Strategic Engineering of Axially Coordinated Ligands in Fe-N-C Catalysts for Enhanced Oxygen Reduction Electrocatalysis.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2025-05-28 DOI:10.1002/cssc.202500855
Zongxuan Yang, Qingchen Wu, Hongwei Zhang, Cejun Hu, Xiaojun Bao, Pei Yuan
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引用次数: 0

Abstract

The single-atom Fe-N-C electrocatalyst is considered one of the most promising alternatives to the expensive and scarce Pt-based catalysts for promoting oxygen reduction reaction (ORR) in fuel cells. Regulating the coordination environment of the Fe center is a feasible strategy to improve its stability and catalytic activity. Recently, the introduction of axial ligands to Fe-N-C has attracted extensive research interest, providing a new dimension for coordination environment regulation compared with the common approaches of in-plane doping or defect construction. This review focuses on discussing the contribution of axial ligands decoration to the activity and stability of the Fe-N-C catalyst, evaluating different types of axial ligands that have been introduced in recent literature. Through summarizing the progress in decorating axial ligands to the Fe-N-C system, this review provides profound insights for the design and preparation of axially coordinated Fe-N-C catalysts.

Fe-N-C催化剂轴向配体增强氧还原电催化的策略工程。
单原子Fe-N-C电催化剂被认为是燃料电池中促进氧还原反应(ORR)的最有前途的替代昂贵而稀缺的pt基催化剂之一。调节铁中心的配位环境是提高其稳定性和催化活性的可行策略。近年来,向Fe-N-C中引入轴向配体引起了广泛的研究兴趣,与平面内掺杂或缺陷构建的常见方法相比,它为配位环境调节提供了一个新的维度。本文主要讨论了轴向配体修饰对Fe-N-C催化剂活性和稳定性的贡献,并对近年来文献中介绍的不同类型的轴向配体进行了评价。本文综述了轴向配体修饰Fe-N-C体系的研究进展,为轴向配位Fe-N-C催化剂的设计和制备提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
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