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用于在高电流密度碱性条件下运行的自支撑电催化剂的进展与设计策略

Advancements and Design Strategies for Self-Supported Electrocatalysts Operating in Alkaline Conditions at High-Current-Density.

作者信息

Zhang Xiaoxiao, Zhang Xingyu, Lin Lan, Lao Junjie, Yao Xin

机构信息

Binzhou Institute of Technology, Binzhou 256606, China.

School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

ACS Appl Mater Interfaces. 2025 Jun 18;17(24):34872-34891. doi: 10.1021/acsami.5c01897. Epub 2025 Jun 5.

Abstract

Alkaline water splitting is one of the most mature sustainable hydrogen production methods. However, the overall efficiency of alkaline water electrolysis is significantly constrained by the anode oxygen evolution reaction, where the four-electron transfer process leads to slow reaction kinetics, limiting the achievement of efficient and cost-effective hydrogen production at high-current-density. Although substantial efforts have been made in the academic community to enhance the activity of electrocatalysts, challenges remain in achieving high activity and stability of catalysts at high-current-density. To address this challenge, self-supported transition metal catalysts have attracted increasing attention due to their high conductivity and structural stability. This paper first introduces the basic principles of water electrolysis from a thermodynamic perspective, then summarizes the main challenges faced by water electrolysis catalysts at high-current-density, and discusses the advantages of self-supported electrodes in this process. Subsequently, the paper outlines strategies for selecting efficient and stable electrocatalyst substrates and optimizing their performance. Finally, the article highlights the current bottlenecks in the transition of water-splitting electrocatalysts from laboratory research to industrial applications, identifies key challenges for the future, and provides an outlook on future development directions.

摘要

碱性水分解是最成熟的可持续制氢方法之一。然而,碱性水电解的整体效率受到阳极析氧反应的显著限制,其中四电子转移过程导致反应动力学缓慢,限制了在高电流密度下实现高效且经济高效的制氢。尽管学术界已做出大量努力来提高电催化剂的活性,但在高电流密度下实现催化剂的高活性和稳定性仍面临挑战。为应对这一挑战,自支撑过渡金属催化剂因其高导电性和结构稳定性而受到越来越多的关注。本文首先从热力学角度介绍了水电解的基本原理,然后总结了高电流密度下水电解催化剂面临的主要挑战,并讨论了自支撑电极在此过程中的优势。随后,本文概述了选择高效稳定的电催化剂基底并优化其性能的策略。最后,文章强调了水分解电催化剂从实验室研究向工业应用转变过程中的当前瓶颈,确定了未来的关键挑战,并展望了未来的发展方向。

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