The Electrochemical Energy, Catalysis, and Materials Science Laboratory, Department of Chemistry, Chemical Engineering Division, Technical University Berlin, Berlin 10623, Germany.
Nat Mater. 2013 Aug;12(8):765-71. doi: 10.1038/nmat3668. Epub 2013 Jun 16.
Shape-selective monometallic nanocatalysts offer activity benefits based on structural sensitivity and high surface area. In bimetallic nanoalloys with well-defined shape, site-dependent metal surface segregation additionally affects the catalytic activity and stability. However, segregation on shaped alloy nanocatalysts and their atomic-scale evolution is largely unexplored. Exemplified by three octahedral PtxNi1-x alloy nanoparticle electrocatalysts with unique activity for the oxygen reduction reaction at fuel cell cathodes, we reveal an unexpected compositional segregation structure across the {111} facets using aberration-corrected scanning transmission electron microscopy and electron energy-loss spectroscopy. In contrast to theoretical predictions, the pristine PtxNi1-x nano-octahedra feature a Pt-rich frame along their edges and corners, whereas their Ni atoms are preferentially segregated in their {111} facet region. We follow their morphological and compositional evolution in electrochemical environments and correlate this with their exceptional catalytic activity. The octahedra preferentially leach in their facet centres and evolve into 'concave octahedra'. More generally, the segregation and leaching mechanisms revealed here highlight the complexity with which shape-selective nanoalloys form and evolve under reactive conditions.
具有特定形状的单金属纳米催化剂具有基于结构敏感性和高表面积的活性优势。在具有明确形状的双金属纳米合金中,依赖于位置的金属表面偏析还会影响催化活性和稳定性。然而,对于形状合金纳米催化剂及其原子尺度演化的偏析,目前还在很大程度上尚未被探索。我们通过三个具有独特氧还原反应活性的八面体 Pt x Ni 1-x 合金纳米粒子电催化剂为例,使用具有相位差校正功能的扫描透射电子显微镜和电子能量损失光谱揭示了在{111}面上出人意料的组成偏析结构。与理论预测相反,原始的 Pt x Ni 1-x 纳米八面体在其边缘和拐角处具有富 Pt 框架,而 Ni 原子则优先在其{111}面区域偏析。我们跟踪了它们在电化学环境中的形态和组成演化,并将其与它们异常的催化活性相关联。八面体优先在其面心溶出,并演变成“凹八面体”。更一般地,这里揭示的偏析和溶出机制强调了在反应条件下形状选择性纳米合金形成和演化的复杂性。