Chloride-resistant seawater electrolysis via hydroxyl network-tailored NiFe hydroxide catalysts on stainless steel

IF 3.5 3区 工程技术 Q2 ENGINEERING, CHEMICAL
AIChE Journal Pub Date : 2025-04-18 DOI:10.1002/aic.18872
Xuanze Wan, Jiankun Li, Linfeng Lei, Jie Wang, Linzhou Zhuang, Zhi Xu
{"title":"Chloride-resistant seawater electrolysis via hydroxyl network-tailored NiFe hydroxide catalysts on stainless steel","authors":"Xuanze Wan, Jiankun Li, Linfeng Lei, Jie Wang, Linzhou Zhuang, Zhi Xu","doi":"10.1002/aic.18872","DOIUrl":null,"url":null,"abstract":"Hydrogen production via seawater electrolysis is limited by chloride corrosion and slow oxygen evolution reaction (OER) kinetics. Here, we present hydroxyl network-engineered NiFe hydroxide catalysts on stainless steel (SS-NiFe-X) via a rapid one-step electrodeposition strategy. During OER, the NiFe hydroxide layer transforms into an active NiFeOOH/NiOOH phase, while <i>in situ</i>-generated surface hydroxyl networks establish hydrogen-bond-mediated pathways that simultaneously enhance OER activity and shield against chloride attack. SS-NiFe-60, with a 500 nm oxide layer, sustains 400 mA cm<sup>−2</sup> for over 500 h in an aggressive chloride environment (1.0 M KOH + 2.0 M NaCl), while the bare SS experiences complete deactivation within 1 h. <i>Operando</i> studies reveal that the hydroxyl network could block chloride penetration by electrostatic repulsion and facilitate OER intermediate adsorption, validated by a membrane electrode assembly electrolyzer stably delivering 250 mA cm<sup>−2</sup> for over 100 h. This scalable design bridges mechanistic insights with industrial seawater electrolysis applications.","PeriodicalId":120,"journal":{"name":"AIChE Journal","volume":"64 1","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"AIChE Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/aic.18872","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Hydrogen production via seawater electrolysis is limited by chloride corrosion and slow oxygen evolution reaction (OER) kinetics. Here, we present hydroxyl network-engineered NiFe hydroxide catalysts on stainless steel (SS-NiFe-X) via a rapid one-step electrodeposition strategy. During OER, the NiFe hydroxide layer transforms into an active NiFeOOH/NiOOH phase, while in situ-generated surface hydroxyl networks establish hydrogen-bond-mediated pathways that simultaneously enhance OER activity and shield against chloride attack. SS-NiFe-60, with a 500 nm oxide layer, sustains 400 mA cm−2 for over 500 h in an aggressive chloride environment (1.0 M KOH + 2.0 M NaCl), while the bare SS experiences complete deactivation within 1 h. Operando studies reveal that the hydroxyl network could block chloride penetration by electrostatic repulsion and facilitate OER intermediate adsorption, validated by a membrane electrode assembly electrolyzer stably delivering 250 mA cm−2 for over 100 h. This scalable design bridges mechanistic insights with industrial seawater electrolysis applications.
耐氯海水电解通过羟基网络定制的NiFe氢氧化物催化剂在不锈钢上
海水电解制氢受到氯离子腐蚀和慢析氧反应动力学的限制。在这里,我们通过快速一步电沉积策略在不锈钢(ss - nfe - x)上提出了羟基网络工程的NiFe氢氧化物催化剂。在OER过程中,NiFe氢氧化物层转变为活性NiFeOOH/NiOOH相,而在原位生成的表面羟基网络建立了氢键介导的途径,同时增强了OER活性并屏蔽了氯化物的攻击。SS- nfe -60具有500 nm的氧化层,在侵略性氯化物环境(1.0 M KOH + 2.0 M NaCl)中维持400 mA cm - 2超过500小时,而裸SS在1小时内完全失活。Operando研究表明,羟基网络可以通过静电排斥阻止氯化物渗透,并促进OER中间吸附,通过膜电极组装电解槽稳定提供250 mA cm - 2超过100小时。这种可扩展的设计将机械见解与工业海水电解应用相结合。
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
AIChE Journal
AIChE Journal 工程技术-工程:化工
CiteScore
7.10
自引率
10.80%
发文量
411
审稿时长
3.6 months
期刊介绍: The AIChE Journal is the premier research monthly in chemical engineering and related fields. This peer-reviewed and broad-based journal reports on the most important and latest technological advances in core areas of chemical engineering as well as in other relevant engineering disciplines. To keep abreast with the progressive outlook of the profession, the Journal has been expanding the scope of its editorial contents to include such fast developing areas as biotechnology, electrochemical engineering, and environmental engineering. The AIChE Journal is indeed the global communications vehicle for the world-renowned researchers to exchange top-notch research findings with one another. Subscribing to the AIChE Journal is like having immediate access to nine topical journals in the field. Articles are categorized according to the following topical areas: Biomolecular Engineering, Bioengineering, Biochemicals, Biofuels, and Food Inorganic Materials: Synthesis and Processing Particle Technology and Fluidization Process Systems Engineering Reaction Engineering, Kinetics and Catalysis Separations: Materials, Devices and Processes Soft Materials: Synthesis, Processing and Products Thermodynamics and Molecular-Scale Phenomena Transport Phenomena and Fluid Mechanics.
×
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