Pt和非Pt表面氧还原电催化的基本机理:酸性与碱性介质

N. Ramaswamy, S. Mukerjee
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引用次数: 320

摘要

复杂的电化学反应,如氧还原反应(ORR)涉及多电子转移是一个电催化球内电子转移过程,表现出强烈的依赖于电极表面的性质。这一标准(以及在酸性电解质中所需的稳定性)在很大程度上限制了ORR催化剂的铂基表面。本文讨论了碱性介质中的新证据,阐明了表面无关的外球电子转移组分在整个电催化过程中的作用。这种表面非特异性使得在碱性介质中使用广泛的非贵金属表面作为ORR电极材料成为可能。然而,这个外球过程主要只导致过氧化物中间体作为最终产品。利用热解金属卟啉作为电催化剂,强调了通过促进分子氧在活性位点的直接吸附来促进电催化球内电子转移的重要性。比较了酸性和碱性条件下ORR的反应机理。在碱性介质中进行ORR的主要优点是活性位点上过氧化氢中间体的活化增强,从而实现完整的四电子转移。提出了包含外球和内球电子转移机制的ORR反应方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fundamental Mechanistic Understanding of Electrocatalysis of Oxygen Reduction on Pt and Non-Pt Surfaces: Acid versus Alkaline Media
Complex electrochemical reactions such as Oxygen Reduction Reaction (ORR) involving multi-electron transfer is an electrocatalytic inner-sphere electron transfer process that exhibit strong dependence on the nature of the electrode surface. This criterion (along with required stability in acidic electrolytes) has largely limited ORR catalysts to the platinum-based surfaces. New evidence in alkaline media, discussed here, throws light on the involvement of surface-independent outer-sphere electron transfer component in the overall electrocatalytic process. This surface non-specificity gives rise to the possibility of using a wide-range of non-noble metal surfaces as electrode materials for ORR in alkaline media. However, this outer-sphere process predominantly leads only to peroxide intermediate as the final product. The importance of promoting the electrocatalytic inner-sphere electron transfer by facilitation of direct adsorption of molecular oxygen on the active site is emphasized by using pyrolyzed metal porphyrins as electrocatalysts. A comparison of ORR reaction mechanisms between acidic and alkaline conditions is elucidated here. The primary advantage of performing ORR in alkaline media is found to be the enhanced activation of the peroxide intermediate on the active site that enables the complete four-electron transfer. ORR reaction schemes involving both outer- and inner-sphere electron transfer mechanisms are proposed.
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