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结合标度关系克服了氧分子电催化中速率与过电位之间的权衡。

Combining scaling relationships overcomes rate versus overpotential trade-offs in O molecular electrocatalysis.

作者信息

Martin Daniel J, Mercado Brandon Q, Mayer James M

机构信息

Yale University, Department of Chemistry, New Haven, CT, USA.

出版信息

Sci Adv. 2020 Mar 13;6(11):eaaz3318. doi: 10.1126/sciadv.aaz3318. eCollection 2020 Mar.

Abstract

The development of advanced chemical-to-electrical energy conversions requires fast and efficient electrocatalysis of multielectron/multiproton reactions, such as the oxygen reduction reaction (ORR). Using molecular catalysts, correlations between the reaction rate and energy efficiency have recently been identified. Improved catalysis requires circumventing the rate versus overpotential trade-offs implied by such "scaling relationships." Described here is an ORR system-using a soluble iron porphyrin and weak acids-with the best reported combination of rate and efficiency for a soluble ORR catalyst. This advance is achieved not by "breaking" scaling relationships but rather by combining two of them. Key to this behavior is a polycationic ligand, which enhances anionic ligand binding and changes the catalyst . These results show how combining scaling relationships is a powerful way toward improved electrocatalysis.

摘要

先进的化学能到电能转换的发展需要对多电子/多质子反应进行快速高效的电催化,比如氧还原反应(ORR)。利用分子催化剂,最近已经确定了反应速率与能量效率之间的相关性。改进催化作用需要规避此类“比例关系”所隐含的速率与过电位之间的权衡。本文描述了一种ORR体系——使用可溶性铁卟啉和弱酸——具有可溶性ORR催化剂所报道的最佳速率与效率组合。这一进展并非通过“打破”比例关系实现,而是通过将其中两个关系相结合来达成。这种行为的关键在于一种聚阳离子配体,它增强了阴离子配体的结合并改变了催化剂。这些结果表明,结合比例关系是实现改进电催化的有力途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc4a/7069693/34316a74f975/aaz3318-F1.jpg

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