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Performance Enhancement by Adaptation of Long Term Chronoamperometry in Direct Formic Acid Fuel Cell using Palladium Anode Catalyst

机译:通过使用钯阳极催化剂适应长期甲酸安培计在直接甲酸燃料电池中的性能增强

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摘要

In the present study, we suggest a new way to reactivate performance of direct formic acid fuel cell (DFAFC) and explain its mechanism by employing electrochemical analyses like chronoamperometry (CA) and cyclic voltammogram (CV). For the evaluation of DFAFC perforamce, palladium (Pd) and platinum (Pt) are used as anode and cathode catalysts, respectively, and are applied to a Nafion membrane by catalyst-coated membrane spraying. After long DFAFC operation performed at 0.2 and 0.4 V and then CV test, DFAFC performance is better than its initial performance. It is attributed to dissolution of anode Pd into Pd~(2+). By characterizations like TEM, Z-potential, CV and electrochemical impedance spectroscopy, it is evaluated that such dissolved Pd~(2+) ions lead to (1) increase in the electrochemically active surface by reduction in Pd particle size and its improved redistribution and (2) increment in the total oxidation charge by fast reaction rate of the Pd dissolution reaction.
机译:在本研究中,我们提出了一种重新激活直接甲酸燃料电池(DFAFC)性能的新方法,并通过采用计时电流法(CA)和循环伏安法(CV)等电化学分析来解释其机理。为了评估DFAFC的性能,钯(Pd)和铂(Pt)分别用作阳极和阴极催化剂,并通过催化剂涂覆的膜喷涂将其涂覆到Nafion膜上。经过长期的DFAFC操作(在0.2和0.4 V电压下执行),然后进行CV测试,DFAFC性能优于其初始性能。这归因于阳极Pd溶解在Pd〜(2+)中。通过TEM,Z电位,CV和电化学阻抗谱等表征,可以评估出这种溶解的Pd〜(2+)离子通过减小Pd的粒径及其改善的再分布而导致(1)电化学活性表面的增加。 (2)通过Pd溶解反应的快速反应速率增加总氧化电荷。

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