电解质
法拉第效率
膜
材料科学
阳极
化学工程
锂(药物)
离子电导率
化学
高分子化学
电极
聚合
复合材料
聚合物
医学
生物化学
物理化学
工程类
内分泌学
作者
Xiuli Wang,Xiaojing Hao,Hengjing Zhang,Xinhui Xia,J.P. Tu
标识
DOI:10.1016/j.electacta.2019.135108
摘要
At present, the quasi-solid-state lithium-sulfur batteries (LSBs) assembled with sulfur cathode, gel polymer electrolyte (GPE) and Li anode have explored a novel prospect for substantial energy applications owing to the high energy density and elevated security. In this work, we propose a 3D ultraviolet polymerized electrolyte, in which the inner substrate is the PEO modified PVDF-HFP electrospun membrane, and the hydrogen bonding effect plays a critical role in regulating the nanofiber diameter and membrane porosity. Simultaneously, outside coating is the in-situ ultraviolet polymerized pentaerythritol tetrakis-divinyl adipate (PETT-DA) layer, in which the carbonyl groups can effectively suppress the polysulfides shuttling. Consequently, the optimal electrolyte membranes with high porosity possess the high electrolyte uptake of 279.8%, ionic conductivity of 9.64 × 10−4 S cm−1 and Li+ transference number of 0.71 at 25 °C. Prominently, the assembled quasi-solid-state LSBs exhibit the stable coulombic efficiency of 99.5–100.0% over 300 cycles and good capacity retention of 87.1% after 300 cycles at 2C. More importantly, excellent thermal dimensional properties and mechanical performances further provide great commercial potentials for our synthesized 3D electrolyte membranes.
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