哌嗪
堆积
共价键
苯并菲
材料科学
共价有机骨架
锂(药物)
电化学
阳极
上部结构
化学工程
电极
纳米技术
无机化学
离子
有机化学
化学
物理化学
内分泌学
工程类
地质学
海洋学
医学
光电子学
液晶
作者
Rui Zhou,Yang Huang,Zhenhu Li,Shuai Kang,Xiaomin Wang,Shuangyi Liu
标识
DOI:10.1016/j.ensm.2021.05.008
摘要
The controllably spatial and chemical structures and abundantly elemental reserves of covalent organic frameworks (COFs) endow them the potential of being applied in next generation of electrochemical lithium-ions storage with high performances. Here, a piperazine-based two-dimensional covalent organic framework (PTDCOF) is designed and synthesized. PTDCOF is constructed by triphenylene units through irreversible piperazine linkages to afford the regular in-plane pores sized ~11 Å. PTDCOF is charactered with few-layered features, which is crystalized through eclipsed (AA) and staggered (AB) stacking modes together. And the synthesized framework exhibits excellent stability upon harsh chemical environments. As the active material of anodic lithium storage, the guest-eliminated product derived by PTDCOF demonstrates remarkable lithiation (1644.3 mAh g − 1 capacity contribution at 0.1 A g − 1), rate and cycling performances. The abundant active sites lead to a high and reversible lithium loading of at least 14 lithium atoms per triphenylene unit (Li14(C18N3H9)). Such product presents superior anodic lithiation capability comparing with previously reported carbonaceous materials. This study provides a possible and attractive path for hunting the high performances of lithium or other metal ions storage systems.
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