电解质
离子电导率
氧化物
离子液体
材料科学
石墨烯
环氧乙烷
结晶度
电化学
化学工程
锂(药物)
聚合物
无定形固体
无机化学
离子键合
电化学窗口
电极
离子
化学
纳米技术
有机化学
复合材料
物理化学
冶金
催化作用
内分泌学
工程类
医学
共聚物
作者
Zhongliang Hu,Xiaojing Zhang,Shimou Chen
标识
DOI:10.1016/j.jpowsour.2020.228754
摘要
Development of solid polymer electrolytes (SPEs) with superior performance is crucial for high-energy density lithium metal batteries (LMBs). Herein, a graphene oxide (GO) and ionic liquid (IL) assisted anion-immobilized polymer electrolyte (PGI) is developed, which can effectively prevent the formation of Li dendrite of LMBs. Various characterizations show that the synergetic interactions among the poly (ethylene oxide) (PEO), GO and IL in PGI, greatly reduce the crystallinity of PEO. All of the amorphous PEO, GO, and IL can effectively tether anions and enhance the ionization of lithium salts, which lead to a uniform assignment of charges and lithium ions in the electrolyte, as well as increase the transfer number of lithium ions. The PGI is utilized in all-solid-state batteries with a negligible polarization. The galvanostatic cycling tests (LiFePO4/Li cells using PGI electrolytes) at 60 °C show the initial capacities of 156.2 and 120 mAh g−1 at 0.1C and 0.5C, respectively. Moreover, the electrochemical tests also indicate that the LMBs using PGI electrolytes possess superior cycle stability at room temperature. The study provides a competitive solution for developing high-performance LMBs which can work well at both high temperature and room temperature.
科研通智能强力驱动
Strongly Powered by AbleSci AI