材料科学
阴极
降级(电信)
离子
化学物理
晶间腐蚀
阳极
相(物质)
化学工程
复合材料
微观结构
化学
电极
电信
工程类
物理化学
有机化学
计算机科学
作者
Chao Xu,Katharina Märker,Juhan Lee,Amoghavarsha Mahadevegowda,Philip J. Reeves,Sarah J. Day,Matthias F. Groh,Steffen Emge,Caterina Ducati,B. Layla Mehdi,Chiu C. Tang,Clare P. Grey
出处
期刊:Nature Materials
[Springer Nature]
日期:2020-08-24
卷期号:20 (1): 84-92
被引量:447
标识
DOI:10.1038/s41563-020-0767-8
摘要
Ni-rich layered cathode materials are among the most promising candidates for high-energy-density Li-ion batteries, yet their degradation mechanisms are still poorly understood. We report a structure-driven degradation mechanism for NMC811 (LiNi0.8Mn0.1Co0.1O2), in which a proportion of the material exhibits a lowered accessible state of charge at the end of charging after repetitive cycling and becomes fatigued. Operando synchrotron long-duration X-ray diffraction enabled by a laser-thinned coin cell shows the emergence and growth in the concentration of this fatigued phase with cycle number. This degradation is structure driven and is not solely due to kinetic limitations or intergranular cracking: no bulk phase transformations, no increase in Li/Ni antisite mixing and no notable changes in the local structure or Li-ion mobility of the bulk are seen in aged NMCs. Instead, we propose that this degradation stems from the high interfacial lattice strain between the reconstructed surface and the bulk layered structure that develops when the latter is at states of charge above a distinct threshold of approximately 75%. This mechanism is expected to be universal in Ni-rich layered cathodes. Our findings provide fundamental insights into strategies to help mitigate this degradation process.
科研通智能强力驱动
Strongly Powered by AbleSci AI