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

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Xiaoxiao Zhang, Xingyu Zhang, Lan Lin, Junjie Lao, Xin Yao
{"title":"Advancements and Design Strategies for Self-Supported Electrocatalysts Operating in Alkaline Conditions at High-Current-Density","authors":"Xiaoxiao Zhang, Xingyu Zhang, Lan Lin, Junjie Lao, Xin Yao","doi":"10.1021/acsami.5c01897","DOIUrl":null,"url":null,"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.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"43 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.5c01897","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

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.

Abstract Image

高电流密度碱性自负载电催化剂的研究进展与设计策略
碱水裂解是目前最成熟的可持续制氢方法之一。然而,碱性水电解的总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和经济的制氢。虽然学术界在提高电催化剂的活性方面做了大量的努力,但在实现高电流密度下催化剂的高活性和稳定性方面仍然存在挑战。为了解决这一挑战,自支撑型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,然后总结了大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该过程中的优势。随后,本文概述了选择高效、稳定的电催化剂衬底和优化其性能的策略。最后,文章强调了目前裂解水电催化剂从实验室研究向工业应用过渡的瓶颈,指出了未来面临的关键挑战,并对未来的发展方向进行了展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信