材料科学
氧化还原
锂(药物)
化学工程
X射线光电子能谱
阴极
聚合物
离子
有机化学
化学
物理化学
复合材料
医学
工程类
内分泌学
冶金
作者
Qiaoshuang Bai,Junlong Huang,Kehan Tang,Youlong Zhu,Dingcai Wu
标识
DOI:10.1002/adma.202416661
摘要
Abstract Redox‐active porous organic polymers (POPs) have emerged as promising and sustainable organic cathode materials (OCMs) for lithium‐ion batteries (LIBs). However, their performance is significantly limited by insufficient redox‐active sites and low intrinsic conductivity. Herein, a series of novel arylamine‐linked and bipolar POPs (denoted as HATN‐AQ, HATN‐BQ, HATN‐CBD, and HATN‐PTO) are designed and prepared as OCMs for LIBs. Benefiting from their high density of redox‐active sites, bipolar feature, and arylamine linkage, these POPs exhibited high capacity, high rate, and excellent long‐term cycling stability. Among them, HATN‐PTO displayed an ultrahigh reversible capacity of 329.6 mAh g −1 at 0.2 A g −1 with a high energy density of 716.7 Wh kg −1 , outstanding rate performance (208.7 mAh g −1 at 20 A g −1 ), and superior cycling stability (188.9 mAh g −1 capacity retained after 500 cycles at 1 A g −1 ). Furthermore, the HATN‐PTO//graphite full battery exhibited a high specific capacity of 227.3 mAh g −1 at 0.2 A g −1 and maintained a high capacity of 99.1 mAh g −1 after 200 cycles at 0.5 A g −1 . Ex situ FT‐IR and XPS spectra combined with theoretical calculations are employed to elucidate the dual‐ion storage mechanism. This work provides an effective strategy for designing POPs with high‐capacity and high‐rate for OCMs.
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