电解质
阴极
电化学
锂(药物)
溶解
钝化
高压
化学工程
化学
离子
离子键合
钴
相(物质)
材料科学
电极
无机化学
电压
纳米技术
有机化学
物理化学
电气工程
工程类
医学
图层(电子)
内分泌学
作者
Chaocang Weng,Meijia Qiu,Bingfang Wang,Jiaqi Yang,Wenjie Mai,Likun Pan,Sumei Huang,Jinliang Li
标识
DOI:10.1002/ange.202419539
摘要
Developing high‐voltage electrolytes to stabilize LiCoO2 (LCO) cycling remains a challenge in lithium‐ion batteries. Constructing a high‐quality cathode electrolyte interface (CEI) is essential to mitigate adverse reactions at high voltages. However, conventional inorganic CEIs dominated by LiF have shown limited performance for high‐voltage LCO. Here, we propose an ionic liquid electrolyte (ILE) with a high donor number additive, enabling Li//LCO cells to achieve a high cut‐off voltage of 4.7 V/4.8 V and a high‐capacity retention of 86.9%/74.2% after 100 cycles at 0.5 C. During this process, a groundbreaking phenomenon was discovered: the construction of a stable organic CEI rich in C‐F bonds by the high donor number additive under high voltage. These strong polar C‐F bonds exhibit excellent electrochemical inertness and film‐forming properties, resulting in optimal passivation of the cathode. This organic C‐F bond‐dominated CEI significantly suppresses phase transitions, cobalt dissolution, and gas evolution in LCO at high voltage. Additionally, the 4.8 V‐class Li//LiNi0.6Co0.2Mn0.2O2 and 4.95 V‐class Li//LiNi0.5Mn1.5O4 cells also demonstrate outstanding cycling stability. Even at 60 °C, the ILE‐constructed organic CEI maintains superior performance. Our findings highlight the potential of organic CEI to enhance high‐voltage cathode stability, paving the way for more efficient lithium‐ion batteries.
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