{"title":"Phase control of MoWS2 nanostructures via oxalic acid-assisted electron injection: From molybdenum disulfide to tungsten disulfide","authors":"Xiao-Yu Chen, Yuan Zhao, Zi-Han Liu, Yi-Tong Pang, Di-Gen Wei, Jing-Yi Wangchen, Cheng-Bao Yao","doi":"10.1016/j.cej.2025.162031","DOIUrl":null,"url":null,"abstract":"Metallic-phase molybdenum disulfide (1T-MoS<sub>2</sub>) and tungsten disulfide (1T-WS<sub>2</sub>) have attracted great attention due to their excellent performance in the field of electrochemical hydrogen evolution catalysis. Recent studies have demonstrated that reducing the potential barrier of lattice distortion and injecting electrons into materials are the keys to synthesizing 1T phase transition metal dichalcogenides (1T-TMDs) materials with long-term stability. Here, a novel synthesis strategy for 1T-TMDs was proposed. With the assistance of oxalic acid, the continuous synthesis from semiconductor-phase (2H) MoS<sub>2</sub> to 1T-MoWS<sub>2</sub> and then to 2H-WS<sub>2</sub> was achieved by changing the proportion of precursors. The 1T-phase of MoWS<sub>2</sub> has a proportion of 74.36 %. Phase transformation mechanism analysis shows that the construction of the ternary structure reduces the lattice distortion barrier, and oxalic acid directly injects electrons into the ternary structure, providing a driving force for the formation and stabilization of the 1T-phase. Compared with the 2H-phase, the 1T-phase MoWS<sub>2</sub> has significantly optimized electrochemical catalytic performance. Density functional calculations and transient absorption results revealed that the origin of the efficient catalytic performance of 1T-phase MoWS<sub>2</sub>, with special electronic structure being the main reason. This study provides a new strategy for the structural design and synthesis of high-efficiency 1T phase catalysts","PeriodicalId":270,"journal":{"name":"Chemical Engineering Journal","volume":"292 1","pages":""},"PeriodicalIF":13.3000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.cej.2025.162031","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Metallic-phase molybdenum disulfide (1T-MoS2) and tungsten disulfide (1T-WS2) have attracted great attention due to their excellent performance in the field of electrochemical hydrogen evolution catalysis. Recent studies have demonstrated that reducing the potential barrier of lattice distortion and injecting electrons into materials are the keys to synthesizing 1T phase transition metal dichalcogenides (1T-TMDs) materials with long-term stability. Here, a novel synthesis strategy for 1T-TMDs was proposed. With the assistance of oxalic acid, the continuous synthesis from semiconductor-phase (2H) MoS2 to 1T-MoWS2 and then to 2H-WS2 was achieved by changing the proportion of precursors. The 1T-phase of MoWS2 has a proportion of 74.36 %. Phase transformation mechanism analysis shows that the construction of the ternary structure reduces the lattice distortion barrier, and oxalic acid directly injects electrons into the ternary structure, providing a driving force for the formation and stabilization of the 1T-phase. Compared with the 2H-phase, the 1T-phase MoWS2 has significantly optimized electrochemical catalytic performance. Density functional calculations and transient absorption results revealed that the origin of the efficient catalytic performance of 1T-phase MoWS2, with special electronic structure being the main reason. This study provides a new strategy for the structural design and synthesis of high-efficiency 1T phase catalysts
期刊介绍:
The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.