摘要
Biaxially oriented polypropylene (BOPP) are the most popular dielectric materials that used in the film capacitors products, however, the maximum operating temperature of BOPP films is only 105 °C, which limits its application in the extreme high-temperature and high-field conditions. Thus, it is urgent to develop the new-typed dielectric films with excellent energy storage performance at elevated temperature for meeting the requirements of new energy vehicles and high-voltage-direct transmission engineering. Recently, non-polar polyolefin poly (4-methyl-1-pentene) (PMP) dielectrics with superior high-temperature endurance and exhibit great potential to replace BOPP. In this work, PMP films have been successfully fabricated by melt casting technique and achieved mass-production. To further improve the high-temperature energy storage performance of PMP dielectric films, we propose a cooperative modulation of the multiscale structures including molecular chains and surfaces. In detail, UV-irradiation grafting of trifluoroethyl methacrylate (TFEMA) onto PMP molecular chains creates “bulk-traps” through polar group effects, which can effectively trap electric charges and reduce conduction loss at high-temperature. Meanwhile, the AlN/PZT heterostructured inorganic barrier layers are deposited onto the surfaces of TFEMA-grafted-PMP films via magnetron sputtering technique. The energy band structure differences between AlN/metal electrodes and AlN/PZT interfaces were utilized to construct interface barriers, thereby suppressing charge injection from metal electrodes and reducing high-temperature conduction losses. The results demonstrate that the high-temperature energy storage performances of the films have been significantly improved by optimizing UV irradiation duration and inorganic barrier layer thickness. At 150 °C, a discharged energy density of 4.23 J/cm 3 with η maintained above 91 % has been achieved, while the films exhibit excellent cycling stability of charge-discharge performances.
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