{"title":"多站点协同策略增强高电流密度碱性电解","authors":"Jilong Xu, Haihua Luo, Zhongjie Lai, Zuohuan Chen, Yukun Xiong, Lijuan Zhu, Jiaxiang Lu, Jun Qi, Xiaoning Liu, Leijie Zhang, Yong Han, Hui Zhang, Yifan Ye","doi":"10.1016/j.cej.2025.169782","DOIUrl":null,"url":null,"abstract":"A cost-effective and robust electrocatalyst that can operate at industrial-scale current densities is critical for producing green hydrogen through water splitting. We present a 2D RuCoFeO<sub>x</sub> nanosheet structure, serving as an electrocatalyst for both water splitting and anion-exchange membrane water electrolyzer (AEMWEs) study. The composite material demonstrates outstanding electrochemical performance with acceleration in OER kinetics, enhancement in active surface area, reduced overpotentials, and excellent stability. Based multiple synchrotron radiation techniques and <em>in-situ</em> spectroscopes, we have revealed the electron coupling between Co/Fe and Ru through oxygen-bridge bonding and multi-site cooperative effect. The advanced mapping of resonant Auger spectroscopy (mRAS) effectively differentiates distinct orbital hybridization states, thereby confirming charge transfer between sites. <em>In-situ</em> attenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) and indicates that loaded Ru serve as additional adsorption sites, modulating adsorption of *OOH intermediates. In AEMWEs, the RuCoFeO<sub>x</sub> showcases high activity, achieving 1 A cm<sup>−2</sup> at 1.76 V, and maintains stability at 1 A cm<sup>−2</sup> beyond 700 h. Our investigation offers an insight into the principles of multisite cooperative catalysis and propels the design of highly efficient electrocatalysts for water splitting.","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"35 1","pages":""},"PeriodicalIF":13.2000,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"High current density alkaline water electrolysis enhanced by multi-site cooperative strategy\",\"authors\":\"Jilong Xu, Haihua Luo, Zhongjie Lai, Zuohuan Chen, Yukun Xiong, Lijuan Zhu, Jiaxiang Lu, Jun Qi, Xiaoning Liu, Leijie Zhang, Yong Han, Hui Zhang, Yifan Ye\",\"doi\":\"10.1016/j.cej.2025.169782\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A cost-effective and robust electrocatalyst that can operate at industrial-scale current densities is critical for producing green hydrogen through water splitting. We present a 2D RuCoFeO<sub>x</sub> nanosheet structure, serving as an electrocatalyst for both water splitting and anion-exchange membrane water electrolyzer (AEMWEs) study. The composite material demonstrates outstanding electrochemical performance with acceleration in OER kinetics, enhancement in active surface area, reduced overpotentials, and excellent stability. Based multiple synchrotron radiation techniques and <em>in-situ</em> spectroscopes, we have revealed the electron coupling between Co/Fe and Ru through oxygen-bridge bonding and multi-site cooperative effect. The advanced mapping of resonant Auger spectroscopy (mRAS) effectively differentiates distinct orbital hybridization states, thereby confirming charge transfer between sites. <em>In-situ</em> attenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) and indicates that loaded Ru serve as additional adsorption sites, modulating adsorption of *OOH intermediates. In AEMWEs, the RuCoFeO<sub>x</sub> showcases high activity, achieving 1 A cm<sup>−2</sup> at 1.76 V, and maintains stability at 1 A cm<sup>−2</sup> beyond 700 h. Our investigation offers an insight into the principles of multisite cooperative catalysis and propels the design of highly efficient electrocatalysts for water splitting.\",\"PeriodicalId\":270,\"journal\":{\"name\":\"Chemical Engineering Journal\",\"volume\":\"35 1\",\"pages\":\"\"},\"PeriodicalIF\":13.2000,\"publicationDate\":\"2025-10-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Engineering Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cej.2025.169782\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.cej.2025.169782","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
摘要
一种具有成本效益且坚固耐用的电催化剂,可以在工业规模的电流密度下运行,对于通过水分解生产绿色氢至关重要。我们提出了一种二维RuCoFeOx纳米片结构,作为水分解和阴离子交换膜水电解质(AEMWEs)研究的电催化剂。该复合材料具有OER动力学加速、活性表面积增强、过电位降低和优异的稳定性等优异的电化学性能。基于多重同步辐射技术和原位光谱技术,我们揭示了Co/Fe和Ru之间通过氧桥键和多位点协同效应的电子耦合。共振俄歇光谱(mRAS)的高级映射有效地区分了不同的轨道杂化状态,从而确认了位点之间的电荷转移。原位衰减全反射表面增强红外吸收光谱(ATR-SEIRAS)结果表明,负载Ru作为附加吸附位点,调节*OOH中间体的吸附。在AEMWEs中,RuCoFeOx表现出高活性,在1.76 V时达到1 A cm−2,并且在700 h以上保持1 A cm−2的稳定性。我们的研究提供了对多位点协同催化原理的深入了解,并推动了高效水分解电催化剂的设计。
High current density alkaline water electrolysis enhanced by multi-site cooperative strategy
A cost-effective and robust electrocatalyst that can operate at industrial-scale current densities is critical for producing green hydrogen through water splitting. We present a 2D RuCoFeOx nanosheet structure, serving as an electrocatalyst for both water splitting and anion-exchange membrane water electrolyzer (AEMWEs) study. The composite material demonstrates outstanding electrochemical performance with acceleration in OER kinetics, enhancement in active surface area, reduced overpotentials, and excellent stability. Based multiple synchrotron radiation techniques and in-situ spectroscopes, we have revealed the electron coupling between Co/Fe and Ru through oxygen-bridge bonding and multi-site cooperative effect. The advanced mapping of resonant Auger spectroscopy (mRAS) effectively differentiates distinct orbital hybridization states, thereby confirming charge transfer between sites. In-situ attenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) and indicates that loaded Ru serve as additional adsorption sites, modulating adsorption of *OOH intermediates. In AEMWEs, the RuCoFeOx showcases high activity, achieving 1 A cm−2 at 1.76 V, and maintains stability at 1 A cm−2 beyond 700 h. Our investigation offers an insight into the principles of multisite cooperative catalysis and propels the design of highly efficient electrocatalysts for water splitting.
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.