材料科学
电解质
电化学
电化学窗口
离子电导率
锂(药物)
电池(电)
阳极
聚合物
化学工程
快离子导体
有机自由基电池
热稳定性
电极
复合材料
化学
工程类
内分泌学
物理
物理化学
功率(物理)
医学
量子力学
作者
Dong‐Myeong Shin,Jonathan E. Bachman,Mercedes K. Taylor,Jovan Kamcev,Jesse G. Park,Michael E. Ziebel,Ever O. Velasquez,Nanette N. Jarenwattananon,Gurmukh K. Sethi,Yi Cui,Jeffrey R. Long
标识
DOI:10.1002/adma.201905771
摘要
Lithium-ion batteries have remained a state-of-the-art electrochemical energy storage technology for decades now, but their energy densities are limited by electrode materials and conventional liquid electrolytes can pose significant safety concerns. Lithium metal batteries featuring Li metal anodes, solid polymer electrolytes, and high-voltage cathodes represent promising candidates for next-generation devices exhibiting improved power and safety, but such solid polymer electrolytes generally do not exhibit the required excellent electrochemical properties and thermal stability in tandem. Here, an interpenetrating network polymer with weakly coordinating anion nodes that functions as a high-performing single-ion conducting electrolyte in the presence of minimal plasticizer, with a wide electrochemical stability window, a high room-temperature conductivity of 1.5 × 10-4 S cm-1 , and exceptional selectivity for Li-ion conduction (tLi+ = 0.95) is reported. Importantly, this material is also flame retardant and highly stable in contact with lithium metal. Significantly, a lithium metal battery prototype containing this quasi-solid electrolyte is shown to outperform a conventional battery featuring a polymer electrolyte.
科研通智能强力驱动
Strongly Powered by AbleSci AI