电介质
电容器
俘获
材料科学
聚合物
驻极体
化学物理
解耦(概率)
储能
电荷(物理)
载流子
聚醚酰亚胺
光电子学
纳米技术
热稳定性
电场
电荷密度
原子轨道
空间电荷
静电学
高-κ电介质
工作(物理)
聚合物电容器
电荷守恒
介电强度
作者
Lu Fan,Zongliang Xie,Xi Chen,Qingsong Zhang,Yalin Wang,He Li,Xi Pang,Tiffany Chen,Shiqi Lai,Zhiyuan Huang,Ashlin M. Deatherage,Hanjiang Gu,Meng Chen,Tao Han,Liana M. Klivansky,Steve W. Shelton,Peng Liu,Zongren Peng,Ting Xu,Jian Zhang
标识
DOI:10.1002/advs.202517934
摘要
Abstract Dielectric polymer capacitors are essential for electrostatic energy storage but suffer from charge transport‐induced energy losses, particularly at elevated temperatures where thermally activated charge carriers exacerbate conduction. Conventional mitigation strategies rely on introducing heterogeneous interfaces to create charge traps, complicating scalable film fabrication. A homogeneous molecular trapping mechanism would circumvent these complexities, yet remains underexplored. Herein, a charge trapping strategy is devised by modifying the lowest occupied molecular orbitals of dielectric polymers through Lewis acid‐base adduct formation. The use of tris(pentafluorophenyl)boron (BCF) as a Lewis acidic molecular additive introduces deeper charge traps in commercial polyetherimide (PEI) while retaining homogeneity. With only 0.5 wt.% loading, the PEI‐BCF film exhibits greatly improved breakdown strength, achieving an ultrahigh discharged energy density of 7.3 J cm −3 with excellent cycle stability at 200 °C. This work establishes a facile molecular approach to decoupling charge trapping from heterogeneous interfaces, enabling high‐energy‐density polymer capacitors operable under extreme thermal conditions.
科研通智能强力驱动
Strongly Powered by AbleSci AI