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Fuel blends: Enhanced electro-oxidation of formic acid in its blend with methanol at platinum nanoparticles modified glassy carbon electrodes

机译:燃料混合物:在铂纳米颗粒修饰的玻碳电极上,甲酸与甲醇的混合物增强了电氧化作用

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摘要

The current study addresses, for the first time, the enhanced direct electro-oxidation of formic acid (FA) at platinum-nanoparticles modified glassy carbon (nano-Pt/GC) electrode in the presence of methanol (Me0H) as a blending fuel. This enhancement is probed by: (i) the increase of the direct oxidation current of FA to CO2 (I-p(d), dehydrogenation pathway), (ii) suppressing the dehydration pathway (I-p(ind), producing the poisoning intermediate CO) and (iii) a favorable negative shift of the onset potential of I-p(d) with increasing the mole fraction of MeOH in the blend. Furthermore, the charge of the direct FA oxidation in 0.3 M FA + 0.3 M MeOH blend is by 14 and 21 times higher than that observed for 0.3 M FA and 0.3 M MeOH, respectively. MeOH is believed to adsorb at the Pt surface sites and thus disfavor the "nonfaradaic" dissociation of FA (which produces the poisoning CO intermediate), i.e., MeOH induces a high CO tolerance of the Pt catalyst. The enhanced oxidation activity indicates that FA/MeOH blend is a promising fuel system. (C) 2015 Elsevier B.V. All rights reserved.
机译:当前的研究首次解决了在甲醇(MeOH)作为混合燃料存在下,铂-纳米粒子改性玻璃碳(nano-Pt / GC)电极上甲酸(FA)的增强的直接电氧化作用。可以通过以下方式探究这种增强:(i)FA对CO2的直接氧化电流增加(Ip(d),脱氢途径),(ii)抑制脱水途径(Ip(ind),产生中毒中间体CO)和(iii)随着混合物中MeOH的摩尔分数的增加,Ip(d)的起始电势的有利的负位移。此外,在0.3 M FA + 0.3 M MeOH混合物中直接FA氧化的电荷分别比在0.3 M FA和0.3 M MeOH中观察到的电荷高14和21倍。据信MeOH吸附在Pt表面部位,因此不利于FA的“非法拉第”解离(其产生中毒的CO中间体),即,MeOH引起Pt催化剂的高CO耐受性。增强的氧化活性表明FA / MeOH混合物是一种有前途的燃料系统。 (C)2015 Elsevier B.V.保留所有权利。

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