Rational design of all-organic flexible high-temperature polymer dielectrics

被引:27
|
作者
Wu, Chao [1 ]
Deshmukh, Ajinkya A. [2 ]
Chen, Lihua [3 ]
Ramprasad, Rampi [3 ]
Sotzing, Gregory A. [2 ,4 ]
Cao, Yang [1 ,5 ]
机构
[1] Univ Connecticut, Inst Mat Sci, Elect Insulat Res Ctr, Storrs, CT 06269 USA
[2] Univ Connecticut, Polymer Program, Storrs, CT 06269 USA
[3] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[4] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
[5] Univ Connecticut, Dept Elect & Comp Engn, Storrs, CT 06269 USA
关键词
HIGH-ENERGY-DENSITY; BREAKDOWN STRENGTH; POLYPROPYLENE; CONDUCTION;
D O I
10.1016/j.matt.2022.06.064
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Advanced polymer dielectrics are desired for high-temperature, high-density, and high-efficiency energy storage. The paradox of mutually exclusive constraints between high field endurance, dielec-tric polarization, and thermal stability amounts to a huge obstacle in the design of all-organic polymer dielectrics for safe operation un-der harsh conditions. Although there are a plethora of functional group class polymers that have been investigated and reported, there remains a large unexplored design space. A perspective of the magnitude of the grand challenge, accelerated and targeted exploration of polymer dielectrics with the rational molecular design assisted by informatics-based approaches, is presented here for the generative design and further development of poly-mers with superior thermal stability, high electric field endurance, and strong dielectric polarization.
引用
收藏
页码:2615 / 2623
页数:9
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