材料科学
电介质
电容感应
共聚物
平面的
电容
聚丙烯
光电子学
介电强度
介电常数
储能
化学工程
泄漏(经济)
工作(物理)
电荷密度
带隙
介电损耗
二胺
电荷(物理)
高分子化学
功率密度
电流密度
化学物理
凝聚态物理
复合材料
活化能
电场
俘获
作者
Tan Li,Ding Ai,Wugang Liao,Shuangwu Huang,Qiyan Zhang
标识
DOI:10.1021/acs.jpclett.6c02606
摘要
Abstract Poly(ether imide) (PEI) is a promising high-temperature dielectric material, yet its application is limited by severe intrachain and interchain charge transfer (CT) effects, which give rise to high leakage currents at elevated temperatures. Tuning interchain spacing has been recognized as an effective strategy to suppress CT effects, but it entails an intrinsic tradeoff: excessively large spacing facilitates free charge transport, whereas overly compact chain packing exacerbates CT interactions. Herein, we report a series of spiral-twisted PEI copolymers synthesized by incorporating the bulky, twisted BAFL diamine and the planar PPDA diamine with BPADA dianhydride. By systematically varying the BAFL/PPDA molar ratio, we identified that the cPEI-5 composition (50 mol % BAFL and 50 mol % PPDA) as possessing the most favorable interchain spacing, which effectively suppresses CT without unduly weakening interchain coupling, thereby yielding the widest bandgap (3.37 eV) and the deepest trap level (2.19 eV). This optimal spacing, enabled by the spiral-twisted backbone, concurrently shortens the hopping distance and lowers the carrier mobility, leading to a substantial reduction in leakage current. Consequently, cPEI-5 achieves a breakdown strength of 610 MV m–1 at 150 °C, which is 36.2% higher than cPEI-0 and 9.5% higher than cPEI-10, and delivers a discharged energy density of 5.5 J cm–3 at > 90% efficiency, surpassing the room-temperature performance of biaxially oriented polypropylene (BOPP, 4.0 J cm–3). Moreover, cPEI-5 demonstrates excellent cycling stability (over 50 000 cycles, 0.8% loss) and fast discharge capability (t95 = 2.47 μs, power density = 0.28 MW cm–3). This work underscores that rational engineering of spiral-twisted structures enables a synergistic balance between CT suppression and charge transport, offering a new paradigm for high-performance polymer dielectrics under harsh operating conditions.
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