{"title":"Electrolyte-Induced Interfacial/Bulk Dual Regulation Enables Negligible Capacity Decay in Li-Rich Cathodes.","authors":"Tianqi Yang,Min Jiang,Jiatao Lou,Zhouyu Huang,Xingjun Li,Liuqi Wang,Qingru Zhou,Lun Li,Liuyi Hu,Wei Liu,Yuzhi He,Xingyu Wang,Zhengbo Liu,Wenkui Zhang,Jun Zhang,Xinhui Xia,Yang Ren,Qi Liu","doi":"10.1002/adma.72969","DOIUrl":null,"url":null,"abstract":"Lithium-rich manganese-based oxides (LRMO) suffer from rapid capacity decay, mainly driven by interfacial instability and bulk structural degradation associated with Jahn-Teller (J-T) distortion in Mn3+-rich regions. Such distortion accelerates surface oxygen activity, triggers nonuniform cathode electrolyte interphase (CEI) formation along with promoted parasitic reactions. Herein, we develop an electrolyte‑induced interfacial/bulk dual regulation strategy that enables negligible capacity decay in Li‑rich cathodes via coordinated interfacial/bulk regulation. In situ characterizations combined with interfacial compositional analyses confirm the dynamic formation of a thin, uniform, and robust LiF/LiBO2-rich CEI, which stabilizes surface oxygen species and suppresses interfacial side reactions. Meanwhile, local structural analyses combined with theoretical calculations reveal that fluorinated molecules regulate Mn into a low-spin configuration, thereby alleviating J-T distortion and preventing bulk structural degradation. Benefiting from this dual induced interfacial-bulk stabilization effect, LRMO||Li cells deliver an initial capacity of 219.6 mAh g-1 and retain 97.6% of their capacity after 400 cycles. This work provides a new pathway toward electrolyte-mediated dual stabilization and demonstrates the feasibility of mitigating capacity decay in Li-rich cathodes via electrolyte-induced interfacial/bulk regulation.","PeriodicalId":114,"journal":{"name":"Advanced Materials","volume":"17 1","pages":"e72969"},"PeriodicalIF":29.1000,"publicationDate":"2026-04-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adma.72969","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 (LRMO) suffer from rapid capacity decay, mainly driven by interfacial instability and bulk structural degradation associated with Jahn-Teller (J-T) distortion in Mn3+-rich regions. Such distortion accelerates surface oxygen activity, triggers nonuniform cathode electrolyte interphase (CEI) formation along with promoted parasitic reactions. Herein, we develop an electrolyte‑induced interfacial/bulk dual regulation strategy that enables negligible capacity decay in Li‑rich cathodes via coordinated interfacial/bulk regulation. In situ characterizations combined with interfacial compositional analyses confirm the dynamic formation of a thin, uniform, and robust LiF/LiBO2-rich CEI, which stabilizes surface oxygen species and suppresses interfacial side reactions. Meanwhile, local structural analyses combined with theoretical calculations reveal that fluorinated molecules regulate Mn into a low-spin configuration, thereby alleviating J-T distortion and preventing bulk structural degradation. Benefiting from this dual induced interfacial-bulk stabilization effect, LRMO||Li cells deliver an initial capacity of 219.6 mAh g-1 and retain 97.6% of their capacity after 400 cycles. This work provides a new pathway toward electrolyte-mediated dual stabilization and demonstrates the feasibility of mitigating capacity decay in Li-rich cathodes via electrolyte-induced interfacial/bulk regulation.
期刊介绍:
Advanced Materials, one of the world's most prestigious journals and the foundation of the Advanced portfolio, is the home of choice for best-in-class materials science for more than 30 years. Following this fast-growing and interdisciplinary field, we are considering and publishing the most important discoveries on any and all materials from materials scientists, chemists, physicists, engineers as well as health and life scientists and bringing you the latest results and trends in modern materials-related research every week.