Guo Can, Liu Ming, Gao Guang-Kuo, Tian Xi, Zhou Jie, Dong Long-Zhang, Li Qi, Chen Yifa, Li Shun-Li, Lan Ya-Qian
School of Chemistry, National and Local Joint Engineering Research Center of MPTES in High Energy and Safety LIBs, Engineering Research Center of MTEES (Ministry of Education), Key Lab. of ETESPG(GHEI), South China Normal University, Guangzhou, 510006, P. R. China.
Jiangsu Collaborative Innovation Centre of Biomedical Functional Materials, Jiangsu Key Laboratory of New Power Batteries, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing, 210023, P. R. China.
Angew Chem Int Ed Engl. 2022 Jan 17;61(3):e202113315. doi: 10.1002/anie.202113315. Epub 2021 Dec 3.
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.
探索共价有机框架(COF)在锂硫电池中的新应用形式,以克服其作为硫主体材料时通常存在的低导电性或高负载量(阴极中大多为≈20至≈40 wt%的负载量)等缺点,对于最大化其低密度优势以获得轻质、便携或高能量密度的器件而言是很有必要的。在此,我们证实COF作为粘结剂的微添加剂(阴极中约1 wt%)可能具有重要意义,并制备了一系列基于蒽醌-COF的中空管作为模型微添加剂。密度泛函计算证明,这些微添加剂可以增强粘结剂的基本性能,并自发地固定和催化转化多硫化锂,因此与裸电极相比,其可逆容量几乎提高了两倍。