材料科学
氧化还原
电化学
电子结构
原位
阴极
离子
格子(音乐)
纳米技术
化学物理
化学计量学
联轴节(管道)
合理设计
电极
工作(物理)
化学工程
数码产品
结构稳定性
电化学储能
调制(音乐)
普鲁士蓝
材料设计
蓝图
不稳定性
设计要素和原则
晶体结构
作者
Wontae Lee,Yun Seong Byeon,Kyeongkeun Kwon,Jae‐Uk Kim,Seongeun Lee,Dong Ki Kim,Bo Gyu Jang,Min Park,Won‐Sub Yoon
标识
DOI:10.1002/adma.202518963
摘要
ABSTRACT Disordered cathode materials are attractive candidates for next‐generation lithium‐ion batteries (LIBs), but the intrinsic instability of anionic redox hinders their commercialization. Unlike conventional Li‐excess disordered systems limited by compositional constraints of Li 1+x M 1‐x O 2 , Immm ‐Li 2 NiO 2 offers a platform to access highly lithiated chemistries that enable in situ disorder formation during electrochemical cycling. This allows lattice O to contribute to charge compensation; however, O 2 release at high voltages compromises reversibility and cycling stability. To address this, fluorination generates a quadrupolar Li‐O‐M‐F configuration that lowers the Li─O─Li band energy level and delays the onset of anionic redox. This electronic structure modification suppresses O 2 evolution, enhances structural stability, and improves cycling performance. By coupling electrochemically induced disorder with stabilization through Li‐O‐M‐F units, this work establishes a new framework for engineering durable, high‐capacity cathodes, offering a blueprint for material design strategies that transcend stoichiometric restrictions and unlock stable anion redox functionality.
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