纳米材料基催化剂
双金属片
材料科学
电催化剂
扫描透射电子显微镜
合金
八面体
纳米颗粒
化学工程
透射电子显微镜
原子单位
催化作用
结晶学
纳米技术
金属
电化学
化学
晶体结构
冶金
物理化学
电极
生物化学
物理
工程类
量子力学
作者
Chunhua Cui,Lin Gan,Marc Heggen,Stefan Rudi,Peter Strasser
出处
期刊:Nature Materials
[Springer Nature]
日期:2013-06-14
卷期号:12 (8): 765-771
被引量:1222
摘要
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.
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