Development of Ternary Layered Double Hydroxide Oxygen Evolution Reaction Electrocatalyst for Anion Exchange Membrane Water Electrolysis

IF 17.7 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Accounts of Chemical Research Pub Date : 2024-06-05 DOI:10.3365/kjmm.2024.62.6.472
Shin-Woo Myeong, Song Jin, Chi-Kwan Kim, Jooyoung Lee, Yangdo Kim, Mook Choi
{"title":"Development of Ternary Layered Double Hydroxide Oxygen Evolution Reaction Electrocatalyst for Anion Exchange Membrane Water Electrolysis","authors":"Shin-Woo Myeong, Song Jin, Chi-Kwan Kim, Jooyoung Lee, Yangdo Kim, Mook Choi","doi":"10.3365/kjmm.2024.62.6.472","DOIUrl":null,"url":null,"abstract":"To achieve net zero emissions, green hydrogen should be produced via water electrolysis with renewable energy. To develop efficient anion exchange membrane water electrolyzers (AEMWE), the development of efficient and stable non-precious metal electrocatalysts for the oxygen evolution reaction (OER) is essential. In this study, a high-performance ternary NiFeCo-layer double hydroxide (LDH) electrocatalyst for AEMWE was easily developed by the co-precipitation method. The introduction of Co has been shown to have an effect on the electronic structure of Ni and Fe, improving their intrinsic OER properties. In addition, the three-dimensional flower-like nanosheet morphology improved mass transfer and achieved excellent current density at high voltages. The ternary NiFeCo-LDH electrocatalyst requires low overpotentials (253 mV at 10 mA cm-2) and Tafel slope (45 mV dec-1) in 1 M KOH. AEMWE using the ternary NiFeCo-LDH electrocatalyst showed excellent electrolysis performance with a high current density of 2.27 A cm-2 at 1.8 V cell. Moreover, an energy conversion efficiency of 86.73 % was achieved during the durability test for 100 hours at a current density of 0.5 A cm-2. The performance of the AEMWE electrolyzer utilizing the ternary NiFeCo-LDH electrocatalyst surpassed that of previously reported AEMWE electrolyzers. This work reports a highly active OER electrocatalyst that could open numerous opportunities for the development of ternary LDH electrocatalysts in AEMWE.","PeriodicalId":1,"journal":{"name":"Accounts of Chemical Research","volume":"3 5","pages":""},"PeriodicalIF":17.7000,"publicationDate":"2024-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Accounts of Chemical Research","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.3365/kjmm.2024.62.6.472","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

To achieve net zero emissions, green hydrogen should be produced via water electrolysis with renewable energy. To develop efficient anion exchange membrane water electrolyzers (AEMWE), the development of efficient and stable non-precious metal electrocatalysts for the oxygen evolution reaction (OER) is essential. In this study, a high-performance ternary NiFeCo-layer double hydroxide (LDH) electrocatalyst for AEMWE was easily developed by the co-precipitation method. The introduction of Co has been shown to have an effect on the electronic structure of Ni and Fe, improving their intrinsic OER properties. In addition, the three-dimensional flower-like nanosheet morphology improved mass transfer and achieved excellent current density at high voltages. The ternary NiFeCo-LDH electrocatalyst requires low overpotentials (253 mV at 10 mA cm-2) and Tafel slope (45 mV dec-1) in 1 M KOH. AEMWE using the ternary NiFeCo-LDH electrocatalyst showed excellent electrolysis performance with a high current density of 2.27 A cm-2 at 1.8 V cell. Moreover, an energy conversion efficiency of 86.73 % was achieved during the durability test for 100 hours at a current density of 0.5 A cm-2. The performance of the AEMWE electrolyzer utilizing the ternary NiFeCo-LDH electrocatalyst surpassed that of previously reported AEMWE electrolyzers. This work reports a highly active OER electrocatalyst that could open numerous opportunities for the development of ternary LDH electrocatalysts in AEMWE.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
开发用于阴离子交换膜水电解的三元层状双氢氧根进氧反应电催化剂
为实现净零排放,应利用可再生能源通过电解水生产绿色氢气。要开发高效的阴离子交换膜水电解槽(AEMWE),开发高效稳定的非贵金属氧进化反应(OER)电催化剂至关重要。在本研究中,通过共沉淀法轻松开发出了用于 AEMWE 的高性能三元镍铁钴层双氢氧化物(LDH)电催化剂。研究表明,Co 的引入会对 Ni 和 Fe 的电子结构产生影响,从而改善它们的内在 OER 性能。此外,三维花朵状纳米片形态改善了传质,并在高电压下实现了出色的电流密度。三元 NiFeCo-LDH 电催化剂在 1 M KOH 中需要较低的过电位(10 mA cm-2 时为 253 mV)和 Tafel 斜坡(45 mV dec-1)。使用三元镍铁合金-LDH 电催化剂的 AEMWE 显示出卓越的电解性能,在 1.8 V 的电池中电流密度高达 2.27 A cm-2。此外,在电流密度为 0.5 A cm-2 的条件下,经过 100 小时的耐久性测试,能量转换效率达到了 86.73%。利用三元 NiFeCo-LDH 电催化剂的 AEMWE 电解槽的性能超过了之前报道的 AEMWE 电解槽。这项工作报告了一种高活性 OER 电催化剂,它为在 AEMWE 中开发三元 LDH 电催化剂提供了许多机会。
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 去求助
来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
期刊最新文献
Conjugated Oligoelectrolytes as Optical Probes. Charge State Evolution in Electrocatalysts for Bridging the Activity-Stability Gap in Acidic Oxygen Evolution. Computational and AI-Driven Ecosystem for Structure-Based Covalent Drug Discovery. Metabolic RNA Labeling-Enabled Time-Resolved Single-Cell RNA Sequencing. Multifunctional Guest-Hosting Triple-Stranded Helicates: From Anion Recognition to Quantum Information Applications.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1