Inhibition conduction loss for distinct improvement of energy storage density over a broad temperature range in polyetherimide-based composite films

被引:7
|
作者
Chen, Hanxi [1 ]
Pan, Zhongbin [1 ]
Cheng, Yu [1 ]
Ding, Xiangping [1 ]
Li, Zhicheng [1 ]
Fan, Xu [1 ]
Liu, Jinjun [1 ]
Li, Peng [2 ]
Yu, Jinhong [3 ]
Zhai, Jiwei [4 ]
机构
[1] Ningbo Univ, Sch Mat Sci & Chem Engn, Ningbo 315211, Zhejiang, Peoples R China
[2] Liaocheng Univ, Sch Mat Sci & Engn, Liaocheng 252059, Peoples R China
[3] Univ Chinese Acad Sci, Chinese Acad Sci, Ningbo Inst Mat, Key Lab Marine Mat & Related Technol,Zhejiang Key, Ningbo 315201, Zhejiang, Peoples R China
[4] Tongji Univ, Sch Mat Sci & Engn, 4800 Caoan Rd, Shanghai 201804, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymer nanocomposites; Sandwich structure; High; -temperature; Energy storage; Capacitors; STRUCTURED POLYMER NANOCOMPOSITES; DIELECTRIC MATERIALS; DISCHARGE EFFICIENCY; POLYPROPYLENE;
D O I
10.1016/j.polymer.2022.125572
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The exploration of high-energy-density polymer dielectrics that can operate stably under high temperatures is of great significance in order to meet the growing needs for modern high-power electronics. However, the drasti-cally deteriorated capacitive performances brought by the inevitable conduction loss at elevated temperature grievously hinder their application in extreme circumstances. Herein, a class of sandwich-structured dielectric nanocomposites capitalizing on binary wide-bandgap nanofillers is reported. The synergy of wide bandgap Al2O3 nanoparticles and hydroxyl-modified BNNSs can build higher interfacial barrier to efficiently depress the thermionic charge injection and carrier transport in dielectrics, yielding a substantially inhibited electrical conduction of the composites under elevated temperature. Indeed, the resulting sandwich-structured polymer composites deliver first-class-level discharged energy density (Ud) of-2.23 J/cm3 with efficiency (eta) > 90% even under the ultra-high temperature of 200 degrees C, which is by far the current free-standing high-temperature dielectric polymer and polymer-based composites reported to date. Together with remarkable dielectric stability over a wide temperature and frequency range and outstanding cyclability, this contribution puts forward an efficient approach to groping for scalable high-temperature dielectric polymer nanocomposites for advanced electrical energy storage.
引用
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页数:9
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