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Onset Potential for Electrolyte Oxidation and Ni-Rich Cathode Degradation in Lithium-Ion Batteries
Author(s) -
Wesley M. Dose,
Weiqun Li,
Israel Temprano,
Christopher A. O’Keefe,
B. Layla Mehdi,
Michael F. L. De Volder,
Clare P. Grey
Publication year - 2022
Publication title -
acs energy letters
Language(s) - English
Resource type - Journals
ISSN - 2380-8195
DOI - 10.1021/acsenergylett.2c01722
Subject(s) - electrolyte , cathode , oxide , oxygen , materials science , chemical engineering , lithium (medication) , inorganic chemistry , degradation (telecommunications) , electrode , chemistry , metallurgy , electrical engineering , medicine , organic chemistry , engineering , endocrinology
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.

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