Spanos Ioannis, Dideriksen Knud, Kirkensgaard Jacob J K, Jelavic Stanislav, Arenz Matthias
Nano-science Center, Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100 Copenhagen Ø, Denmark.
Niels Bohr Institute, University of Copenhagen, Universitetsparken 5, DK-2100, Copenhagen Ø, Denmark.
Phys Chem Chem Phys. 2015 Nov 14;17(42):28044-53. doi: 10.1039/c4cp04264f.
Platinum bimetallic alloys are well-known for their ability to catalyze the oxygen reduction reaction (ORR) in proton exchange membrane fuel cells (PEMFCs). Pt(x)Co(1-x) colloidal nanoparticles were synthesized with varying initial Pt : Co ratios, but constant size to investigate how the initial metal composition affects their electrocatalytic performance. The results show that upon contact with acid environment the Co leaches out of the particles leading to almost identical compositions, independent of the initial differences. Surprisingly the data show a clear trend in ORR activity, although the Pt(x)Co(1-x) nanoparticles almost completely de-alloy during acid leaching, i.e. under reaction conditions in a fuel cell. To scrutinize the resulting particle structure after de-alloying we used pair distribution function (PDF) analysis and X-ray diffraction (XRD) gaining insight into the structural disorder and its dependence on the initial metal composition. Our results suggest that not only the ORR activity, but also the corrosion resistance of the synthesized NPs, are dependent on the structural disorder resulting from the de-alloying process.
铂双金属合金以其在质子交换膜燃料电池(PEMFC)中催化氧还原反应(ORR)的能力而闻名。合成了具有不同初始Pt : Co比例但尺寸恒定的Pt(x)Co(1-x)胶体纳米颗粒,以研究初始金属组成如何影响其电催化性能。结果表明,在与酸性环境接触时,Co从颗粒中浸出,导致组成几乎相同,与初始差异无关。令人惊讶的是,数据显示出ORR活性的明显趋势,尽管Pt(x)Co(1-x)纳米颗粒在酸浸过程中几乎完全脱合金,即在燃料电池的反应条件下。为了仔细研究脱合金后所得颗粒的结构,我们使用了对分布函数(PDF)分析和X射线衍射(XRD),深入了解结构无序及其对初始金属组成的依赖性。我们的结果表明,不仅ORR活性,而且合成纳米颗粒的耐腐蚀性,都取决于脱合金过程产生的结构无序。