Atomically Dispersed Metal Catalysts for Oxygen Reduction Reaction: Two‐Electron vs. Four‐Electron Pathways

IF 16.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Ao Yu, Yang Yang
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引用次数: 0

Abstract

Developing eco‐friendly electrochemical devices for electrosynthesis, fuel cells (FCs), and metal‐air batteries (MABs) requires precisely designing the electronic pathway in the oxygen reduction reaction (ORR) process. Understanding the principle of designing low‐cost, highly active, and stable catalysts helps to reduce the usage of noble metals in ORR. Atomically dispersed metal catalysts (ADMCs) emerge as promising alternatives to replace commercial noble metals due to their high utilization of active metal atoms, high intrinsic activity, and controllable coordination environments. In this review, the research tendency and reaction mechanisms in ORR are first summarized. The basic principles concerning the geometric size of the catalysts for both two‐electron ORR (2e ORR) and four‐electron ORR (4e ORR) were then discussed, aiming to outline the material design differences for 2e ORR and 4e ORR. Subsequently, the recent advances concentrated on the ADMCs, including coordination numbers, light heteroatom doping, dual‐metal atoms‐based coordination, and interaction between nanoparticle (NPs)/nanoclusters (NCs) and ADMs are documented. Finally, the key challenges and opportunities in the future design of ADMCs for the ORR are highlighted.
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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