| Literature DB >> 32839589 |
Chao Xu1,2, Katharina Märker1,2, Juhan Lee2,3, Amoghavarsha Mahadevegowda2,4, Philip J Reeves1,2, Sarah J Day5, Matthias F Groh1,6, Steffen P Emge1, Caterina Ducati2,4, B Layla Mehdi2,3, Chiu C Tang5, Clare P Grey7,8.
Abstract
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.Entities:
Year: 2020 PMID: 32839589 DOI: 10.1038/s41563-020-0767-8
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841