无添加镍铁催化剂电沉积过程中电解液 pH 值对电催化 OER 应用的影响

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY
Maximilian Cieluch, Norbert Kazamer, Leonard Böhm, Sebastian Sanden, Swen Zerebecki, Florian Wirkert, Ulf–Peter Apfel, Michael Brodmann
{"title":"无添加镍铁催化剂电沉积过程中电解液 pH 值对电催化 OER 应用的影响","authors":"Maximilian Cieluch,&nbsp;Norbert Kazamer,&nbsp;Leonard Böhm,&nbsp;Sebastian Sanden,&nbsp;Swen Zerebecki,&nbsp;Florian Wirkert,&nbsp;Ulf–Peter Apfel,&nbsp;Michael Brodmann","doi":"10.1002/celc.202400492","DOIUrl":null,"url":null,"abstract":"<p>This study presents the correlation between electrolyte pH, surface morphology, chemical speciation and electro-catalytic oxygen evolution activity of additive-free electrodeposited NiFe catalysts for application in anion exchange membrane water electrolysis. Spherical morphologies were identified at pH 0, shifting towards honey-combed structures at pH 4 with increasing surface area, especially at pH 3. Further, the electrolyte pH was found to influence the NiFe composition and electro-catalytic activity. Enhanced OER activity was noted at pH 2 with overpotentials of 214 mV at 10 mA cm<sup>−2</sup> and 267 mV at 100 mA cm<sup>−2</sup>. The results reveal that the electrolyte pH is a parameter not only influencing the morphology but also tailoring the surface area, Fe oxide and Fe hydroxide composition and consequently the catalytic activity. Further, the outcomes highlight the electrolyte pH as a key process parameter that should be adjusted according to the application, and may substitute the addition of electrolyte-additives, proposing a simpler method for improving catalyst electrodeposition.</p>","PeriodicalId":142,"journal":{"name":"ChemElectroChem","volume":"12 1","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400492","citationCount":"0","resultStr":"{\"title\":\"Effect of Electrolyte pH in Additive-Free NiFe Catalyst Electrodeposition for Electro-Catalytic OER Applications\",\"authors\":\"Maximilian Cieluch,&nbsp;Norbert Kazamer,&nbsp;Leonard Böhm,&nbsp;Sebastian Sanden,&nbsp;Swen Zerebecki,&nbsp;Florian Wirkert,&nbsp;Ulf–Peter Apfel,&nbsp;Michael Brodmann\",\"doi\":\"10.1002/celc.202400492\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>This study presents the correlation between electrolyte pH, surface morphology, chemical speciation and electro-catalytic oxygen evolution activity of additive-free electrodeposited NiFe catalysts for application in anion exchange membrane water electrolysis. Spherical morphologies were identified at pH 0, shifting towards honey-combed structures at pH 4 with increasing surface area, especially at pH 3. Further, the electrolyte pH was found to influence the NiFe composition and electro-catalytic activity. Enhanced OER activity was noted at pH 2 with overpotentials of 214 mV at 10 mA cm<sup>−2</sup> and 267 mV at 100 mA cm<sup>−2</sup>. The results reveal that the electrolyte pH is a parameter not only influencing the morphology but also tailoring the surface area, Fe oxide and Fe hydroxide composition and consequently the catalytic activity. Further, the outcomes highlight the electrolyte pH as a key process parameter that should be adjusted according to the application, and may substitute the addition of electrolyte-additives, proposing a simpler method for improving catalyst electrodeposition.</p>\",\"PeriodicalId\":142,\"journal\":{\"name\":\"ChemElectroChem\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-12-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/celc.202400492\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemElectroChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/celc.202400492\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemElectroChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/celc.202400492","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0

摘要

本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of Electrolyte pH in Additive-Free NiFe Catalyst Electrodeposition for Electro-Catalytic OER Applications

Effect of Electrolyte pH in Additive-Free NiFe Catalyst Electrodeposition for Electro-Catalytic OER Applications

This study presents the correlation between electrolyte pH, surface morphology, chemical speciation and electro-catalytic oxygen evolution activity of additive-free electrodeposited NiFe catalysts for application in anion exchange membrane water electrolysis. Spherical morphologies were identified at pH 0, shifting towards honey-combed structures at pH 4 with increasing surface area, especially at pH 3. Further, the electrolyte pH was found to influence the NiFe composition and electro-catalytic activity. Enhanced OER activity was noted at pH 2 with overpotentials of 214 mV at 10 mA cm−2 and 267 mV at 100 mA cm−2. The results reveal that the electrolyte pH is a parameter not only influencing the morphology but also tailoring the surface area, Fe oxide and Fe hydroxide composition and consequently the catalytic activity. Further, the outcomes highlight the electrolyte pH as a key process parameter that should be adjusted according to the application, and may substitute the addition of electrolyte-additives, proposing a simpler method for improving catalyst electrodeposition.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
×
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