材料科学
纳米复合材料
电介质
聚合物
高-κ电介质
聚合物纳米复合材料
介电常数
介电损耗
复合材料
甲基丙烯酸甲酯
光电子学
聚合
作者
Shaobo Tu,Longguo Qiu,Chen Liu,Fanshuai Zeng,Youyou Yuan,Mohamed Nejib Hedhili,Valentina Musteaţa,Yinchang Ma,Kun Liang,Naisheng Jiang,Husam N. Alshareef,Xixiang Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-03-25
卷期号:18 (14): 10196-10205
被引量:7
标识
DOI:10.1021/acsnano.4c00475
摘要
Although numerous polymer-based composites exhibit excellent dielectric permittivity, their dielectric performance in various applications is severely hampered by high dielectric loss induced by interfacial space charging and a leakage current. Herein, we demonstrate that embedding molten salt etched MXene into a poly(vinylidene fluoride–trifluoroethylene–chlorofluoroethylene) (P(VDF–TrFE–CFE))/poly(methyl methacrylate) (PMMA) hybrid matrix induces strong interfacial interactions, forming a close-packed inner polymer layer and leading to significantly suppressed dielectric loss and markedly increased dielectric permittivity over a broad frequency range. The intensive molecular interaction caused by the dense electronegative functional terminations (−O and −Cl) in MXene results in restricted polymer chain movement and dense molecular arrangement, which reduce the transportation of the mobile charge carriers. Consequently, compared to the neat polymer, the dielectric constant of the composite with 2.8 wt % MXene filler increases from ∼52 to ∼180 and the dielectric loss remains at the same value (∼0.06) at 1 kHz. We demonstrate that the dielectric loss suppression is largely due to the formation of close-packed interfaces between the MXene and the polymer matrix.
科研通智能强力驱动
Strongly Powered by AbleSci AI