材料科学
电解质
电化学窗口
纳米纤维
电化学
化学工程
热稳定性
聚合物
复合数
离子电导率
快离子导体
复合材料
电极
工程类
物理化学
化学
作者
Boyu Li,Qingmei Su,Chenchen Wu,Dong Wang,Shukai Ding,Miao Zhang,Gaohui Du,Bingshe Xu
标识
DOI:10.1021/acsami.9b14824
摘要
Using polymer electrolytes with relatively high mechanical strength, enhanced safety, and excellent flexibility to replace the conventional liquid electrolytes is an effective strategy to curb the Li-dendrite growth in Li-metal batteries (LMBs). However, low ionic conductivity, unsatisfactory thermal stability, and narrow electrochemical window still hinder their applications. Here, we fabricate Li0.35La0.55TiO3 (LLTO) nanofiber-enabled poly(vinylidene fluoride) (PVDF)-based composite polymer electrolytes (CPEs) with enhanced mechanical property and wide electrochemical window. The results show that 15 wt % of LLTO nanofibers synergize with PVDF, giving a flexible electrolyte membrane with significantly improved performance, such as high ionic conductivity (5.3 × 10–4 S cm–1), wide electrochemical window (5.1 V), high mechanical strength (stress 9.5 MPa, strain 341%), and good thermal stability (thermal degradation 410 °C). In addition, an all-solid-state Li-metal battery of sandwich-type LiFePO4/PVDF–CPE (15 wt % of LLTO)/Li delivers satisfactory cycling stability and outstanding rate performance. A reversible capacity of 121 mA h g–1 is delivered at 1 C after 100 cycles. This work exemplifies that the introduction of LLTO nanofibers can improve the electrochemical performances of PVDF-based CPEs used as electrolytes for all-solid-state LMBs.
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