瓶颈
锂(药物)
阴极
材料科学
电化学
储能
阳极
纳米技术
能量密度
相(物质)
氧化还原
比例(比率)
高能
锂离子电池
计算机科学
粒子(生态学)
离子
钥匙(锁)
电池(电)
电压
工作(物理)
电流密度
化学工程
容量损失
能量(信号处理)
机制(生物学)
工程物理
作者
Shu Zhang,Yong Lü,Zhenhua Yan,Jun Chen
出处
期刊:
[Elsevier BV]
日期:2026-10-01
卷期号:: 100157-100157
标识
DOI:10.1016/j.esen.2026.100157
摘要
Li-rich Mn-based oxides (LRM) have become key candidate materials for breaking through the energy density bottleneck of lithium-ion batteries due to their ultra-high specific capacity compared with that of traditional commercial cathodes. However, their practical applications have long been plagued by issues such as voltage fade and capacity decay, rooted in the intrinsic structural differences between Li 2 MnO 3 and LiNi x Co y Mn 1−x−y O 2 phases. This review systematically compares the structural and performance characteristics of mainstream inorganic cathodes, focusing on the electrochemical behavior and anion redox mechanism of LRM. It analyzes in depth the failure paths driven by two phase differences arising from mechanics, thermotics, electricity, and magnetism. Subsequently, multi-level structural modification strategies at the atomic, mesoscopic, and particle scale are summarized. Finally, the application and existing problems of LRM in solid-state batteries are discussed. This review aims to provide a systematic reference for the design optimization of LRM and their application in high-energy-density lithium batteries.
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