Enhanced Surface Interactions Enable Fast Li + Conduction in Oxide/Polymer Composite Electrolyte
Enhanced Surface Interactions Enable Fast Li + Conduction in Oxide/Polymer Composite Electrolyte
复制标题
增强的表面相互作用可实现氧化物/聚合物复合电解质中的快速锂传导
DOI:
10.1002/ange.201914478
复制
发表时间:
2020
影响因子:
--
通讯作者:
Yu, Guihua
中科院分区:
文献类型:
--
作者:
Wu, Nan;Chien, Po‐Hsiu;Qian, Yumin;Li, Yutao;Xu, Henghui;Grundish, Nicholas S.;Xu, Biyi;Jin, Haibo;Hu, Yan‐Yan;Yu, Guihua
Li+‐conducting oxides are considered better ceramic fillers than Li+‐insulating oxides for improving Li+conductivity in composite polymer electrolytes owing to their ability to conduct Li+through the ceramic oxide as well as across the oxide/polymer interface. Here we use two Li+‐insulating oxides (fluorite Gd0.1Ce0.9O1.95and perovskite La0.8Sr0.2Ga0.8Mg0.2O2.55) with a high concentration of oxygen vacancies to demonstrate two oxide/poly(ethylene oxide) (PEO)‐based polymer composite electrolytes, each with a Li+conductivity above 10−4S cm−1at 30 °C. Li solid‐state NMR results show an increase in Li+ions (>10 %) occupying the more mobile A2 environment in the composite electrolytes. This increase in A2‐site occupancy originates from the strong interaction between the O2−of Li‐salt anion and the surface oxygen vacancies of each oxide and contributes to the more facile Li+transport. All‐solid‐state Li‐metal cells with these composite electrolytes demonstrate a small interfacial resistance with good cycling performance at 35 °C.