材料科学
阳极
成核
锂(药物)
电解质
共价有机骨架
化学工程
金属
吸附
枝晶(数学)
共价键
电子转移
纳米技术
无机化学
电极
物理化学
复合材料
有机化学
化学
冶金
医学
几何学
数学
多孔性
工程类
内分泌学
作者
Conghui Zhang,Jiyang Xie,Changtai Zhao,Yongxin Yang,Qi An,Zhiyuan Mei,Qijun Xu,Yuqing Ding,Genfu Zhao,Hong Guo
标识
DOI:10.1002/adma.202304511
摘要
Abstract The detrimental growth of lithium dendrites and unstable solid electrolyte interphase (SEI) inhibit the practical application of lithium‐metal batteries. Herein, atomically dispersed cobalt coordinate conjugated bipyridine‐rich covalent organic framework (sp 2 c‐COF) is explored as an artificial SEI on the surface of the Li‐metal anode to resolve these issues. The single Co atoms confined in the structure of COF enhance the number of active sites and promote electron transfer to the COF. The synergistic effects of the Co─N coordination and strong electron‐withdrawing cyano‐group can adsorb the electron from the donor (Co) at a maximum and create an electron‐rich environment, hence further regulating the Li + local coordination environment and achieving uniform Li‐nucleation behavior. Furthermore, in situ technology and density functional theory calculations reveal the mechanism of the sp 2 c‐COF‐Co inducing Li uniform deposition and promoting Li + rapid migration. Based on these advantages, the sp 2 c‐COF‐Co modified Li anode exhibits a low Li‐nucleation barrier of 8 mV, and excellent cycling stability of 6000 h.
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