碳酸乙烯酯
材料科学
电解质
降级(电信)
锂(药物)
碳酸盐
离子
乙烯
无机化学
碳酸锂
化学工程
电极
冶金
有机化学
催化作用
化学
离子键合
物理化学
内分泌学
工程类
电信
医学
计算机科学
作者
Jason S. Terreblanche,Tongjun Luo,Louis F. J. Piper,Wesley M. Dose
标识
DOI:10.1002/aenm.202404427
摘要
Abstract The development of stable electrolyte solutions is critical for improving the lifetime and performance of lithium‐ion batteries (LIBs). Electrolyte instability is a prominent issue with many next‐generation electrode materials, such as Ni‐rich cathodes, with recent reports identifying ethylene carbonate (EC) as a bad actor at the cathode surface. Herein, electrochemical methods, operando pressure measurements, and post‐mortem X‐ray and solution NMR studies are combined to investigate electrolyte and interfacial degradation phenomena in Ni‐rich LiNi 0.8 Mn 0.1 Co 0.1 O 2 (NMC811)/graphite full cells with EC‐containing and EC‐free electrolytes. One key finding is that the mechanism for improved performance in EC‐free electrolyte–1.5 M LiPF 6 in ethyl methyl carbonate (EMC) with 10 wt.% fluoroethylene carbonate (FEC)–arises from improved stability at both electrode‐electrolyte interfaces. The EC‐free electrolyte is found to suppress lattice oxygen release and reduce surface layer formation at NMC, leading to improved ion transport into the cathode particles, suppressed electrolyte solvent oxidation reactions, less formation and crossover of species that disrupt the graphite solid electrolyte interphase (SEI), and ultimately improved capacity retention. These insights are helpful in understanding and mitigating degradation in LIBs with Ni‐rich cathodes.
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