电解质
溶剂化
电化学
石墨
离子
电极
化学
化学工程
材料科学
锂(药物)
自行车
工作(物理)
相容性(地球化学)
化学稳定性
无机化学
丙酸盐
化学物理
纳米技术
储能
离子键合
分子动力学
金属锂
隐溶剂化
溶剂化壳
作者
Yi Li,Zheng Ma,Pushpendra Kumar,Honghong Liang,Fei Zhao,Akang Huang,Jia Wang,Wandi Wahyudi,Hui Zhu,Jiao Yin,Hongliang Xie,Qian Li,Jun Ming
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-10-09
卷期号:10 (11): 5345-5355
被引量:3
标识
DOI:10.1021/acsenergylett.5c02695
摘要
Lithium-ion batteries (LIBs) face challenges in the stability and electrode compatibility of conventional electrolytes at high voltages and extreme temperatures. Here, we present an electrolyte design featuring a moderately dissociating solvation structure, achieved by combining lithium difluoro(oxalato)borate (LiDFOB) with ethyl propionate (EP). This formulation promotes the formation of abundant contact ion pairs (CIPs), which effectively weaken Li + –solvent interactions, enhance oxidative stability, and lower Li + desolvation energy. As a result, graphite || LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811) full cells deliver outstanding long-term cycling stability at 4.5 V (vs Li/Li + ) across a wide temperature range, retaining 94.2% capacity after 300 cycles at −20 °C and 92.5% after 100 cycles at 60 °C. An interfacial model reveals how the optimized solvation structure, governed by moderately dissociating Li + –anion interactions, enhances interfacial stability and cycling performance under demanding conditions. This work underscores the pivotal role of solvation structure engineering in advancing electrolyte stability in next-generation LIBs.
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