{"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.
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。
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