金属锂
成核
枝晶(数学)
阳极
沉积(地质)
材料科学
寄主(生物学)
锂(药物)
金属
共价键
纳米技术
化学工程
化学
电极
冶金
生物
有机化学
生态学
数学
工程类
古生物学
物理化学
内分泌学
几何学
沉积物
作者
Yun‐Wei Song,Peng Shi,Bo‐Quan Li,Xiang Chen,Zhao Chang-xin,Weijing Chen,Xue‐Qiang Zhang,Xiao Chen,Qiang Zhang
出处
期刊:Matter
[Elsevier BV]
日期:2020-11-05
卷期号:4 (1): 253-264
被引量:89
标识
DOI:10.1016/j.matt.2020.10.014
摘要
Summary Lithium (Li) metal represents one of the most promising anode materials for constructing high-energy-density rechargeable batteries. However, uncontrolled Li dendrite growth induces limited lifespan and safety hazards, impeding the development of Li metal batteries severely. Introducing a Li host has been shown to effectively relieve dendrite growth, while further construction of lithiophilic sites will significantly facilitate uniform Li deposition for stably cycling Li metal batteries. Herein, a boroxine covalent organic framework (COF-1) is employed to construct a lithiophilic host for dendrite inhibition in working Li metal batteries. The well-defined boroxine sites demonstrate ideal lithiophilicity to reduce the Li nucleation energy barrier, and the ordered framework structure of COF-1 affords a uniform distribution of the lithiophilic sites. As a result, the COF-1-based Li host affords a more than doubled lifespan of routine anodes in both half- and full cells. This work demonstrates the promising potential of applying advanced framework materials to essential energy-related processes.
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