{"title":"掺杂碳纳米管负载NiMoO4/Ni异质结构作为高效碱水/海水析氢反应的电催化剂","authors":"Wenting Zhang, , , Yuzheng Chen, , , Ruobing Li, , and , Sijia Li*, ","doi":"10.1021/acs.energyfuels.5c02928","DOIUrl":null,"url":null,"abstract":"<p >Electrocatalytic water splitting is a promising green technology for hydrogen production, but its industrial application faces two major challenges: slow kinetics of the hydrogen evolution reaction (HER) and insufficient catalyst durability. These limitations are particularly evident in corrosive seawater environments, where accelerated catalyst deactivation severely hampers practical applications. In this paper, a B-doped carbon nanotube-supported NiMoO<sub>4</sub>/Ni heterostructure catalyst (NiMoO<sub>4</sub>/Ni/B-CNTs) is synthesized via a hydrothermal-calcination method. The NiMoO<sub>4</sub>/Ni/B-CNTs catalyst exhibits outstanding HER activity, showing overpotentials of 42 mV (1 M KOH) and 48 mV (alkaline seawater) at 10 mA cm<sup>–2</sup>, respectively, comparable to that of noble metal Pt/C, indicating notable superiority in the HER field. Remarkably, the NiMoO<sub>4</sub>/Ni/B-CNTs remain stable after 10,000 cycles of cyclic voltammetry (CV) and 200 h of continuous operation in alkaline freshwater and alkaline seawater environments, with 95% current density retention, demonstrating their potential for hydrogen production on an industrial scale. The superior HER performance of NiMoO<sub>4</sub>/Ni/B-CNTs is attributed to the interfacial effect between NiMoO<sub>4</sub> and Ni, and the synergistic effect between the B-CNTs supports and NiMoO<sub>4</sub>/Ni, which collectively facilitates the HER process. This study opens a potential path for the development of nonprecious metal efficient HER electrocatalysts for alkaline freshwater/seawater electrolysis.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 40","pages":"19388–19399"},"PeriodicalIF":5.3000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"NiMoO4/Ni Heterostructure Supported on B-Doped Carbon Nanotubes as a Robust Electrocatalyst for Efficient Alkaline Water/Seawater Hydrogen Evolution Reaction\",\"authors\":\"Wenting Zhang, , , Yuzheng Chen, , , Ruobing Li, , and , Sijia Li*, \",\"doi\":\"10.1021/acs.energyfuels.5c02928\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Electrocatalytic water splitting is a promising green technology for hydrogen production, but its industrial application faces two major challenges: slow kinetics of the hydrogen evolution reaction (HER) and insufficient catalyst durability. These limitations are particularly evident in corrosive seawater environments, where accelerated catalyst deactivation severely hampers practical applications. In this paper, a B-doped carbon nanotube-supported NiMoO<sub>4</sub>/Ni heterostructure catalyst (NiMoO<sub>4</sub>/Ni/B-CNTs) is synthesized via a hydrothermal-calcination method. The NiMoO<sub>4</sub>/Ni/B-CNTs catalyst exhibits outstanding HER activity, showing overpotentials of 42 mV (1 M KOH) and 48 mV (alkaline seawater) at 10 mA cm<sup>–2</sup>, respectively, comparable to that of noble metal Pt/C, indicating notable superiority in the HER field. Remarkably, the NiMoO<sub>4</sub>/Ni/B-CNTs remain stable after 10,000 cycles of cyclic voltammetry (CV) and 200 h of continuous operation in alkaline freshwater and alkaline seawater environments, with 95% current density retention, demonstrating their potential for hydrogen production on an industrial scale. The superior HER performance of NiMoO<sub>4</sub>/Ni/B-CNTs is attributed to the interfacial effect between NiMoO<sub>4</sub> and Ni, and the synergistic effect between the B-CNTs supports and NiMoO<sub>4</sub>/Ni, which collectively facilitates the HER process. This study opens a potential path for the development of nonprecious metal efficient HER electrocatalysts for alkaline freshwater/seawater electrolysis.</p>\",\"PeriodicalId\":35,\"journal\":{\"name\":\"Energy & Fuels\",\"volume\":\"39 40\",\"pages\":\"19388–19399\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2025-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Fuels\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c02928\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c02928","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
摘要
电催化水裂解是一种很有前途的绿色制氢技术,但其工业应用面临着析氢反应动力学缓慢和催化剂耐久性不足两大挑战。这些限制在腐蚀性海水环境中尤为明显,在这种环境中,催化剂的加速失活严重阻碍了实际应用。本文采用水热煅烧的方法合成了一种b掺杂碳纳米管负载的NiMoO4/Ni异质结构催化剂(NiMoO4/Ni/B-CNTs)。NiMoO4/Ni/B-CNTs催化剂表现出优异的HER活性,在10 mA cm-2下的过电位分别为42 mV (1 M KOH)和48 mV(碱性海水),与贵金属Pt/C相当,在HER领域具有明显的优势。值得注意的是,NiMoO4/Ni/B-CNTs在碱性淡水和碱性海水环境中经过1万次循环伏安(CV)和200小时的连续运行后仍保持稳定,电流密度保持95%,证明了其在工业规模上制氢的潜力。NiMoO4/Ni/B-CNTs优异的HER性能归因于NiMoO4与Ni之间的界面效应,以及B-CNTs载体与NiMoO4/Ni之间的协同效应,共同促进了HER过程的进行。本研究为开发非贵金属高效的碱性淡水/海水电解HER电催化剂开辟了一条潜在的途径。
NiMoO4/Ni Heterostructure Supported on B-Doped Carbon Nanotubes as a Robust Electrocatalyst for Efficient Alkaline Water/Seawater Hydrogen Evolution Reaction
Electrocatalytic water splitting is a promising green technology for hydrogen production, but its industrial application faces two major challenges: slow kinetics of the hydrogen evolution reaction (HER) and insufficient catalyst durability. These limitations are particularly evident in corrosive seawater environments, where accelerated catalyst deactivation severely hampers practical applications. In this paper, a B-doped carbon nanotube-supported NiMoO4/Ni heterostructure catalyst (NiMoO4/Ni/B-CNTs) is synthesized via a hydrothermal-calcination method. The NiMoO4/Ni/B-CNTs catalyst exhibits outstanding HER activity, showing overpotentials of 42 mV (1 M KOH) and 48 mV (alkaline seawater) at 10 mA cm–2, respectively, comparable to that of noble metal Pt/C, indicating notable superiority in the HER field. Remarkably, the NiMoO4/Ni/B-CNTs remain stable after 10,000 cycles of cyclic voltammetry (CV) and 200 h of continuous operation in alkaline freshwater and alkaline seawater environments, with 95% current density retention, demonstrating their potential for hydrogen production on an industrial scale. The superior HER performance of NiMoO4/Ni/B-CNTs is attributed to the interfacial effect between NiMoO4 and Ni, and the synergistic effect between the B-CNTs supports and NiMoO4/Ni, which collectively facilitates the HER process. This study opens a potential path for the development of nonprecious metal efficient HER electrocatalysts for alkaline freshwater/seawater electrolysis.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.