电解质
材料科学
离子电导率
化学工程
复合材料
电导率
电池(电)
锚固
锂离子电池
锤子
剪切(地质)
小袋
离子键合
介孔材料
增稠
膨胀的
纳米技术
剪应力
离子
锂(药物)
容量损失
纳米颗粒
作者
Q Liu,B C Liu,K Wang,Yi Yuan,Yuxin Xia,Xin Liang,Huakun Liu,Shixue Dou,X D Li,Huaxia Deng,Xinglong Gong
出处
期刊:Small
[Wiley]
日期:2026-07-10
卷期号:22 (48): e74488-e74488
摘要
ABSTRACT The application of shear thickening electrolytes (STEs) in batteries is hindered by the conventional trade‐off, in which enhanced impact resistance comes at the cost of reduced ionic conductivity. Here, we overcome this barrier by introducing lithium sulfonate‐functionalized mesoporous silica (M‐SiO 2 ‐SO 3 Li) as a multifunctional filler. Unlike conventional fillers that impede ion transport, M‐SiO 2 ‐SO 3 Li simultaneously induces shear thickening and enhances conductivity. At 15 wt.% loading, the electrolyte achieves a remarkable ionic conductivity of 10.73 mS cm −1 , higher than that of filler‐free traditional electrolytes (TE), by anchoring anions via the ‐SO 3 Li groups to increase the Li + transference number. This synergy enables exceptional battery performance: Li||LFP cells demonstrate 97.0% capacity retention after 500 cycles, and LFP||Gr pouch full cells maintain 83.8% capacity after 200 cycles at 0.5 C. In impact tests, the robustness of this design is evident as the M‐SiO 2 ‐SO 3 Li‐based pouch cell withstands hammer drops that cause immediate failure in standard TE cells. Thus, this design strategy overcomes the performance trade‐off, integrating high conductivity, long cycling life, and impact resistance, and provides a pathway for application across the liquid‐based electrolyte family.
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