阴极
材料科学
共价有机骨架
锂(药物)
电导率
化学工程
电极
密度泛函理论
蒽醌
能量密度
纳米技术
硫黄
共价键
化学
有机化学
物理化学
冶金
计算化学
工程物理
内分泌学
工程类
医学
作者
Can Guo,Ming Liu,Guang‐Kuo Gao,Xi Tian,Jie Zhou,Long‐Zhang Dong,Qi Li,Yifa Chen,Shunli Li,Ya‐Qian Lan
标识
DOI:10.1002/ange.202113315
摘要
Abstract The exploration of new application forms of covalent organic frameworks (COFs) in Li−S batteries that can overcome drawbacks like low conductivity or high loading when typically applied as sulfur host materials (mostly ≈20 to ≈40 wt % loading in cathode) is desirable to maximize their low‐density advantage to obtain lightweight, portable, or high‐energy‐density devices. Here, we establish that COFs could have implications as microadditives of binders (≈1 wt % in cathode), and a series of anthraquinone‐COF based hollow tubes have been prepared as model microadditives. The microadditives can strengthen the basic properties of the binder and spontaneously immobilize and catalytically convert lithium polysulfides, as proved by density functional calculations, thus showing almost doubly enhanced reversible capacity compared with that of the bare electrode.
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