Significantly enhancing the dielectric constant and breakdown strength of linear dielectric polymers by utilizing ultralow loadings of nanofillers

被引:75
|
作者
Li, Li [1 ,2 ]
Cheng, Jingsai [3 ]
Cheng, Yunyun [1 ]
Han, Ting [1 ]
Liu, Yang [2 ]
Zhou, Yao [2 ]
Han, Zhubing [2 ]
Zhao, Guanghui [3 ]
Zhao, Yan [3 ]
Xiong, Chuanxi [1 ]
Dong, Lijie [1 ]
Wang, Qing [2 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Ctr Smart Mat & Devices, Wuhan 430070, Hubei, Peoples R China
[2] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
[3] Wuhan Univ Technol, Res Ctr Mat Genome Engn, Int Mat Sci & Engn, Wuhan 430070, Hubei, Peoples R China
基金
国家重点研发计划;
关键词
ENERGY-STORAGE PERFORMANCE; LOW ELECTRIC-FIELDS; DISCHARGE EFFICIENCY; QUANTUM DOTS; NANOCOMPOSITES; DENSITY; CHARGE; FILMS; SIZE; POLYPROPYLENE;
D O I
10.1039/d1ta05408b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Dielectric polymers with high electrostatic energy storage capability are the enabling technology for advanced electronics and electric power systems. However, the development of dielectric polymers is rather limited by their undesired discharged energy density (U-e) due to the intrinsic low dielectric constant (K). Although large improvements of K can be achieved in dielectric polymers by introducing high filling ratios (>10 vol%) of high-K inorganic fillers, this approach has had only limited success in enhancing energy density due to the negative impact on the breakdown strength (E-b) and charge-discharge efficiency (eta). Herein, we report that the incorporation of ultralow amounts (<1 vol%) of low-K quantum dot (QD) nanofillers into a linear polymer leads to pronounced and concurrent enhancements in both K and E-b, yielding a high U-e of 17.6 J cm(-3) with an eta of >87% at 800 MV m(-1). The improvement ratios of K (similar to 69%) and E-b (similar to 60%) reported in this work represent the record values in linear dielectric polymer composites with low filler content (<= 5 vol%). The observed dielectric enhancement is rationalized by the significant contributions of the interface including enhanced polymer chain mobility and induced interfacial dipoles as revealed in the interphase dielectric model and interface simulations based on density functional theory (DFT). The improved mechanical strength and raised interface charge barriers are responsible for the high E-b. This contribution paves a new avenue for designing scalable polymer-based dielectric materials exhibiting high energy densities and efficiencies and provides fundamental insights into the dielectric behaviors at the interfaces in polymer nanocomposites.
引用
收藏
页码:23028 / 23036
页数:9
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