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

被引:80
作者
Dose, Wesley M. [1 ,2 ,3 ]
Li, Weiqun [2 ]
Temprano, Israel [3 ]
O'Keefe, Christopher A. [2 ,3 ]
Mehdi, B. Layla [2 ,4 ]
De Volder, Michael F. L. [1 ]
Grey, Clare P. [1 ,2 ]
机构
[1] Univ Cambridge, Dept Engn, Cambridge CB3 0FS, Cambridgeshire, England
[2] Faraday Inst, Didcot OX11 0RA, Oxfordshire, England
[3] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, Cambridgeshire, England
[4] Univ Liverpool, Dept Mech, Mat & Aerosp Engn, Liverpool L69 3GH, Lancashire, England
基金
英国工程与自然科学研究理事会;
关键词
LAYERED OXIDE CATHODES; TRANSITION-METAL IONS; DECOMPOSITION REACTIONS; DISSOLUTION; STABILITY; SURFACE; NMC; REDUCTION; EVOLUTION; MIGRATION;
D O I
10.1021/acsenergylett.2c01722
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 (LiNi0.8Mn0.1Co0.1O2) 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 (LiNi0.33Mn0.33Co0.33O2), 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.
引用
收藏
页码:3524 / 3530
页数:7
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