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Transport behaviour of Cl- in composite films of polypyrrole and CoFe2O4 obtained for oxygen reduction

机译:Cl-在聚吡咯与CoFe2O4复合膜中的输运行为

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Electrodeposited films of polypyrrole (PPy) and composite of PPy and CoFe2O4 nanoparticles, incorporated with a charge compensating electrolyte anion (Cl-) are obtained on polished and pretreated graphite electrodes. Electrochemical investigations of these electronically conductive films carried out in a 0.8 mol dm(-3) KCl + 5.0 mmol dm(-3) KOH solution show that incorporation of oxide nanoparticles decreases porosity of the polymer matrix. The average apparent diffusion coefficient (D-a) value of dopant (Cl-) is observed to be approximately 3 times higher in a pure PPy-film compared to composite one. The sum of the film and solution resistances, though higher with the composite electrode, remained practically constant under cathodic polarization conditions. In contrast to a non-composite electrode of the same oxide, the composite electrode exhibited much better electrocatalytic activity and remarkable stability for O-2 reduction reaction (ORR).
机译:在抛光和预处理的石墨电极上获得了聚吡咯(PPy)以及PPy和CoFe2O4纳米颗粒复合物的电沉积膜,并结合了电荷补偿电解质阴离子(Cl-)。在0.8 mol dm(-3)KCl + 5.0 mmol dm(-3)KOH溶液中进行的这些导电膜的电化学研究表明,掺入氧化物纳米颗粒会降低聚合物基质的孔隙率。与纯复合材料相比,纯PPy膜的掺杂剂(Cl-)的平均表观扩散系数(D-a)值大约高3倍。膜电阻和溶液电阻的总和,尽管对于复合电极而言更高,但在阴极极化条件下实际上保持恒定。与相同氧化物的非复合电极相比,该复合电极表现出更好的电催化活性和对O-2还原反应(ORR)的显着稳定性。

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