摘要
Covalent organic frameworks(COFs), as highly tunable porous crystalline materials, have promising applications in potassium-ion batteries(PIBs) due to their abundant charge carrier transport channels and excellent structural stability. However, the excessive stacking of interlayer electron clouds makes it difficult to expose internal active sites. Strategies to design functional COFs with controllable morphology and copious active sites are promising but still challenging. Herein, by utilizing the condensation between1,3,5-triformylbenzene(TFB) and p-phenylenediamine(PPD) and using amino-modified SiO_(2) nanospheres as templates, we synthesize core-shell NH_(2)-SiO_(2)@TP-COF. Through NaOH etching of NH_(2)-SiO_(2)@TP-COF, we obtain imine-based TP-COF hollow nanospheres, which shows excellent potassium storage performance when applied to the anode for PIBs. Ex-situ analysis and density functional theory calculations reveal that C=N groups and benzenes are active sites for K^(+) storage.
基金
supported by the National Natural Science Foundation of China (No. 22179063)。