Porous Hollow PtNi/C Electrocatalysts: Carbon Support Considerations To Meet Performance and Stability Requirements

材料科学 质子交换膜燃料电池 石墨烯 化学工程 催化作用 电化学 碳化物衍生碳 纳米颗粒 表面改性 纳米材料 比表面积 碳纤维 阴极 碳纳米管 介孔材料 碳纳米纤维 纳米技术 化学 电极 复合材料 复合数 有机化学 物理化学 工程类
作者
Tristan Asset,Nathalie Job,Yan Busby,Alexandre Crisci,Vincent Martin,Vaios Stergiopoulos,Céline Bonnaud,Alexey Serov,Plamen Atanassov,Raphaël Chattot,Laëtitia Dubau,Frédéric Maillard
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:8 (2): 893-903 被引量:64
标识
DOI:10.1021/acscatal.7b03539
摘要

The influence of the texture, structure, and chemistry of different carbon supports on the morphological properties, oxygen reduction reaction (ORR) activity, and stability of porous hollow PtNi nanoparticles (NPs) was investigated. The carbon nanomaterials included carbon blacks, carbon nanotubes, graphene nanosheets, and carbon xerogel and featured different specific surface areas, degrees of graphitization, and extent of surface functionalization. The external and inner diameters of the supported porous hollow PtNi/C NPs were found to decrease with an increase in the carbon mesopore surface area. Despite these differences, similar morphological properties and electrocatalytic activities for the ORR were reported. The stability of the synthesized electrocatalysts was assessed by simulating electrochemical potential variations occurring at a proton exchange membrane fuel cell (PEMFC) cathode during startup/shutdown events. Identical location transmission electron microscopy (IL-TEM) and electrochemical methods revealed the occurrence of a carbon-specific degradation mechanism: carbon corrosion into CO2 and particle detachment were noticed on carbon xerogels and graphene nanosheets while, on carbon blacks, surface oxidation prevailed (C → COsurf) and did not result in modified electrical resistance of the catalytic layers, rendering these carbon supports better suited to prepare highly active and stable ORR electrocatalysts.
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