有机自由基电池
腙
电解质
溶解
共价键
材料科学
化学工程
阴极
固态
纳米技术
电极
锂(药物)
电池(电)
化学
有机化学
物理化学
热力学
物理
工程类
内分泌学
功率(物理)
医学
作者
Xing Li,Qian Hou,Wei Huang,Hai‐Sen Xu,Xiaowei Wang,Wei Yu,Runlai Li,Kun Zhang,Lu Wang,Zhongxin Chen,Keyu Xie,Kian Ping Loh
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-10-21
卷期号:5 (11): 3498-3506
被引量:165
标识
DOI:10.1021/acsenergylett.0c01889
摘要
Solid electrolytes (SEs) are milestones in the technology roadmaps for safe and high energy density batteries. The design of organic SEs is challenged by the need to have dynamic structural fluidity for ion motion. The presence of well-ordered one-dimensional (1D) channels and stability against phase transition in covalent organic frameworks (COFs) render them potential candidates for low-temperature SEs. Herein, we demonstrate two milestones using hydrazone COF as an SE: it achieves an ion conductivity of 10–5 S cm–1 at −40 °C with a Li+ transference number of 0.92 and also prevents the dissolution of small organic molecular electrode in all-solid-state batteries. Using 1,4-benzoquinone as the cathode, a lithium battery using hydrazone COF as a SE runs for 500 cycles at a steady current density of 500 mA g–1 at 20 °C. Considering that hydrazone COF is readily amenable to large-scale production and facile post-synthetic modification, its use in an all-solid-state battery is highly promising.
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