聚酰亚胺
材料科学
极地的
电场
电子
电子转移
光电子学
化学物理
储能
泄漏(经济)
密度泛函理论
亚苯基
电子密度
电子迁移率
纳米技术
电子传输链
电流密度
电压
化学极性
化学工程
高分子化学
电子供体
作者
Jiaqi Zhang,Qiyue Zhang,Tiandong Zhang,Yongquan Zhang,Yue Zhang,Changhai Zhang,Tongqin Zhang,Xu Tong,Qingguo Chi,Jiaqi Zhang,Qiyue Zhang,Tiandong Zhang,Yongquan Zhang,Yue Zhang,Changhai Zhang,Tongqin Zhang,Xu Tong,Qingguo Chi
标识
DOI:10.1002/adfm.202518827
摘要
Abstract The strong conjugation effect in homogeneous phenylene polyimide exhibits remarkable electron transfer characteristics, leading to significant leakage currents, which severely constrain the energy storage performance of polyimide. However, the electron transfer mechanism of polyimide under high electric fields remains unclear, and the influence mechanisms of polar group modifications at different positions on the intrinsic electron transfer properties of polyimide still require further investigation. To address the aforementioned key issues, this study systematically investigates the regulatory mechanisms of polar groups and their positions on the electron transfer properties of polyimide by combining theoretical calculations with experimental validation. DFT computational results indicate that introducing highly polar groups into the donor structure of polyimide can effectively reduce the electrostatic potential difference induced by conjugation and enhance the localization characteristics of electron transfer. Moreover, experimental test results are highly consistent with theoretical predictions. The polyimide incorporating sulfonyl groups into its donor structure with leakage current density significantly reduce to 1.66 × 10 −10 A cm −2 , and demonstrate outstanding high‐temperature energy storage performance. At 150 °C, the discharge energy density substantially increases to 4.70 J cm −3 , representing an impressive 310.5% improvement over conventional PI. This study provides crucial theoretical foundations and practical guidance for developing high‐performance polyimide energy storage materials.
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