Xiaoyang Zhao, Jian Wang, Yunfei Zhang, Ying Dong, Yuqin Yin, Zhanghu Yu, Guanren Ge, Jun Yu, Shichun Mu
{"title":"CoS2 Hybridized Mo-Doped VS4 Core-Shell Three-Dimensional Nanoarrays for Efficient Hydrogen Evolution Reaction","authors":"Xiaoyang Zhao, Jian Wang, Yunfei Zhang, Ying Dong, Yuqin Yin, Zhanghu Yu, Guanren Ge, Jun Yu, Shichun Mu","doi":"10.1016/j.jallcom.2025.179346","DOIUrl":null,"url":null,"abstract":"Non-precious metal electrocatalysts can effectively reduce the hydrogen production industry's dependence on precious metal catalysts. This study reports a non-precious metal cobalt sulfide hybrid molybdenum-doped vanadium tetrasulfide (CoS<sub>2</sub>@Mo-VS<sub>4</sub>) core-shell nanorod catalyst for hydrogen evolution reactions, which demonstrates excellent catalytic performance in acidic electrolytes. The core-shell structured nanoarray, consisting of cobalt sulfide core and molybdenum-doped vanadium tetrasulfide shell, is fabricated on carbon cloth via a hydrothermal method. This design effectively prevents aggregation, and the significant spatial arrangement in the nanoarrays facilitates electrolyte ion transport and bubble release. The core-shell heterointerface provides a fast channel for electron transfer, reducing electron transport resistance. Strong interactions between different components in the core-shell structure enable the tuning of electronic structure, enhancing catalytic performance. Results show that CoS<sub>2</sub>@Mo-VS<sub>4</sub>@CC exhibits superior hydrogen evolution performance in 0.5<!-- --> <!-- -->M H<sub>2</sub>SO<sub>4</sub>, requiring only 73<!-- --> <!-- -->mV (114<!-- --> <!-- -->mV) overpotential at current densities of 10<!-- --> <!-- -->mA∙cm⁻<sup>2</sup> (50<!-- --> <!-- -->mA∙cm⁻<sup>2</sup>). This provides a feasible strategy for designing efficient vanadium tetrasulfide electrocatalysts.KeywordsVS<sub>4</sub>, CoS<sub>2</sub>, core-shell structure, molybdenum doping, hydrogen evolution reaction","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"66 1","pages":""},"PeriodicalIF":6.3000,"publicationDate":"2025-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alloys and Compounds","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.jallcom.2025.179346","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Non-precious metal electrocatalysts can effectively reduce the hydrogen production industry's dependence on precious metal catalysts. This study reports a non-precious metal cobalt sulfide hybrid molybdenum-doped vanadium tetrasulfide (CoS2@Mo-VS4) core-shell nanorod catalyst for hydrogen evolution reactions, which demonstrates excellent catalytic performance in acidic electrolytes. The core-shell structured nanoarray, consisting of cobalt sulfide core and molybdenum-doped vanadium tetrasulfide shell, is fabricated on carbon cloth via a hydrothermal method. This design effectively prevents aggregation, and the significant spatial arrangement in the nanoarrays facilitates electrolyte ion transport and bubble release. The core-shell heterointerface provides a fast channel for electron transfer, reducing electron transport resistance. Strong interactions between different components in the core-shell structure enable the tuning of electronic structure, enhancing catalytic performance. Results show that CoS2@Mo-VS4@CC exhibits superior hydrogen evolution performance in 0.5 M H2SO4, requiring only 73 mV (114 mV) overpotential at current densities of 10 mA∙cm⁻2 (50 mA∙cm⁻2). This provides a feasible strategy for designing efficient vanadium tetrasulfide electrocatalysts.KeywordsVS4, CoS2, core-shell structure, molybdenum doping, hydrogen evolution reaction
期刊介绍:
The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.