电解质
复合数
材料科学
固态
化学工程
电压
铸造
复合材料
电气工程
化学
电极
工程类
物理化学
作者
Jie Li,Liqiang Cui,Jiaxin Pang,Xue Wang,Wei Yuan,Xinlong He,Yuhang Ding,Haotian Chen,Mingfu Yu,Qiang Li,Tianyu Zhang,Hong Sun
标识
DOI:10.1021/acsaem.5c01711
摘要
Ceramic-polymer composite electrolytes represent a transformative solution for addressing safety challenges in lithium metal batteries, combining inherent nonflammability with superior ionic conductivity and dendrite-suppression properties. This study demonstrates a breakthrough in electrolyte design by developing a high-loading composite membrane containing 80 wt % Li1.3Al0.3Ti1.7(PO4)3 (LATP) within a PVDF-HFP matrix, fabricated via a simple and environmentally friendly solution-casting method. The optimized architecture features vertically aligned LATP particles creating continuous ion conduction pathways, achieving exceptional room-temperature performance: lithium ion transference number of 0.625, ionic conductivity of 5.23 × 10–4 S·cm–1, and an extended electrochemical stability window up to 5.62 V vs Li+/Li. The dual-phase design enables remarkable interfacial stability, as evidenced by stable Li plating/stripping over 500 h at 0.1 mA cm–2 in symmetric cells. When paired with LiFePO4 cathodes, full cells deliver an initial capacity of 158.64 mAh g–1 at 0.1C (25 °C) with 83.37% capacity retention after 100 cycles. This study establishes a paradigm for solid-state electrolyte engineering through synergistic microstructure control, resolving critical challenges in ceramic loading limits while maintaining interfacial compatibility - a crucial advancement toward practical high-voltage lithium metal batteries.
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