材料科学
电解质
阳极
锂(药物)
枝晶(数学)
沉积(地质)
环氧乙烷
纳米技术
快离子导体
化学工程
聚合物
复合材料
电极
化学
物理化学
医学
生物
几何学
工程类
内分泌学
古生物学
数学
共聚物
沉积物
作者
Xiaofei Yang,Qian Sun,Changtai Zhao,Xuejie Gao,Keegan Adair,Yang Zhao,Jing Luo,Xiaoting Lin,Jianneng Liang,Huan Huang,Li Zhang,Shigang Lu,Ruying Li,Xueliang Sun
标识
DOI:10.1016/j.ensm.2019.07.015
摘要
Poly(ethylene oxide) (PEO) based solid polymer electrolytes (SPEs) have been regarded as promising electrolytes for next-generation all-solid-state lithium batteries (ASSLBs). However, they have achieved limited cycling stability due to their inability to suppress Li dendrite growth. Herein, a self-healing electrostatic shield (SHES) is proposed to force uniform lithium deposition by introducing 0.05 M Cs+. At this situation, the Cs+ shows a lower reduction potential compared to the Li+ reduction potential (1.7 M). During lithium deposition, the Cs+ forms a positively charged electrostatic shield around the initial Li tips, which forces further deposition of lithium to adjacent regions of the anode and results in a dendrite-free Li deposition. With this in mind, the Li–Li symmetric cells can operate for 1000 and 500 h at current densities of 0.1 and 0.2 mA cm−2, respectively, which are 10 times longer than Cs+-free PEO electrolyte. Moreover, the Li/PEO-Cs+/LiFePO4 (LFP) cell achieves high capacity retention of 90% within 100 cycles at 0.5C and retains a high capacity of 113 mAh g−1 at 0.8C, while short-circuits are observed for the Li/PEO/LFP cell, even at 0.2C. This strategy will generate substantial interest and shed light on the development of other dendrite-free SPEs and ASSLBs systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI