Size and Composition Dependence of Oxygen Reduction Reaction Catalytic Activities of Mo-Doped PtNi/C Octahedral Nanocrystals

纳米晶 催化作用 八面体 纳米材料基催化剂 材料科学 化学 无机化学 氧化还原 化学工程 分析化学(期刊) 结晶学 纳米技术 物理化学 晶体结构 电化学 电极 工程类 生物化学 色谱法
作者
Shlomi Polani,Katherine E. MacArthur,Malte Klingenhof,Xingli Wang,Paul Paciok,Lujin Pan,Quanchen Feng,Attila Kormányos,Serhiy Cherevko,Marc Heggen,Peter Strasser
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:11 (18): 11407-11415 被引量:35
标识
DOI:10.1021/acscatal.1c01761
摘要

A variety of synthesis protocols for octahedral PtNi nanocatalysts have led to remarkable improvements in platinum mass and specific activities for the oxygen reduction reaction. Nevertheless, the values achieved are still only one tenth of the activity measured from Pt3Ni single-crystal (111) surfaces. These particles lose activity during potential cycling, primarily because of Ni leaching and subsequent loss of shape. Here, we present the syntheses and high catalytic oxygen reduction reaction activities of molybdenum-doped PtNi octahedral catalysts with different sizes (6–14 nm) and compositions. We show that the Mo-doped, Ni-rich, PtNi octahedral catalysts exhibit enhanced stability over their undoped counterpart. Scanning transmission electron microscopy with energy-dispersive X-ray analysis reveals the particular elemental distribution for the size and composition of the different catalysts. By combining high-resolution compositional analysis with electrochemical measurements and online inductively coupled plasma mass spectrometry, it was possible to correlate the size, morphology, and composition with the oxygen reduction reaction activities before and after accelerated stress tests. The octahedral catalysts show high electrochemical surface areas and increasing specific activity with increasing surface area of the (111) facets and Ni content, leading to high mass activities. These results demonstrate the advantages of increasing the (111) surface area and Ni content of PtNi nano-octahedral catalysts to improve the performance and stability for the oxygen reduction reaction.
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