Jinhua Zhou, Tao Ji, Shengyang Xu, Xiong Wang, Juntao Wang, Yating Tang, Yuhong Li, Wenyu Yin, Hongmei Ji, Shaojun Shi, Gang Yang
{"title":"协同设计具有界面共价键的高倍率钠离子电池用无碳MoS2/MoO2异质结构阳极。","authors":"Jinhua Zhou, Tao Ji, Shengyang Xu, Xiong Wang, Juntao Wang, Yating Tang, Yuhong Li, Wenyu Yin, Hongmei Ji, Shaojun Shi, Gang Yang","doi":"10.1002/chem.202500589","DOIUrl":null,"url":null,"abstract":"<p>The development of hierarchical heterostructured materials for sodium-ion batteries (SIBs) remains hindered by suboptimal high-rate cycling performance, primarily due to phase interface pulverization and separation during charge–discharge processes. To address these challenges, we designed a carbon-free hierarchical structure comprising few-layered MoS₂ nanosheets and MoO₂ nanocrystals through precise compositional optimization and rational structural engineering. The heterogeneous components are interconnected through robust S─O covalent bonds, which theoretical calculations and experimental results confirm generate a built-in electric field at the heterointerfaces, significantly enhancing reaction kinetics. Crucially, these covalent bonds stabilize the heterointerfaces, improving structural integrity and mitigating electrode material agglomeration and pulverization. Additionally, the MoS₂/MoO₂ heterostructure enhances Na⁺ adsorption energetics and reduces Na⁺ diffusion barriers, facilitating efficient ion transport. Leveraging its abundant heterointerfaces and stable architecture, the composite delivers exceptional rate performance (432.7 mAh·g⁻¹ at 10 A·g⁻¹) and outstanding cycling stability (nearly 100% capacity retention over 400 cycles at 5 A·g⁻¹). This work provides a strategic framework for designing heterostructured materials with stable interface-rich architectures, advancing the development of high-performance conversion/alloy-type anodes for energy storage applications.</p>","PeriodicalId":144,"journal":{"name":"Chemistry - A European Journal","volume":"31 27","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistically Designed Carbon-Free MoS2/MoO2 Heterostructure Anodes with Interfacial Covalent Bonds for High-Rate Sodium-Ion Batteries\",\"authors\":\"Jinhua Zhou, Tao Ji, Shengyang Xu, Xiong Wang, Juntao Wang, Yating Tang, Yuhong Li, Wenyu Yin, Hongmei Ji, Shaojun Shi, Gang Yang\",\"doi\":\"10.1002/chem.202500589\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The development of hierarchical heterostructured materials for sodium-ion batteries (SIBs) remains hindered by suboptimal high-rate cycling performance, primarily due to phase interface pulverization and separation during charge–discharge processes. To address these challenges, we designed a carbon-free hierarchical structure comprising few-layered MoS₂ nanosheets and MoO₂ nanocrystals through precise compositional optimization and rational structural engineering. The heterogeneous components are interconnected through robust S─O covalent bonds, which theoretical calculations and experimental results confirm generate a built-in electric field at the heterointerfaces, significantly enhancing reaction kinetics. Crucially, these covalent bonds stabilize the heterointerfaces, improving structural integrity and mitigating electrode material agglomeration and pulverization. Additionally, the MoS₂/MoO₂ heterostructure enhances Na⁺ adsorption energetics and reduces Na⁺ diffusion barriers, facilitating efficient ion transport. Leveraging its abundant heterointerfaces and stable architecture, the composite delivers exceptional rate performance (432.7 mAh·g⁻¹ at 10 A·g⁻¹) and outstanding cycling stability (nearly 100% capacity retention over 400 cycles at 5 A·g⁻¹). This work provides a strategic framework for designing heterostructured materials with stable interface-rich architectures, advancing the development of high-performance conversion/alloy-type anodes for energy storage applications.</p>\",\"PeriodicalId\":144,\"journal\":{\"name\":\"Chemistry - A European Journal\",\"volume\":\"31 27\",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-03-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry - A European Journal\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202500589\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - A European Journal","FirstCategoryId":"92","ListUrlMain":"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202500589","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Synergistically Designed Carbon-Free MoS2/MoO2 Heterostructure Anodes with Interfacial Covalent Bonds for High-Rate Sodium-Ion Batteries
The development of hierarchical heterostructured materials for sodium-ion batteries (SIBs) remains hindered by suboptimal high-rate cycling performance, primarily due to phase interface pulverization and separation during charge–discharge processes. To address these challenges, we designed a carbon-free hierarchical structure comprising few-layered MoS₂ nanosheets and MoO₂ nanocrystals through precise compositional optimization and rational structural engineering. The heterogeneous components are interconnected through robust S─O covalent bonds, which theoretical calculations and experimental results confirm generate a built-in electric field at the heterointerfaces, significantly enhancing reaction kinetics. Crucially, these covalent bonds stabilize the heterointerfaces, improving structural integrity and mitigating electrode material agglomeration and pulverization. Additionally, the MoS₂/MoO₂ heterostructure enhances Na⁺ adsorption energetics and reduces Na⁺ diffusion barriers, facilitating efficient ion transport. Leveraging its abundant heterointerfaces and stable architecture, the composite delivers exceptional rate performance (432.7 mAh·g⁻¹ at 10 A·g⁻¹) and outstanding cycling stability (nearly 100% capacity retention over 400 cycles at 5 A·g⁻¹). This work provides a strategic framework for designing heterostructured materials with stable interface-rich architectures, advancing the development of high-performance conversion/alloy-type anodes for energy storage applications.
期刊介绍:
Chemistry—A European Journal is a truly international journal with top quality contributions (2018 ISI Impact Factor: 5.16). It publishes a wide range of outstanding Reviews, Minireviews, Concepts, Full Papers, and Communications from all areas of chemistry and related fields.
Based in Europe Chemistry—A European Journal provides an excellent platform for increasing the visibility of European chemistry as well as for featuring the best research from authors from around the world.
All manuscripts are peer-reviewed, and electronic processing ensures accurate reproduction of text and data, plus short publication times.
The Concepts section provides nonspecialist readers with a useful conceptual guide to unfamiliar areas and experts with new angles on familiar problems.
Chemistry—A European Journal is published on behalf of ChemPubSoc Europe, a group of 16 national chemical societies from within Europe, and supported by the Asian Chemical Editorial Societies. The ChemPubSoc Europe family comprises: Angewandte Chemie, Chemistry—A European Journal, European Journal of Organic Chemistry, European Journal of Inorganic Chemistry, ChemPhysChem, ChemBioChem, ChemMedChem, ChemCatChem, ChemSusChem, ChemPlusChem, ChemElectroChem, and ChemistryOpen.