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首页> 外文期刊>ACS applied materials & interfaces >Visualization Analysis of Pt and Co Species in Degraded Pt3Co/C Electrocatalyst Layers of a Polymer Electrolyte Fuel Cell Using a Same-View Nano-XAFS/STEM-EDS Combination Technique
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Visualization Analysis of Pt and Co Species in Degraded Pt3Co/C Electrocatalyst Layers of a Polymer Electrolyte Fuel Cell Using a Same-View Nano-XAFS/STEM-EDS Combination Technique

机译:用相同视网膜XAFS /茎EDS组合技术在聚合物电解质燃料电池降解PT3Co / C电催化剂层中Pt和Co物种的可视化分析

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摘要

In order to obtain a suitable design policy for the development of a next-generation polymer electrolyte fuel cell, we performed a visualization analysis of Pt and Co species following aging and degradation processes in membrane-electrode assembly (MEA), using a same-view. Nano-X-ray absorption fine structure (XAFS)/Scanning transmission electron microscope (STEM)-energy dispersive X-ray spectroscopy (EDS) technique that we developed to elucidate durability factors and degradation mechanisms of a MEA Pt3Co/C cathode electrocatalyst with higher activity and durability than a MEA Pt/C. In the MEA Pt3Co/C, after 5000 ADT-rec (rectangle accelerated durability test) cycles, unlike the MEA Pt/C, there was no oxidation of Pt. In contrast, Co oxidized and dissolved over a wide range of the cathode layer (similar to 70% of the initial Co amount). The larger the size of the cracks and pores in the MEA Pt/C and the smaller the ratio of Pt/ionomer of cracks and pores, the faster the rate of catalyst degradation. In contrast, there was no correlation between the size or Co/ionomer ratio of the cracks and pores and the Co dissolution of the MEA Pt3Co/C. It was shown that Co dissolved in the electrolyte region had an octahedral Co2+-O-6 structure, based on a 150 nm X 150 nm nano-XAFS analysis. It was also shown that its existence suppressed the oxidation and dissolution of Pt. The MEA Pt3Co/C after 10,000 ADT-rec cycles had many cracks and pores in the cathode electrocatalyst layer, and about 90% of Co had been dissolved and removed from the cathode layer. We discovered a metallic Pt-Co alloy band in the electrolyte region of 300-400 nm from the cathode edge and square planar Pt2+-O-4 species and octahedral Co2+-O-6 species in the area between the cathode edge and the Pt-Co band. The transition of Pt and Co chemical species in the Pt3Co/C cathode electrocatalyst in the MEA during the degradation process, as well as a fuel cell deterioration suppression process by Co were visualized for the first time at the nano scale using the same-view nano-XAFS/STEM-EDS combination technique that can measure the MEA under a humid N-2 atmosphere while maintaining the working environment for a fuel cell.
机译:为了获得用于开发下一代聚合物电解质燃料电池的合适的设计政策,我们使用相同视图在老化和降解过程中进行PT和CO物种的可视化分析。纳米X射线吸收精细结构(XAF)/扫描透射电子显微镜(茎) - 能量分散X射线光谱(EDS)技术,我们开发出阐明MEA PT3CO / C阴极电催化剂的耐久性因素和降低机制活动和耐久性而不是MEA PT / C.在MEA PT3CO / C中,在5000 ADT-REC(矩形加速耐久性测试)循环之后,与MEA PT / C不同,没有氧化PT。相反,CO氧化并溶解在宽范围的阴极层(类似于初始CO量的70%)上。 MEA PT / C裂缝和孔的尺寸越大,裂缝和孔的离聚物的比例越小,催化剂降解速率越快。相反,裂缝和孔的尺寸或CO /离聚物与MEA PT3CO / C的共同溶解之间没有相关性。结果表明,基于150nm×150nm纳米XAFS分析,溶解在电解质区域中的CO溶解在电解质区域中具有八面体CO2 + -O-6结构。还表明其存在抑制了Pt的氧化和溶解。在10,000 Adt-REC循环之后的MEA PT3CO / C在阴极电催化剂层中有许多裂缝和孔,并且已经溶解并从阴极层中溶解并除去了约90%的CO。在阴极边缘和方形平面Pt2 + -O-4种和阴极边缘之间的区域中,在电解质区域中的电解质区域中的金属Pt-Co合金带在300-400nm中,在阴极边缘和Pt-之间的区域中的八面体CO2 + -O-6种。 CO乐队。在降解过程中,在MEA中PT3CO / C阴极电催化剂的PT和CO化学物质的转变,以及CO的燃料电池劣化抑制过程首次使用相同的视图纳米在纳米秤上观察到纳米秤-XAFS / STEM-EDS组合技术可以在保持潮湿的N-2气氛下测量MEA,同时保持燃料电池的工作环境。

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