材料科学
电解质
离子键合
锂(药物)
离子电导率
离解(化学)
共价有机骨架
离子
共价键
化学工程
纳米技术
化学物理
电极
物理化学
化学
有机化学
多孔性
医学
工程类
复合材料
内分泌学
作者
Guoxing Jiang,Wenwu Zou,Weifeng Zhang,Zhaoyuan Ou,Shengguang Qi,Tongmei Ma,Zhiming Cui,Zhenxing Liang,Li Du
标识
DOI:10.1002/aenm.202303672
摘要
Abstract Rational regulation of the Li‐ion (Li + ) migration behaviors and charge distribution at the electrolyte–electrode interface is of great significance in pursuit of high‐performance lithium metal battery (LMB) chemistry. Herein, unique locally‐zwitterionic covalent organic framework nanosheets (ziCOFNs) are developed as Li + accelerated regulators, whose functions include not only kinetics‐boosted Li + migration but also induces uniform charge distribution in LMBs. The zwitterions act as “dissociation enhancers” to trigger efficient Li + desolvation, while the abundant ─COO − units within the nanopores favor rapid Li + diffusion. In addition, the ordered ionic skeleton dynamically homogenizes the interfacial charge, thereby inhibiting Li dendrite growth and stabilizing the Li‐interface chemistry. When implemented as a functional interlayer in the cell configuration, ziCOFNs display ultrahigh transfer number (0.84) and ionic conductivity beyond 4.5 mS cm −1 . With such a layer, stable Li plating/stripping (over 6500 h) at 3 mA cm −2 in symmetric cells, and superior long‐term cycle performance in high‐loading LiFePO 4 (9.4 mg cm −2 ) full cells are achieved. Detailed experimental characterizations combined with theoretical calculations elucidate the mechanism of the zwitterionic framework tuning Li + migration behaviors. This work is anticipated to shed fresh light on the exploration of zwitterionic crystalline materials in next‐generation LMBs.
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