Zhi Wang , Jinpeng Li , Chengdeng Wang , Jiashuai Wang , Xiangrui Chen , Jun Wu , Zhiming Bai , Yan Gao , Li Chen , Xiaoqin Yan
{"title":"Ce doping induces lattice expansion of cobalt oxide electrocatalyst to achieve efficient proton exchange membrane water electrolysis","authors":"Zhi Wang , Jinpeng Li , Chengdeng Wang , Jiashuai Wang , Xiangrui Chen , Jun Wu , Zhiming Bai , Yan Gao , Li Chen , Xiaoqin Yan","doi":"10.1016/j.mtphys.2024.101641","DOIUrl":null,"url":null,"abstract":"<div><div>The development of non-precious metal anode catalysts with high performance and low cost for proton exchange membrane (PEM) water electrolysis presents a significant challenge. This work successfully synthesized a bimetallic-doped cobalt-based oxide titanium diboride composite structure catalyst (Ce-Mn-Co<sub>3</sub>O<sub>4</sub>/TiB<sub>2</sub>) by combining hydrothermal methods with heat treatment processes. Ce doping induces surface oxygen vacancies of Co<sub>3</sub>O<sub>4</sub> to optimize adsorption energy, while Mn stabilizes lattice oxygen and impedes the dissolution of metal ions. Theoretical simulations support the experimental results, highlighting the strain effect of Ce doping on the Co<sub>3</sub>O<sub>4</sub>-TiB<sub>2</sub> interface, promoting further charge redistribution, and enhancing catalyst conductivity. Ce-Mn-Co<sub>3</sub>O<sub>4</sub>/TiB<sub>2</sub> exhibits a low oxygen evolution overpotential (389 mV @10 mA/cm<sup>2</sup>). Upon assembly into a PEM electrolytic cell, it achieves a current density of 250 mA/cm<sup>2</sup> at 1.63 V and demonstrates stable operation for nearly 25 h. This research provides novel ideas and methodologies for developing non-precious metal OER electrocatalysts suitable for PEM electrolysis.</div></div>","PeriodicalId":18253,"journal":{"name":"Materials Today Physics","volume":"51 ","pages":"Article 101641"},"PeriodicalIF":10.0000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Today Physics","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2542529324003171","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The development of non-precious metal anode catalysts with high performance and low cost for proton exchange membrane (PEM) water electrolysis presents a significant challenge. This work successfully synthesized a bimetallic-doped cobalt-based oxide titanium diboride composite structure catalyst (Ce-Mn-Co3O4/TiB2) by combining hydrothermal methods with heat treatment processes. Ce doping induces surface oxygen vacancies of Co3O4 to optimize adsorption energy, while Mn stabilizes lattice oxygen and impedes the dissolution of metal ions. Theoretical simulations support the experimental results, highlighting the strain effect of Ce doping on the Co3O4-TiB2 interface, promoting further charge redistribution, and enhancing catalyst conductivity. Ce-Mn-Co3O4/TiB2 exhibits a low oxygen evolution overpotential (389 mV @10 mA/cm2). Upon assembly into a PEM electrolytic cell, it achieves a current density of 250 mA/cm2 at 1.63 V and demonstrates stable operation for nearly 25 h. This research provides novel ideas and methodologies for developing non-precious metal OER electrocatalysts suitable for PEM electrolysis.
期刊介绍:
Materials Today Physics is a multi-disciplinary journal focused on the physics of materials, encompassing both the physical properties and materials synthesis. Operating at the interface of physics and materials science, this journal covers one of the largest and most dynamic fields within physical science. The forefront research in materials physics is driving advancements in new materials, uncovering new physics, and fostering novel applications at an unprecedented pace.