电解质
化学
阴极
氢键
分子
动力学
氢
分子间力
氢气储存
化学工程
有机分子
储能
纳米技术
材料科学
化学物理
能量密度
化学动力学
小分子
活化能
理论(学习稳定性)
电荷(物理)
作者
Weisheng Zhang,Xian‐He Chen,Chenxing Zhang,Yu‐Xuan Guo,Weikang Hu,Shilin Mei,Zi Li,Qichun Zhang,Chang‐Jiang Yao
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-09-20
卷期号:64 (45): e202515475-e202515475
被引量:10
标识
DOI:10.1002/anie.202515475
摘要
Abstract Low‐temperature energy storage systems confront severe operational constraints due to sluggish ion kinetics and electrolyte solidification. While potassium‐ion batteries (PIBs) offer potential for low‐cost energy storage, the absence of viable cathode materials with adequate stability at ultra‐low temperatures remains a critical barrier. Herein, we demonstrate an organic small molecule, 1,4‐dihydrobenzo[g]quinoxaline‐2,3,5,10‐tetraone (BQXTO), in which intermolecular hydrogen bonds (HB) and robust π─π interactions synergistically enhance charge transfer and impart insolubility, thereby facilitating reaction kinetics and improving cycling stability even under low‐temperature conditions. The assembled BQXTO||HC potassium‐ion full cell achieves remarkable energy density at −40 °C (188 Wh kg −1 ) and exceptional cyclability (88.2% capacity retention over 2000 cycles). This study presents valuable insights into the structure design of organic small molecule cathodes for advanced low‐temperature PIBs.
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