{"title":"Enhanced Stability of Vanadium-Based Electrode Materials Using Multi-Component Hybrids for High-Performance Zinc-Ion Batteries","authors":"Zhiqiang Dai, Xueqing Zhang, Kittima Lolupiman, Chengwu Yang, Pattaraporn Woottapanit, Wanwisa Limphirat, Suttipong Wannapaiboon, Xinyu Zhang, Jiaqian Qin","doi":"10.1021/acsami.5c13283","DOIUrl":null,"url":null,"abstract":"The limited availability of cathode materials for rechargeable aqueous zinc-ion batteries (ZIBs), which have great potential for grid-scale energy storage applications, remains a significant obstacle to development. In this study, we proposed a Li<sub>3</sub>VO<sub>4</sub>–LiV<sub>2</sub>O<sub>5</sub>-based (LiVO-w) nanocomposite structure obtained by simple high-temperature calcination and water washing as a high-performance cathode. The LiVO-w cathode demonstrates a high specific capacity (310.43 mAh g<sup>–1</sup> at 1 A g<sup>–1</sup> and 130.52 mAh g<sup>–1</sup> at 20 A g<sup>–1</sup>) and excellent cycling stability (100% capacity retention after 4000 cycles at 10 A g<sup>–1</sup> and 85.13% capacity retention after 10,000 cycles). In addition, ex situ X-ray diffraction (XRD) shows the structural transformation of LiVO-w during the self-assembly process. During the first charge process, the multivalent and multistructured LiVO-w undergoes an increase in the valence of V, accompanied by the generation of Zn<sub>3</sub>(OH)<sub>2</sub>V<sub>2</sub>O<sub>7</sub>·H<sub>2</sub>O on the surface of the matrix. The charge and discharge process after self-assembly mainly corresponds to the generation and decomposition of Zn<sub>3</sub>(OH)<sub>2</sub>V<sub>2</sub>O<sub>7</sub>·H<sub>2</sub>O. This excellent self-assembled matrix realizes the realization of LiVO-w cathodes with high capacity and high-capacity retention, representing a major advancement in the commercial development of ZIBs for the development of LiVO-w positive electrode materials.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"7 1","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.5c13283","RegionNum":2,"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
Abstract
The limited availability of cathode materials for rechargeable aqueous zinc-ion batteries (ZIBs), which have great potential for grid-scale energy storage applications, remains a significant obstacle to development. In this study, we proposed a Li3VO4–LiV2O5-based (LiVO-w) nanocomposite structure obtained by simple high-temperature calcination and water washing as a high-performance cathode. The LiVO-w cathode demonstrates a high specific capacity (310.43 mAh g–1 at 1 A g–1 and 130.52 mAh g–1 at 20 A g–1) and excellent cycling stability (100% capacity retention after 4000 cycles at 10 A g–1 and 85.13% capacity retention after 10,000 cycles). In addition, ex situ X-ray diffraction (XRD) shows the structural transformation of LiVO-w during the self-assembly process. During the first charge process, the multivalent and multistructured LiVO-w undergoes an increase in the valence of V, accompanied by the generation of Zn3(OH)2V2O7·H2O on the surface of the matrix. The charge and discharge process after self-assembly mainly corresponds to the generation and decomposition of Zn3(OH)2V2O7·H2O. This excellent self-assembled matrix realizes the realization of LiVO-w cathodes with high capacity and high-capacity retention, representing a major advancement in the commercial development of ZIBs for the development of LiVO-w positive electrode materials.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.