铂镍纳米粒子结构对燃料电池电催化氧化反应的影响

Nicolas Ishiki Ishiki/Nicolas, Maria Della-Costa Della-Costa/Maria, Beatriz Keller Keller/Beatriz, Kepler Rocha Rocha/Kepler, Francielle Bortoloti Bortoloti/Francielle, Antonio Angelo Angelo/Antonio
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摘要

本文研究了双金属纳米粒子(NPs)的聚集如何影响表面吸附位点的电子状态,进而影响材料在碱性介质中进行燃料电氧化时的性能。首先,我们合成了三种构型的铂镍 NPs:有序金属间化合物、普通合金和核壳。这些 NPs 中的铂和镍原子比接近 1:1。它们的颗粒大小相似,因此我们可以在不受这些物理参数影响的情况下评估它们的性能。根据 NP 中铂原子和镍原子的结构排列,表面吸附位点(铂)的电子条件发生了显著变化。因此,在碱性溶液中用作氢、甲醇、乙醇、乙二醇和甘油电氧化的阳极材料时,这些材料的性能也各不相同。表面位点的电子条件对反应物、中间产物和产物的吸附特性有很大影响,从而影响材料在电化学过程中的性能。本文采用的方法有助于更好地理解电催化过程和设计选择性电催化剂。
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Impact of Pt-Ni Nanoparticle Architecture on Electrocatalytic Oxidation Reaction in Fuel Cells
This paper investigates how the aggregation of bimetallic nanoparticles (NPs) influences the electronic condition of the surface adsorption site and, hence, the performance of materials during the electrooxidation of fuels in an alkaline medium. First, we synthesized Pt-Ni NPs in three configurations: ordered intermetallic, ordinary alloy, and core-shell. The NPs contained Pt and Ni close to a 1:1 Pt/Ni atomic ratio. They had similar particle sizes, which allowed us to evaluate their performance without the influence of these physical parameters. Depending on the structural arrangement of the Pt and Ni atoms in the NP, the electronic condition of the surface adsorption site (Pt) changed significantly. Consequently, the performance of the materials varied whenever they were used as anode material for the electrooxidation of hydrogen, methanol, ethanol, ethylene glycol, and glycerol in an alkaline solution. The electronic condition of the surface site strongly affected the adsorption characteristics of the reactants, intermediates, and products, consequently impacting the material's performance during the electrochemical processes. The approach adopted here could contribute to a better understanding of electrocatalytic processes and the design of selective electrocatalysts.
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