{"title":"一步法构建协同效应高效双功能绿色制氢催化剂","authors":"Wansen Ma, Jinshuai Fei, Chao Chen, Liwen Hu, Xuewei Lv, Jie Dang","doi":"10.1016/j.jmst.2024.12.054","DOIUrl":null,"url":null,"abstract":"The simplification of the process of electrolytic water catalyst preparation and the exploitation of highly active catalysts represent a meaningful but challenging task. Meanwhile, bifunctional electrolytic water catalysts are of great significance in improving electrolysis efficiency and simplifying catalyst preparation processes. In this study, we introduce Ru and V into CoTe, which exhibits intrinsic oxygenophilic properties, and couple it with hydrophilic and well-conducting MXene to overcome the sluggish alkaline kinetics of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The synthesized Ru,V co-doped CoTe@MXene (RVCTM) catalysts exhibited HER overpotentials of 34 and 116 mV and OER overpotentials of 249 and 320 mV at 10 and 100 mA cm<sup>−2</sup> current densities, respectively. Moreover, the catalysts demonstrated remarkable stability. Theoretical calculations demonstrated that the incorporation of Ru and V had a profound impact on the local electronic environments of Co and Te. In addition, the coupling with MXene resulted in charge redistribution at the heterogeneous interface. The combined effect of doping and heterostructure construction effectively optimizes the d-band center of the catalyst and reduces the adsorption energy barrier of reaction intermediates. This approach offers deep insights into the development of multifunctional catalysts.","PeriodicalId":16154,"journal":{"name":"Journal of Materials Science & Technology","volume":"5 1","pages":""},"PeriodicalIF":14.3000,"publicationDate":"2025-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"One-step approach for constructing synergistic effect-based high-performance bifunctional catalysts toward green hydrogen production\",\"authors\":\"Wansen Ma, Jinshuai Fei, Chao Chen, Liwen Hu, Xuewei Lv, Jie Dang\",\"doi\":\"10.1016/j.jmst.2024.12.054\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The simplification of the process of electrolytic water catalyst preparation and the exploitation of highly active catalysts represent a meaningful but challenging task. Meanwhile, bifunctional electrolytic water catalysts are of great significance in improving electrolysis efficiency and simplifying catalyst preparation processes. In this study, we introduce Ru and V into CoTe, which exhibits intrinsic oxygenophilic properties, and couple it with hydrophilic and well-conducting MXene to overcome the sluggish alkaline kinetics of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The synthesized Ru,V co-doped CoTe@MXene (RVCTM) catalysts exhibited HER overpotentials of 34 and 116 mV and OER overpotentials of 249 and 320 mV at 10 and 100 mA cm<sup>−2</sup> current densities, respectively. Moreover, the catalysts demonstrated remarkable stability. Theoretical calculations demonstrated that the incorporation of Ru and V had a profound impact on the local electronic environments of Co and Te. In addition, the coupling with MXene resulted in charge redistribution at the heterogeneous interface. The combined effect of doping and heterostructure construction effectively optimizes the d-band center of the catalyst and reduces the adsorption energy barrier of reaction intermediates. This approach offers deep insights into the development of multifunctional catalysts.\",\"PeriodicalId\":16154,\"journal\":{\"name\":\"Journal of Materials Science & Technology\",\"volume\":\"5 1\",\"pages\":\"\"},\"PeriodicalIF\":14.3000,\"publicationDate\":\"2025-02-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Science & Technology\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jmst.2024.12.054\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Science & Technology","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.jmst.2024.12.054","RegionNum":1,"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
摘要
简化电解水催化剂的制备工艺和开发高活性催化剂是一项有意义但具有挑战性的任务。同时,双功能电解水催化剂对于提高电解效率和简化催化剂制备工艺具有重要意义。在本研究中,我们将Ru和V引入具有固有亲氧特性的CoTe中,并将其与亲水性和导电性良好的MXene偶联,以克服析氢反应(HER)和析氧反应(OER)缓慢的碱性动力学。合成的Ru、V共掺杂CoTe@MXene (RVCTM)催化剂在10和100 mA cm−2电流密度下的HER过电位分别为34和116 mV, OER过电位分别为249和320 mV。此外,催化剂表现出显著的稳定性。理论计算表明,Ru和V的加入对Co和Te的局部电子环境产生了深远的影响。此外,与MXene的耦合导致在非均相界面处电荷重新分布。掺杂和异质结构构建的共同作用有效地优化了催化剂的d带中心,降低了反应中间体的吸附能垒。这种方法为多功能催化剂的发展提供了深刻的见解。
One-step approach for constructing synergistic effect-based high-performance bifunctional catalysts toward green hydrogen production
The simplification of the process of electrolytic water catalyst preparation and the exploitation of highly active catalysts represent a meaningful but challenging task. Meanwhile, bifunctional electrolytic water catalysts are of great significance in improving electrolysis efficiency and simplifying catalyst preparation processes. In this study, we introduce Ru and V into CoTe, which exhibits intrinsic oxygenophilic properties, and couple it with hydrophilic and well-conducting MXene to overcome the sluggish alkaline kinetics of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The synthesized Ru,V co-doped CoTe@MXene (RVCTM) catalysts exhibited HER overpotentials of 34 and 116 mV and OER overpotentials of 249 and 320 mV at 10 and 100 mA cm−2 current densities, respectively. Moreover, the catalysts demonstrated remarkable stability. Theoretical calculations demonstrated that the incorporation of Ru and V had a profound impact on the local electronic environments of Co and Te. In addition, the coupling with MXene resulted in charge redistribution at the heterogeneous interface. The combined effect of doping and heterostructure construction effectively optimizes the d-band center of the catalyst and reduces the adsorption energy barrier of reaction intermediates. This approach offers deep insights into the development of multifunctional catalysts.
期刊介绍:
Journal of Materials Science & Technology strives to promote global collaboration in the field of materials science and technology. It primarily publishes original research papers, invited review articles, letters, research notes, and summaries of scientific achievements. The journal covers a wide range of materials science and technology topics, including metallic materials, inorganic nonmetallic materials, and composite materials.