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首页> 外文期刊>Electrochimica Acta >Origin of efficient oxygen reduction reaction on Pd monolayer supported on Pd-M (M=Ni, Fe) intermetallic alloy
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Origin of efficient oxygen reduction reaction on Pd monolayer supported on Pd-M (M=Ni, Fe) intermetallic alloy

机译:PD-M(M = Ni,Fe)金属间合金的Pd单层上有效氧还原反应的起源

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Intermetallic alloy has become a hot topic in heterogeneous catalysis due to improved activity and stability. We report here the results of Pd monolayer supported on face-centered tetragonal (fct) Pd-M (M?=?Ni or Fe) intermetallic alloy as cathode materials by first principle calculations. Adsorbed O2is found to undergo hydrogenation process into OOH instead of direct dissociative mechanism. The oxygen reduction reaction (ORR) proceeds via four-electron transfer pathway on both surfaces. The enhanced activities are ascribed to moderate adsorption strength for ORR intermediates due to compression strain and substrate electron transfer. The dissolution potential analysis indicates that both Pd/PdNi(111) and Pd/PdFe(111) are stable under operating condition. Gibbs free energy analysis and barrier calculations suggest that the proposed Pd monolayer structures are promising for cathode material. These results can be useful in designing intermetallic Pd-M alloy as ORR electrocatalysts.
机译:由于改善的活性和稳定性,金属间合金已成为异质催化的热门话题。 我们在此报告PD单层的结果,通过第一原理计算,PD单层支撑在面向中心的四方(FCT)Pd-M(M?=Δni或Fe)金属间合金中作为阴极材料。 发现吸附的O2是将氢化过程进行成OOH而不是直接分离机制。 氧还原反应(ORR)通过两个表面上的四电子转移途径进行。 由于压缩应变和基材电子转移,增强的活性为适度的吸附强度进行适度的orr中间体。 溶出电位分析表明PD / PDNI(111)和PD / PDFE(111)都在操作条件下稳定。 GIBBS自由能量分析和屏障计算表明,所提出的PD单层结构是对阴极材料的承诺。 这些结果可用于将金属间PD-M合金设计为ORR电催化剂。

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