电解质
降级(电信)
锂(药物)
阴极
氧化物
氧气
材料科学
无机化学
化学工程
电极
化学
冶金
物理化学
电气工程
有机化学
内分泌学
工程类
医学
作者
Wesley M. Dose,Weiqun Li,Israel Temprano,Christopher A. O’Keefe,B. Layla Mehdi,Michael F. L. De Volder,Clare P. Grey
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-09-22
卷期号:7 (10): 3524-3530
被引量:127
标识
DOI:10.1021/acsenergylett.2c01722
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.
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