溶解度
分子间力
阴极
共轭体系
分子
材料科学
电化学
氧化还原
氢键
化学工程
无机化学
化学
电极
有机化学
物理化学
聚合物
工程类
作者
Yuxin Yao,M. Pei,Chang Su,Xin Jin,Yunpeng Qu,Zihui Song,Wanyuan Jiang,Xigao Jian,Fangyuan Hu
出处
期刊:Small
[Wiley]
日期:2024-04-15
卷期号:20 (34)
被引量:6
标识
DOI:10.1002/smll.202401481
摘要
Abstract Organic cathode materials show excellent prospects for sodium‐ion batteries (SIBs) owing to their high theoretical capacity. However, the high solubility and low electrical conductivity of organic compounds result in inferior cycle stability and rate performance. Herein, an extended conjugated organic small molecule is reported that combines electroactive quinone with piperazine by the structural designability of organic materials, 2,3,7,8‐tetraamino‐5,10‐dihydrophenazine‐1,4,6,9‐tetraone (TDT). Through intermolecular condensation reaction, many redox‐active groups C═O and extended conjugated structures are introduced without sacrificing the specific capacity, which ensures the high capacity of the electrode and enhances rate performance. The abundant NH 2 groups can form intermolecular hydrogen bonds with the C═O groups to enhance the intermolecular interactions, resulting in lower solubility and higher stability. The TDT cathode delivers a high initial capacity of 293 mAh g −1 at 500 mA g −1 and maintains 90 mAh g −1 at an extremely high current density of 70 A g −1 . The TDT || Na‐intercalated hard carbon (Na‐HC) full cells provide an average capacity of 210 mAh g −1 during 100 cycles at 500 mA g −1 and deliver a capacity of 120 mAh g −1 at 8 A g −1 .
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