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Model porous electrodes based and carbon nanotubes and organically grafted platinum electrocatalysts allows development of new approaches for the characterization of porous electrodes devoted to fuel cells

机译:基于型多孔电极和碳纳米管和有机接枝的铂电催化剂允许开发用于表征致力于燃料电池的多孔电极的新方法

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This paper reports on the characterization of model porous electrodes based on the combination of organically grafted platinum electrocatalysts and carbon nanotubes. Both, the difficulty to make homogeneous and well controlled deposition of porous electrocatalyts structures on rotating electrodes, and the use of unconventional Platinum Organically Grafted Electrocatalysts (Pt-OGE) lead us to contemplate the development of new approaches for the characterization of the Oxygen Reduction Reaction (ORR) in porous electrode structures. Such developments concern the evaluation of the selectivity of the ORR and the determination of a specific surface area related to the ORR using cyclic voltammetry. For the latter, simple equations established for flat electrodes and planar diffusion are used that describe the peak potential and peak current established as a function of scan speed. The easy manipulation of the organically grafted electrocatalysts allows a controlled combination with carbon nanotubes (CNT) in liquid media. In particular, the coverage density of Pt cores at the carbon nanotube surface can be precisely tuned. The overall process leads to the formation of various porous electrodes structures which consists in the active layer based on Pt-OGE/CNT combinations deposited on a carbon felt. The different electrodes structures are characterized as a function of Platinum loading regarding selectivity and the determination of so the called S-AO2 parameter which the specific surface area of the porous electrodes related to the ORR, expressed in m2/g Pt. The recorded trends exhibit a remarkable consistency for the different porous electrode structures leading to the determination of a feature S-AO2 and catalyst critical loading below which the selectivity is lower than 4. Although additional experimental studies are required to get more insights on these results, the high consistency recorded as a function of catalyst loading suggest that these new approaches might be of particular interest for the determination of feature parameters for a given porous electrode structure devoted to Oxygen Reduction, including non-noble metal electrocatalysts porous based structures.
机译:本上基于有机接枝铂电催化剂和碳纳米管的组合模型多孔电极的表征文件报告。两者的难度,使多孔electrocatalyts结构均匀,很好地控制沉积在旋转电极,并采用非常规的白金有机地嫁接电催化剂(铂OGE)的引导我们去思考的新方法的发展对氧还原反应的表征(ORR)在多孔电极结构。这样的发展涉及ORR的选择性的评价,并与使用循环伏安法的ORR比表面积测定。用于扁平电极和平面扩散确立后者,简单的公式用于描述建立为扫描速度的函数的峰电位和峰电流。的有机接枝电催化剂的易操作允许与碳纳米管(CNT)在液体培养基中的受控组合。特别地,铂的覆盖密度芯在碳纳米管表面可被精确调谐。整个过程导致形成各种多孔电极结构,其包括基于铂 - OGE有源层/沉积在碳毡的CNT的组合。不同电极结构的特征是铂负载的关于选择性和的确定的函数,因此称为S-AO2参数,该参数关系到ORR多孔电极,在2 /克的Pt表示的比表面积。所记录的趋势显示出对于不同的多孔电极结构导致特征S-AO2和催化剂临界载荷的确定,低于该选择性是显着的稠度低于4.虽然附加的实验研究是必需的以获得这些结果进一步的分析,记录为催化剂负载的函数的高稠度表明,这些新的方法可能是的特征参数的确定为专门用于氧还原,包括非贵金属电多孔基础的结构给定的多孔电极结构特别感兴趣的。

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