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首页> 外文期刊>Electrochimica Acta >Determination of selectivity and specific area related to oxygen reduction reaction as a function of catalyst loading on non-noble metal based electrocatalyst porous electrodes: an example on nitrogen doped carbon nanotube
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Determination of selectivity and specific area related to oxygen reduction reaction as a function of catalyst loading on non-noble metal based electrocatalyst porous electrodes: an example on nitrogen doped carbon nanotube

机译:与基于非贵金属基电催化剂多孔电极上催化剂负载量的氧还原反应有关的选择性和比表面积的确定:以氮掺杂碳纳米管为例

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In a recent paper, model porous electrodes based on carbon nanotube and platinum organically grafted electrocatalysts were used to establish the determination of a specific surface area related to oxygen reduction reaction (ORR) in HClO4 1 M, using cyclic voltammetry as a function of scan speed. Identical behavior was found for the trends of this parameter called S-AO(2) and the selectivity of the ORR as a function of catalyst loading, for different model porous electrode structures. In the present paper, we report such a study on porous electrodes based on non-noble metal electrocatalysts built from nitrogen doped carbon nanotubes (N-CNT). The trends observed for S-AO(2) and the selectivity of the ORR as a function of N-CNT loading are exactly the same as those observed for model porous electrodes. This suggests the interest of these approaches and in particular the determination of the S-AO(2) parameter for the comparison of potentialities of different non-noble electrocatalysts, for example based on nitrogen doped carbon structures towards the ORR. Indeed, although the amount of chemical species supposed to be responsible for the ORR can be estimated using various methods, their accessibility at the level of the nano-object itself and more globally in the porous structure of an active layer is essentially unknown. The S-AO(2) parameter value is presumably directly related to the active sites which are accessible to the oxygen reduction in a porous structure. (C) 2014 Elsevier Ltd. All rights reserved.
机译:在最近的论文中,使用循环伏安法作为扫描速度的函数,使用基于碳纳米管和铂有机接枝的电催化剂的模型多孔电极来确定与HClO4 1 M中的氧还原反应(ORR)相关的比表面积。 。对于不同模型的多孔电极结构,发现了该参数S-AO(2)的趋势和ORR的选择性与催化剂负载的函数相同的行为。在本论文中,我们报告了对基于由氮掺杂碳纳米管(N-CNT)构建的非贵金属电催化剂的多孔电极的研究。观察到的S-AO(2)趋势和ORR选择性随N-CNT负载变化的趋势与模型多孔电极观察到的趋势完全相同。这表明了这些方法的兴趣,尤其是确定S-AO(2)参数以比较不同的非贵金属电催化剂的电势,例如基于朝向ORR的氮掺杂碳结构。确实,尽管可以使用各种方法来估计负责ORR的化学物种的数量,但是在纳米物体本身的水平以及更广泛地在活性层的多孔结构中它们的可及性基本上是未知的。 S-AO(2)参数值可能直接与多孔结构中的氧还原可接近的活性位有关。 (C)2014 Elsevier Ltd.保留所有权利。

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