Yu Zhang, Qiang Wan, Liqiu Huang, Tao Jiang, Shixin Wu, Derun Li, Yichao Liu, Hengyi Wu and Feng Ren
{"title":"双功能高熵合金电催化剂在工业水平电流密度下稳定的整体水分解","authors":"Yu Zhang, Qiang Wan, Liqiu Huang, Tao Jiang, Shixin Wu, Derun Li, Yichao Liu, Hengyi Wu and Feng Ren","doi":"10.1039/D5TA02103K","DOIUrl":null,"url":null,"abstract":"<p >High-entropy materials offer a wide range of potential applications in the catalysis domain due to their multi-active site characteristics and cocktail effect. However, the development of bifunctional electrocatalysts with both superior efficiency and excellent stability under both industrial preparation and industrial running conditions remains a significant challenge. Herein, a scalable plasma spraying strategy is developed to fabricate FeCoNiCrMn HEA catalysts with multimetal synergy, enabling robust bifunctional activity for oxygen and hydrogen evolution reactions (OER/HER). The HEA exhibits ultralow overpotentials of 220 mV (OER) and 69 mV (HER) at 10 mA cm<small><sup>−2</sup></small>, alongside exceptional durability over 1000 h (OER) and 500 h (HER) at 1000 mA cm<small><sup>−2</sup></small>. In an anion exchange membrane water electrolyzer (AEMWE), the HEA achieves 1000 mA cm<small><sup>−2</sup></small> at merely 2.18 V, outperforming commercial Ni mesh (3.40 V) and Raney Ni (3.03 V) electrode systems. Crucially, stable operation for 200 h at 1000 mA cm<small><sup>−2</sup></small> under industrial conditions (1 M KOH, 80 °C) demonstrates the viability of scalable HEA catalysts for practical water splitting. This work bridges the gap between lab-scale innovation and industrial electrocatalyst deployment, offering a promising pathway for large-scale hydrogen production.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":" 23","pages":" 17384-17392"},"PeriodicalIF":9.5000,"publicationDate":"2025-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bifunctional high-entropy alloy electrocatalysts for stable overall water splitting at industrial-level current densities†\",\"authors\":\"Yu Zhang, Qiang Wan, Liqiu Huang, Tao Jiang, Shixin Wu, Derun Li, Yichao Liu, Hengyi Wu and Feng Ren\",\"doi\":\"10.1039/D5TA02103K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >High-entropy materials offer a wide range of potential applications in the catalysis domain due to their multi-active site characteristics and cocktail effect. However, the development of bifunctional electrocatalysts with both superior efficiency and excellent stability under both industrial preparation and industrial running conditions remains a significant challenge. Herein, a scalable plasma spraying strategy is developed to fabricate FeCoNiCrMn HEA catalysts with multimetal synergy, enabling robust bifunctional activity for oxygen and hydrogen evolution reactions (OER/HER). The HEA exhibits ultralow overpotentials of 220 mV (OER) and 69 mV (HER) at 10 mA cm<small><sup>−2</sup></small>, alongside exceptional durability over 1000 h (OER) and 500 h (HER) at 1000 mA cm<small><sup>−2</sup></small>. In an anion exchange membrane water electrolyzer (AEMWE), the HEA achieves 1000 mA cm<small><sup>−2</sup></small> at merely 2.18 V, outperforming commercial Ni mesh (3.40 V) and Raney Ni (3.03 V) electrode systems. Crucially, stable operation for 200 h at 1000 mA cm<small><sup>−2</sup></small> under industrial conditions (1 M KOH, 80 °C) demonstrates the viability of scalable HEA catalysts for practical water splitting. This work bridges the gap between lab-scale innovation and industrial electrocatalyst deployment, offering a promising pathway for large-scale hydrogen production.</p>\",\"PeriodicalId\":82,\"journal\":{\"name\":\"Journal of Materials Chemistry A\",\"volume\":\" 23\",\"pages\":\" 17384-17392\"},\"PeriodicalIF\":9.5000,\"publicationDate\":\"2025-05-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Chemistry A\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/ta/d5ta02103k\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ta/d5ta02103k","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
高熵材料以其多活性位点特性和鸡尾酒效应在催化领域具有广泛的应用前景。然而,开发在工业制备和工业运行条件下都具有优异效率和稳定性的双功能电催化剂仍然是一个重大挑战。本研究开发了一种可扩展的等离子喷涂策略,用于制造具有多金属协同作用的FeCoNiCrMn HEA催化剂,使氧和氢的析出反应(OER/HER)具有强大的双功能活性。HEA在10 mA cm - 2下具有220 mV (OER)和69 mV (HER)的超低过电位,在1000 mA cm - 2下具有超过1000 h (OER)和500 h (HER)的优异耐久性。在阴离子交换膜水电解槽(AEMWE)中,HEA仅在2.18 V下即可达到1000 mA cm - 2,优于商用Ni mesh (3.40 V)和Raney Ni (3.03 V)电极系统。关键是,在工业条件下(1 M KOH, 80°C),在1000 mA cm−2下稳定运行200小时,证明了可扩展HEA催化剂在实际水分解中的可行性。这项工作弥合了实验室规模创新和工业电催化剂部署之间的差距,为大规模制氢提供了一条有希望的途径。
Bifunctional high-entropy alloy electrocatalysts for stable overall water splitting at industrial-level current densities†
High-entropy materials offer a wide range of potential applications in the catalysis domain due to their multi-active site characteristics and cocktail effect. However, the development of bifunctional electrocatalysts with both superior efficiency and excellent stability under both industrial preparation and industrial running conditions remains a significant challenge. Herein, a scalable plasma spraying strategy is developed to fabricate FeCoNiCrMn HEA catalysts with multimetal synergy, enabling robust bifunctional activity for oxygen and hydrogen evolution reactions (OER/HER). The HEA exhibits ultralow overpotentials of 220 mV (OER) and 69 mV (HER) at 10 mA cm−2, alongside exceptional durability over 1000 h (OER) and 500 h (HER) at 1000 mA cm−2. In an anion exchange membrane water electrolyzer (AEMWE), the HEA achieves 1000 mA cm−2 at merely 2.18 V, outperforming commercial Ni mesh (3.40 V) and Raney Ni (3.03 V) electrode systems. Crucially, stable operation for 200 h at 1000 mA cm−2 under industrial conditions (1 M KOH, 80 °C) demonstrates the viability of scalable HEA catalysts for practical water splitting. This work bridges the gap between lab-scale innovation and industrial electrocatalyst deployment, offering a promising pathway for large-scale hydrogen production.
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.