材料科学
聚酰亚胺
阴极
聚合物
锂(药物)
氧化还原
单体
化学工程
电极
共轭体系
纳米技术
复合材料
物理化学
图层(电子)
化学
医学
内分泌学
工程类
冶金
作者
Pengfei Xu,Feng Gao,Dong Liu
标识
DOI:10.1002/admi.202300464
摘要
Abstract Organic polymers are promising candidates as cathode materials for lithium storage, however, suffer from low theoretical capacity due to the presence of multiple inactive components in the polymers. Herein, a novel hexaazatriphenylene‐based polyimide with high theoretical capacity (436 mAh g −1 ) is developed via the precise design of monomers and controllable synthesis of corresponding polymers. The as‐prepared polymers possess rich edge pyrazine nitrogen (C═N) and carbonyl groups (C═O), well‐defined porosity, and conjugated structure, benefiting for high capacity, rapid ion and charge transport. The resultant polymers electrode achieves a high specific capacity of 303 mAh g −1 at 100 mA g −1 , high‐rate capability (171 mAh g −1 even at 8 C, 1 C = 400 mA g −1 ), and stable cycle performance with a high capacity retention of 93.8% at 500 mA g −1 over 200 cycles. Combined experimental and theoretical calculations reveal that both C═O and C═N sites in the polyimide are served as redox sites for lithium storage, providing high specific capacity. This work offers a novel approach for the development of polymeric cathode materials with dense redox sites for next‐generation energy‐dense batteries.
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