Abstract
Dielectric polymers that can withstand harsh conditions of simultaneous high electric field and elevated temperature are widely used in electrical and electronic systems. However, traditionally, the thermal stability of polymers is engineered based on highly conjugated aromatic molecular structures, giving rise to soring charge transport and thus poor charge–discharge efficiency under concurrent high electric field and elevated temperature. Here, we locally improved the rotational flexibility of the phenylenediamine linkage structure in polyetherimide (PEI) to decouple the conjugation of the organic molecule. p-Phenylenediamine (5 mol %) as a low-energy rotation repeat unit within PEI significantly optimized its dielectric properties, exhibiting substantially suppressed electrical conduction (more than 1 order of magnitude lower) and polarization loss (<1%). The new PEI has a largely improved charge–discharge efficiency of 91% at 400 MV/m 200 °C, outperforming the best-reported polymer-based dielectrics without any modification of the cost of goods. The high-throughput facile processing of the new PEI provides a potential candidate for energy storage applications under elevated temperatures. This work unveils a scalable approach to exploring polymer dielectrics by introducing a small amount of local structural modifications.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.