{"title":"Mg2+/Al3+ Co-doped Li-Rich Manganese-Based Oxides for Boosting Rate Performance and Stability of Lithium-Ion Batteries","authors":"Junxia Meng, Wenzhuan Hu, Quanxin Ma, Zhenzhen Wu, Lishuang Xu, Jie Huang, Chen Xiao, Junru Wang, Lina Zhang, Feng Liu, Xing Zhi, Shanqing Zhang","doi":"10.1002/adfm.202501762","DOIUrl":null,"url":null,"abstract":"Lithium-rich manganese-based oxides (LRMOs) are promising cathode materials for lithium-ion batteries (LIBs) due to their high energy density. However, their practical application is limited by poor rate performance and rapid capacity fading. Single elemental doping of LRMOs has only partly addressed these issues. In this study, a Mg<sup>2+</sup>/Al<sup>3+</sup> co-doping strategy is introduced to modify LRMO cathode materials. The theoretical and experimental investigations confirm that the proposed Mg<sup>2+</sup>/Al<sup>3+</sup> co-doping strategy can regulate the atomic configuration and spatial lattice structure, induce a coupling mechanism that promotes Li<sup>+</sup> diffusion kinetics, and enhance the overall lattice structural stability. As a result, the Mg<sup>2+</sup>/Al<sup>3+</sup> co-doped LRMO exhibits a high initial reversible capacity of 269.9 mAh g<sup>−1</sup>, superior rate capability with 160.7 mAh g<sup>−1</sup> at 5.0C, and excellent cycling stability with 90.0% capacity retention after 200 cycles at 1.0C. Furthermore, the co-doped LRMO pouch full cell delivers outstanding long-term cycling performance. The success of this work suggests that Mg<sup>2+</sup>/Al<sup>3+</sup> co-doping could be an excellent strategy to advance the LRMO cathode materials for high-capacity LIBs.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"10 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202501762","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Lithium-rich manganese-based oxides (LRMOs) are promising cathode materials for lithium-ion batteries (LIBs) due to their high energy density. However, their practical application is limited by poor rate performance and rapid capacity fading. Single elemental doping of LRMOs has only partly addressed these issues. In this study, a Mg2+/Al3+ co-doping strategy is introduced to modify LRMO cathode materials. The theoretical and experimental investigations confirm that the proposed Mg2+/Al3+ co-doping strategy can regulate the atomic configuration and spatial lattice structure, induce a coupling mechanism that promotes Li+ diffusion kinetics, and enhance the overall lattice structural stability. As a result, the Mg2+/Al3+ co-doped LRMO exhibits a high initial reversible capacity of 269.9 mAh g−1, superior rate capability with 160.7 mAh g−1 at 5.0C, and excellent cycling stability with 90.0% capacity retention after 200 cycles at 1.0C. Furthermore, the co-doped LRMO pouch full cell delivers outstanding long-term cycling performance. The success of this work suggests that Mg2+/Al3+ co-doping could be an excellent strategy to advance the LRMO cathode materials for high-capacity LIBs.
期刊介绍:
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