{"title":"Low-Ir-Content Ir0.10Mn0.90O2 Solid Solution for Highly Active Oxygen Evolution in Acid Media","authors":"Hongyan Hu, Shilong Liu, Hongfei Sun, Wenli Sun, Jike Tang, Lingzhi Wei, Xiaowei Chen, Qianwang Chen, Yichao Lin, Ziqi Tian, Jianwei Su","doi":"10.1002/smll.202412096","DOIUrl":null,"url":null,"abstract":"Iridium (Ir)-based materials are the most widely used oxygen evolution reaction (OER) electrocatalysts in proton exchange membrane water electrolysis (PEMWE). However, their commercial application suffers from high cost and insufficient activity. To optimize the atom utilization efficiency of Ir, the aim is to engineer and develop a rutile-structured solid solution catalyst with minimal Ir content, which is identified through a phase boundary. Here, Ir<sub>0.10</sub>Mn<sub>0.90</sub>O<sub>2</sub> represents the lowest Ir content in the desired IrO<sub>2</sub>-MnO<sub>2</sub> solid solution. The Ir<sub>0.10</sub>Mn<sub>0.90</sub>O<sub>2</sub> catalyst exhibits outstanding OER performance in acidic electrolytes, reaching a remarkable mass activity of 1135 A g<sup>−1</sup><sub>Ir</sub> at an overpotential of 300 mV, which is ≈50 times higher than that of a commercial IrO<sub>2</sub> catalyst. Additionally, it demonstrates excellent stability at a current density of 200 mA cm<sup>−2</sup> over 120 h during PEMWE operations. Density functional theory (DFT) calculations indicate that the hydroxylation process can be efficiently promoted by the electron-withdrawing on Ir sites in Ir<sub>0.10</sub>Mn<sub>0.90</sub>O<sub>2</sub>, contributing to the enhancement of OER activity.","PeriodicalId":228,"journal":{"name":"Small","volume":"3 1","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/smll.202412096","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Iridium (Ir)-based materials are the most widely used oxygen evolution reaction (OER) electrocatalysts in proton exchange membrane water electrolysis (PEMWE). However, their commercial application suffers from high cost and insufficient activity. To optimize the atom utilization efficiency of Ir, the aim is to engineer and develop a rutile-structured solid solution catalyst with minimal Ir content, which is identified through a phase boundary. Here, Ir0.10Mn0.90O2 represents the lowest Ir content in the desired IrO2-MnO2 solid solution. The Ir0.10Mn0.90O2 catalyst exhibits outstanding OER performance in acidic electrolytes, reaching a remarkable mass activity of 1135 A g−1Ir at an overpotential of 300 mV, which is ≈50 times higher than that of a commercial IrO2 catalyst. Additionally, it demonstrates excellent stability at a current density of 200 mA cm−2 over 120 h during PEMWE operations. Density functional theory (DFT) calculations indicate that the hydroxylation process can be efficiently promoted by the electron-withdrawing on Ir sites in Ir0.10Mn0.90O2, contributing to the enhancement of OER activity.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.