{"title":"Corrosion-resistant single-atom catalysts for direct seawater electrolysis.","authors":"Yue Zhang, Weikang Wan, Yudi Peng, Yujun Guo, Jialing Zhou, Shengchen Wang, Jiayao Yuan, Yuru Liao, Linsheng Liu, Yifan Zhang, Suli Liu, Dingsheng Wang, Zhihui Dai","doi":"10.1093/nsr/nwaf060","DOIUrl":null,"url":null,"abstract":"<p><p>Direct seawater electrolysis (DSE) for hydrogen production is an appealing method for renewable energy storage. However, DSE faces challenges such as slow reaction kinetics, impurities, the competing chlorine evolution reaction at the anode, and membrane fouling, making it more complex than freshwater electrolysis. Therefore, developing catalysts with excellent stability under corrosion and fulfilling activity is vital to the advancement of DSE. Single-atom catalysts (SACs) with excellent tunability, high selectivity and high active sites demonstrate considerable potential for use in the electrolysis of seawater. In this review, we present the anodic and cathodic reaction mechanisms that occur during seawater cracking. Subsequently, to meet the challenges of DSE, rational strategies for modulating SACs are explored, including axial ligand engineering, carrier effects and protective layer coverage. Then, the application of <i>in-situ</i> characterization techniques and theoretical calculations to SACs is discussed with the aim of elucidating the intrinsic factors responsible for their efficient electrocatalysis. Finally, the process of scaling up monoatomic catalysts for the electrolysis of seawater is described, and some prospective insights are provided.</p>","PeriodicalId":18842,"journal":{"name":"National Science Review","volume":"12 4","pages":"nwaf060"},"PeriodicalIF":16.3000,"publicationDate":"2025-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11960101/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"National Science Review","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1093/nsr/nwaf060","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Direct seawater electrolysis (DSE) for hydrogen production is an appealing method for renewable energy storage. However, DSE faces challenges such as slow reaction kinetics, impurities, the competing chlorine evolution reaction at the anode, and membrane fouling, making it more complex than freshwater electrolysis. Therefore, developing catalysts with excellent stability under corrosion and fulfilling activity is vital to the advancement of DSE. Single-atom catalysts (SACs) with excellent tunability, high selectivity and high active sites demonstrate considerable potential for use in the electrolysis of seawater. In this review, we present the anodic and cathodic reaction mechanisms that occur during seawater cracking. Subsequently, to meet the challenges of DSE, rational strategies for modulating SACs are explored, including axial ligand engineering, carrier effects and protective layer coverage. Then, the application of in-situ characterization techniques and theoretical calculations to SACs is discussed with the aim of elucidating the intrinsic factors responsible for their efficient electrocatalysis. Finally, the process of scaling up monoatomic catalysts for the electrolysis of seawater is described, and some prospective insights are provided.
期刊介绍:
National Science Review (NSR; ISSN abbreviation: Natl. Sci. Rev.) is an English-language peer-reviewed multidisciplinary open-access scientific journal published by Oxford University Press under the auspices of the Chinese Academy of Sciences.According to Journal Citation Reports, its 2021 impact factor was 23.178.
National Science Review publishes both review articles and perspectives as well as original research in the form of brief communications and research articles.