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通过设计具有单原子钴位点的共价有机框架来调控锂离子的局部配位环境以实现无枝晶锂金属电池

Regulating the Lithium Ions' Local Coordination Environment through Designing a COF with Single Atomic Co Site to Achieve Dendrite-Free Lithium-Metal Batteries.

作者信息

Zhang Conghui, Xie Jiyang, Zhao Changtai, Yang Yongxin, An Qi, Mei Zhiyuan, Xu Qijun, Ding Yuqing, Zhao Genfu, Guo Hong

机构信息

International Joint Research Center for Advanced Energy Materials of Yunnan Province, Yunnan Key Laboratory of Carbon Neutrality and Green Low-Carbon Technologies, School of Materials and Energy, Yunnan University, Kunming, 650091, China.

Solid State Batteries Research Center, GRINM (Guangdong) Institute for Advanced Materials and Technology, Foshan, Guangdong, 528051, China.

出版信息

Adv Mater. 2023 Oct;35(40):e2304511. doi: 10.1002/adma.202304511. Epub 2023 Aug 24.

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 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 c-COF-Co inducing Li uniform deposition and promoting Li rapid migration. Based on these advantages, the sp c-COF-Co modified Li anode exhibits a low Li-nucleation barrier of 8 mV, and excellent cycling stability of 6000 h.

摘要

锂枝晶的有害生长和不稳定的固体电解质界面(SEI)阻碍了锂金属电池的实际应用。在此,原子分散的钴配位富含共轭联吡啶的共价有机骨架(sp c-COF)被探索用作锂金属阳极表面的人工SEI来解决这些问题。限制在COF结构中的单个Co原子增加了活性位点的数量并促进了向COF的电子转移。Co─N配位和强吸电子氰基的协同作用可以最大程度地从供体(Co)吸附电子并创造富电子环境,从而进一步调节锂的局部配位环境并实现均匀的锂成核行为。此外,原位技术和密度泛函理论计算揭示了sp c-COF-Co诱导锂均匀沉积并促进锂快速迁移的机制。基于这些优点,sp c-COF-Co修饰的锂阳极表现出8 mV的低锂成核势垒和6000 h的优异循环稳定性。

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