Synergistic Interplay between Fe-based Perovskite Oxides and Co in Electrolyte for Efficient Oxygen Evolution Reaction.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY ChemSusChem Pub Date : 2024-11-11 DOI:10.1002/cssc.202401982
Yuta Inoue, Yuto Miyahara, Kohei Miyazaki, Changhee Lee, Ryo Sakamoto, Takeshi Abe
{"title":"Synergistic Interplay between Fe-based Perovskite Oxides and Co in Electrolyte for Efficient Oxygen Evolution Reaction.","authors":"Yuta Inoue, Yuto Miyahara, Kohei Miyazaki, Changhee Lee, Ryo Sakamoto, Takeshi Abe","doi":"10.1002/cssc.202401982","DOIUrl":null,"url":null,"abstract":"<p><p>Perovskite oxides have been extensively investigated as active electrocatalysts for the oxygen evolution reaction (OER) in alkaline solution. While the OER activity of some perovskite oxides is positively influenced by Fe ions in the electrolyte, the impact of other transition metal ions in the electrolyte remains unclear. In this study, we compared the influence of Co ions intentionally added to the electrolyte on the OER activities of two Fe-based perovskite oxides (Ba0.5Sr0.5FeO3-δ and LaFeO3). While the OER activity of Ba0.5Sr0.5FeO3-δ is significantly enhanced by adding Co ions to the electrolyte, LaFeO3 showed little difference in the OER behavior between the Co-free and Co-containing electrolytes. In the case of Ba0.5Sr0.5FeO3-δ, an amorphous layer was formed, and the Co ions from the electrolyte were incorporated on the surface as a result of OER cycling. On the other hand, Co ions were also detected on the surface of LaFeO3, but its crystalline structure remains unchanged during the OER. Our study suggests that synergistic interplay between the perovskite oxides undergoing a structural transformation at the surface and transition metal ions in the electrolyte can improve the OER activity.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":" ","pages":"e202401982"},"PeriodicalIF":7.5000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cssc.202401982","RegionNum":2,"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

Perovskite oxides have been extensively investigated as active electrocatalysts for the oxygen evolution reaction (OER) in alkaline solution. While the OER activity of some perovskite oxides is positively influenced by Fe ions in the electrolyte, the impact of other transition metal ions in the electrolyte remains unclear. In this study, we compared the influence of Co ions intentionally added to the electrolyte on the OER activities of two Fe-based perovskite oxides (Ba0.5Sr0.5FeO3-δ and LaFeO3). While the OER activity of Ba0.5Sr0.5FeO3-δ is significantly enhanced by adding Co ions to the electrolyte, LaFeO3 showed little difference in the OER behavior between the Co-free and Co-containing electrolytes. In the case of Ba0.5Sr0.5FeO3-δ, an amorphous layer was formed, and the Co ions from the electrolyte were incorporated on the surface as a result of OER cycling. On the other hand, Co ions were also detected on the surface of LaFeO3, but its crystalline structure remains unchanged during the OER. Our study suggests that synergistic interplay between the perovskite oxides undergoing a structural transformation at the surface and transition metal ions in the electrolyte can improve the OER activity.

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
电解质中铁基包晶氧化物与钴的协同作用促进高效氧气进化反应
作为碱性溶液中氧进化反应(OER)的活性电催化剂,人们对透镜氧化物进行了广泛的研究。虽然某些包晶氧化物的 OER 活性受到电解质中铁离子的积极影响,但电解质中其他过渡金属离子的影响仍不清楚。在本研究中,我们比较了有意添加到电解质中的 Co 离子对两种铁基包晶石氧化物(Ba0.5Sr0.5FeO3-δ 和 LaFeO3)的 OER 活性的影响。在电解质中加入 Co 离子后,Ba0.5Sr0.5FeO3-δ 的 OER 活性显著增强,而 LaFeO3 在无 Co 和含 Co 的电解质中的 OER 行为差别不大。对于 Ba0.5Sr0.5FeO3-δ,OER 循环的结果是形成了无定形层,电解质中的 Co 离子融入了表面。另一方面,在 LaFeO3 表面也检测到了 Co 离子,但其晶体结构在 OER 期间保持不变。我们的研究表明,表面发生结构转变的包晶氧化物与电解质中的过渡金属离子之间的协同作用可以提高 OER 活性。
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
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
期刊最新文献
Covalent Organic Frameworks with Regulated Water Adsorption Sites for Efficient Cooling of Electronics. A TEMPO-N3 Complex Enables the Electrochemical C-H Azidation of N-Heterocycles through the Cleavage of Alkoxyamines. PEI-templated ZIF-8 nanoparticles impart the NF membrane with high Mg2+/Li+ separation performance. Green Electrochemical Point-of-Care Devices: Transient Materials and Sustainable Fabrication Methods. Metal-free N, P-Codoped Carbon for Syngas Production with Tunable Composition via CO2 Electrolysis: Addressing the Competition Between CO2 Reduction and H2 Evolution.
×
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:481959085
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