环氧乙烷
电解质
阳极
材料科学
法拉第效率
钙钛矿(结构)
复合数
电导率
氧化物
离子电导率
聚合物
无机化学
化学工程
快离子导体
锂(药物)
复合材料
化学
冶金
物理化学
电极
工程类
内分泌学
共聚物
医学
作者
Henghui Xu,Po‐Hsiu Chien,Jianjian Shi,Yutao Li,Nan Wu,Yuanyue Liu,Yan‐Yan Hu,John B. Goodenough
标识
DOI:10.1073/pnas.1907507116
摘要
Flexible and low-cost poly(ethylene oxide) (PEO)-based electrolytes are promising for all-solid-state Li-metal batteries because of their compatibility with a metallic lithium anode. However, the low room-temperature Li-ion conductivity of PEO solid electrolytes and severe lithium-dendrite growth limit their application in high-energy Li-metal batteries. Here we prepared a PEO/perovskite Li3/8Sr7/16Ta3/4Zr1/4O3 composite electrolyte with a Li-ion conductivity of 5.4 × 10-5 and 3.5 × 10-4 S cm-1 at 25 and 45 °C, respectively; the strong interaction between the F- of TFSI- (bis-trifluoromethanesulfonimide) and the surface Ta5+ of the perovskite improves the Li-ion transport at the PEO/perovskite interface. A symmetric Li/composite electrolyte/Li cell shows an excellent cyclability at a high current density up to 0.6 mA cm-2 A solid electrolyte interphase layer formed in situ between the metallic lithium anode and the composite electrolyte suppresses lithium-dendrite formation and growth. All-solid-state Li|LiFePO4 and high-voltage Li|LiNi0.8Mn0.1Co0.1O2 batteries with the composite electrolyte have an impressive performance with high Coulombic efficiencies, small overpotentials, and good cycling stability.
科研通智能强力驱动
Strongly Powered by AbleSci AI