材料科学
锂(药物)
固态
离子
阴极
纳米技术
磷酸钒锂电池
工程物理
固态化学
无机化学
电化学
物理化学
电极
有机化学
医学
化学
工程类
内分泌学
作者
Qing Huang,Jinquan Liu,Xinman Chen,Shouxin Zhang,Languang Lu,Dongsheng Ren,Minggao Ouyang,Xiang Liu
标识
DOI:10.1002/adma.202410006
摘要
Abstract Li‐rich Mn‐based (LRM) cathode materials, characterized by their high specific capacity (>250 mAh g − ¹) and cost‐effectiveness, represent promising candidates for next‐generation lithium‐ion batteries. However, their commercial application is hindered by rapid capacity degradation and voltage fading, which can be attributed to transition metal migration, lattice oxygen release, and the toxicity of Mn ions to the anode solid electrolyte interphase (SEI). Recently, the application of LRM cathode in all‐solid‐state batteries (ASSBs) has garnered significant interest, as this approach eliminates the liquid electrolyte, thereby suppressing transition metal crosstalk and solid–liquid interfacial side reactions. This review first examines the historical development, crystal structure, and mechanisms underlying the high capacity of LRM cathode materials. It then introduces the current challenges facing LRM cathode and the associated degradation mechanisms and proposes solutions to these issues. Additionally, it summarizes recent research on LRM materials in ASSBs and suggests strategies for improvement. Finally, the review discusses future research directions for LRM cathode materials, including optimized material design, bulk doping, surface coating, developing novel solid electrolytes, and interface engineering. This review aims to provide further insights and new perspectives on applying LRM cathode materials in ASSBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI