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Onset Potential for Electrolyte Oxidation and Ni-Rich Cathode Degradation in Lithium-Ion Batteries

[Image: see text] High-capacity Ni-rich layered metal oxide cathodes are highly desirable to increase the energy density of lithium-ion batteries. However, these materials suffer from poor cycling performance, which is exacerbated by increased cell voltage. We demonstrate here the detrimental effect...

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Detalles Bibliográficos
Autores principales: Dose, Wesley M., Li, Weiqun, Temprano, Israel, O’Keefe, Christopher A., Mehdi, B. Layla, De Volder, Michael F. L., Grey, Clare P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578037/
https://www.ncbi.nlm.nih.gov/pubmed/36277132
http://dx.doi.org/10.1021/acsenergylett.2c01722
Descripción
Sumario:[Image: see text] High-capacity Ni-rich layered metal oxide cathodes are highly desirable to increase the energy density of lithium-ion batteries. However, these materials suffer from poor cycling performance, which is exacerbated by increased cell voltage. We demonstrate here the detrimental effect of ethylene carbonate (EC), a core component in conventional electrolytes, when NMC811 (LiNi(0.8)Mn(0.1)Co(0.1)O(2)) is charged above 4.4 V vs Li/Li(+)—the onset potential for lattice oxygen release. Oxygen loss is enhanced by EC-containing electrolytes—compared to EC-free—and correlates with more electrolyte oxidation/breakdown and cathode surface degradation, which increase concurrently above 4.4 V. In contrast, NMC111 (LiNi(0.33)Mn(0.33)Co(0.33)O(2)), which does not release oxygen up to 4.6 V, shows a similar extent of degradation irrespective of the electrolyte. This work highlights the incompatibility between conventional EC-based electrolytes and Ni-rich cathodes (more generally, cathodes that release lattice oxygen such as Li-/Mn-rich and disordered rocksalt cathodes) and motivates further work on wider classes of electrolytes and additives.