在17,000个循环的半波潜力下,仅为14mV的解放PDNI / C。获得类似的结果,用于PDMN / C.这些调查结果为基于后二合成改性方法提供了具有更高的原子用途和增强的电催化活性的电催化剂的合成和结构的合理设计的见解。

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