TY - JOUR
T1 - Polyimides Physically Crosslinked by Aromatic Molecules Exhibit Ultrahigh Energy Density at 200 °C
AU - Yang, Minzheng
AU - Zhou, Le
AU - Li, Xin
AU - Ren, Weibin
AU - Shen, Yang
N1 - Publisher Copyright:
© 2023 Wiley-VCH GmbH.
PY - 2023/9/1
Y1 - 2023/9/1
N2 - Polymer dielectrics possess significant advantages in electrostatic energy storage applications, such as high breakdown strength (Eb) and efficiency (η), while their discharged energy density (Ud) at high temperature is limited by the decrease in Eb and η. Several strategies including introducing inorganic components and crosslinking have been investigated to improve the Ud of polymer dielectrics, but new issues will be encountered, e.g., the sacrifice of flexibility, the degradation of the interfacial insulating property and the complex preparation process. In this work, 3D rigid aromatic molecules are introduced into aromatic polyimides to form physical crosslinking networks through electrostatic interactions between their oppositely charged phenyl groups. The dense physical crosslinking networks strengthen the polyimides to boost the Eb, and the aromatic molecules trap the charge carriers to suppress the loss, allowing the strategy to combine the advantages of inorganic incorporation and crosslinking. This study demonstrates that this strategy is well applicable to a number of representative aromatic polyimides, and ultrahigh Ud of 8.05 J cm−3 (150 °C) and 5.12 J cm−3 (200 °C) is achieved. Furthermore, the all-organic composites exhibit stable performances during ultralong 105 charge–discharge cycles in harsh environments (500 MV m−1 and 200 °C) and prospects for large-scale preparation.
AB - Polymer dielectrics possess significant advantages in electrostatic energy storage applications, such as high breakdown strength (Eb) and efficiency (η), while their discharged energy density (Ud) at high temperature is limited by the decrease in Eb and η. Several strategies including introducing inorganic components and crosslinking have been investigated to improve the Ud of polymer dielectrics, but new issues will be encountered, e.g., the sacrifice of flexibility, the degradation of the interfacial insulating property and the complex preparation process. In this work, 3D rigid aromatic molecules are introduced into aromatic polyimides to form physical crosslinking networks through electrostatic interactions between their oppositely charged phenyl groups. The dense physical crosslinking networks strengthen the polyimides to boost the Eb, and the aromatic molecules trap the charge carriers to suppress the loss, allowing the strategy to combine the advantages of inorganic incorporation and crosslinking. This study demonstrates that this strategy is well applicable to a number of representative aromatic polyimides, and ultrahigh Ud of 8.05 J cm−3 (150 °C) and 5.12 J cm−3 (200 °C) is achieved. Furthermore, the all-organic composites exhibit stable performances during ultralong 105 charge–discharge cycles in harsh environments (500 MV m−1 and 200 °C) and prospects for large-scale preparation.
KW - aromatic molecules
KW - aromatic polyimides
KW - crosslinking
KW - electrostatic capacitors
KW - electrostatic interactions
KW - high-temperature energy storage
UR - http://www.scopus.com/inward/record.url?scp=85165248250&partnerID=8YFLogxK
U2 - 10.1002/adma.202302392
DO - 10.1002/adma.202302392
M3 - Article
AN - SCOPUS:85165248250
SN - 0935-9648
VL - 35
JO - Advanced Materials
JF - Advanced Materials
IS - 35
M1 - 2302392
ER -