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有机染料作为燃料电池的催化剂。

Organic dyestuffs as catalysts for fuel cells.

作者信息

Jahnke H, Schönborn M, Zimmermann G

出版信息

Top Curr Chem. 1976;61:133-81. doi: 10.1007/BFb0046059.

Abstract

Electrocatalysis in fuel cells requires as well substances capable of catalyzing the anodic oxidation of fuels as catalysts for the cathodic reduction of oxygen. Several dyestuffs that catalyze oxygen reduction are known, but up to now only one has been described as active in anodic reactions. All these dyestuffs are N4-chelates. Comparative studies have shown that chelates with other types of coordination, in particular N202-, 04-, N2S2- and S4-chelates, are able to catalyze the reduction of oxygen, though they are considerably less active than the N4-compounds. With a given type of coordination, the nature of the central atom has a decisive influence on the catalytic activity of the dyestuff, whereas substitution on the organic skeleton has only a slight effect. Thermal pretreatment of the N4-chelates can considerably increase their stability in electrolytes containing sulfuric acid. All the experimental results point to the conclusion that, with electrocatalysts, as with natural oxygen carriers, the interaction essential for catalysis takes place between the oxygen and the central metal ion. Various assumptions may be made as to the nature of the rate-determining step. The cathodic reduction of oxygen can be regarded as redox catalysis, or it can be considered from the standpoint of molecular orbital theory. The models hitherto suggested for the mechanism of oxygen reduction are tested against the experimental results and a modified model based on MO theory is put forward.

摘要

燃料电池中的电催化既需要能够催化燃料阳极氧化的物质,也需要作为氧阴极还原催化剂的物质。已知有几种染料可催化氧还原,但到目前为止,只有一种被描述为在阳极反应中具有活性。所有这些染料都是N4螯合物。比较研究表明,具有其他类型配位的螯合物,特别是N202-、04-、N2S2-和S4-螯合物,能够催化氧还原,尽管它们的活性比N4化合物低得多。对于给定类型的配位,中心原子的性质对染料的催化活性具有决定性影响,而有机骨架上的取代只有轻微影响。N4螯合物的热预处理可以显著提高它们在含硫酸电解质中的稳定性。所有实验结果都指向这样一个结论:对于电催化剂,就像对于天然氧载体一样,催化所必需的相互作用发生在氧和中心金属离子之间。关于速率决定步骤的性质可以做出各种假设。氧的阴极还原可以被视为氧化还原催化,或者可以从分子轨道理论的角度来考虑。根据实验结果对迄今提出的氧还原机理模型进行了检验,并提出了一种基于分子轨道理论的改进模型。

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