journal article·2025-05-23

Soluble Semi-Alicyclic Fluorinated Copolyimide Dielectrics for High-Temperature Capacitive Energy Storage

Ling Zhou, Jinhui Song, Ganbo Liang, Shiyu Qin, Hongmei Qin, Siyu Yu, Chuanxi Xiong, Shan Wang

ACS Applied Polymer Materials· Volume 7· Issue 10
Publisher page

Abstract

Polyimides are renowned for their excellent thermal stability and insulating properties, making them ideal candidates for high-temperature dielectric energy storage. However, traditional polyimides often suffer from a narrow bandgap and limited solubility, which complicates processing and restricts their widespread application in high-performance energy storage. In this work, we propose a molecular design strategy by copolymerizing rigid, low-polarity cyclobutane-1,2,3,4-tetracarboxylic dianhydride (CBDA), 4,4′-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) with a bulky fluorinated bridge group, and 2,2′-bis(trifluoromethyl)benzidine (TFMB) to form wide-bandgap CBDA/6FDA/TFMB copolyimides, achieving a balanced performance with excellent solubility and high-temperature dielectric properties. Their electronic structure, molecular aggregation behavior, thermal stability, solubility, dielectric behavior, electrical breakdown strength, and high-temperature energy storage performance were systematically investigated as a function of 6FDA content. The results demonstrate that the copolyimide with 30% 6FDA content maintains good solubility while exhibiting excellent high-temperature dielectric polarization, low electrical conduction loss, and high breakdown strength. This leads to outstanding performance in high-temperature energy storage performance, with an energy storage density of 2.11 J/cm 3 and a charge–discharge efficiency of 90.3% at 150 °C and 350 MV/m. Overall, this work demonstrates the successful design and synthesis of semi-alicyclic fluorinated copolyimides with tailored solubility and dielectric properties, underscoring their promising potential for high-temperature dielectric energy storage applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Synthesis and properties of polymers · Dielectric materials and actuators · Silicone and Siloxane Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Materials Science and Engineering

Wuhan University of Technology

Key Laboratory of Advanced Technology for Specially Functional Materials (Ministry of Education)

Funding

Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China

References (46)

Show source-provided references
1. 10.1016/j.ensm.2021.10.01010.1016/j.ensm.2021.10.010 ↗
2. 10.1016/j.progpolymsci.2019.06.00310.1016/j.progpolymsci.2019.06.003 ↗
3. 10.1016/j.pmatsci.2016.05.00110.1016/j.pmatsci.2016.05.001 ↗
4. 10.1541/ieejfms.126.115310.1541/ieejfms.126.1153 ↗
5. 10.1038/nature1464710.1038/nature14647 ↗
6. 10.1002/smll.20220524710.1002/smll.202205247 ↗
7. 10.1021/acsami.1c0499110.1021/acsami.1c04991 ↗
8. 10.1016/j.progpolymsci.2019.01.00410.1016/j.progpolymsci.2019.01.004 ↗
9. 10.1016/j.progpolymsci.2012.02.00510.1016/j.progpolymsci.2012.02.005 ↗
10. 10.1002/adma.20200049910.1002/adma.202000499 ↗
11. 10.1016/j.pmatsci.2023.10120810.1016/j.pmatsci.2023.101208 ↗
12. 10.1002/adma.20230964010.1002/adma.202309640 ↗
13. 10.1016/j.ceramint.2024.08.23410.1016/j.ceramint.2024.08.234 ↗
14. 10.1016/j.polymer.2022.12470210.1016/j.polymer.2022.124702 ↗
15. 10.1016/j.compscitech.2020.10852810.1016/j.compscitech.2020.108528 ↗
16. 10.1038/s41467-020-17760-x10.1038/s41467-020-17760-x ↗
17. 10.1002/marc.20200001210.1002/marc.202000012 ↗
18. 10.1002/aenm.20190388110.1002/aenm.201903881 ↗
19. 10.1016/j.compscitech.2017.02.00610.1016/j.compscitech.2017.02.006 ↗
20. 10.1021/acsapm.4c0131710.1021/acsapm.4c01317 ↗
21. 10.1021/acsaem.2c0206810.1021/acsaem.2c02068 ↗
22. 10.1021/acsami.3c1873310.1021/acsami.3c18733 ↗
23. 10.1039/D3EE03644H10.1039/D3EE03644H ↗
24. 10.1016/j.compscitech.2023.11030510.1016/j.compscitech.2023.110305 ↗
25. 10.1021/acsami.3c1823710.1021/acsami.3c18237 ↗
26. 10.1039/D1MH01918J10.1039/D1MH01918J ↗
27. 10.1002/adfm.20210264410.1002/adfm.202102644 ↗
28. 10.1002/adma.20180567210.1002/adma.201805672 ↗
29. 10.1021/acsapm.4c0217910.1021/acsapm.4c02179 ↗
30. 10.1021/acs.jpcc.3c0667610.1021/acs.jpcc.3c06676 ↗
31. 10.1016/j.mtener.2022.10121710.1016/j.mtener.2022.101217 ↗
32. 10.1016/j.progpolymsci.2020.10125410.1016/j.progpolymsci.2020.101254 ↗
33. 10.1002/adma.20241092710.1002/adma.202410927 ↗
34. 10.1021/acsapm.3c0263910.1021/acsapm.3c02639 ↗
35. 10.1039/D2MH01511K10.1039/D2MH01511K ↗
36. 10.1002/pola.2840910.1002/pola.28409 ↗
37. 10.1063/5.021627210.1063/5.0216272 ↗
38. 10.1002/jcc.2288510.1002/jcc.22885 ↗
39. 10.1016/j.polymer.2021.12348810.1016/j.polymer.2021.123488 ↗
40. 10.1016/j.polymer.2007.07.01010.1016/j.polymer.2007.07.010 ↗
41. 10.1016/j.dib.2016.02.00610.1016/j.dib.2016.02.006 ↗
42. 10.1016/j.polymer.2021.12353810.1016/j.polymer.2021.123538 ↗
43. 10.1016/j.est.2024.11145810.1016/j.est.2024.111458 ↗
44. 10.1016/j.polymdegradstab.2009.11.04110.1016/j.polymdegradstab.2009.11.041 ↗
45. 10.1021/acs.chemrev.1c0079310.1021/acs.chemrev.1c00793 ↗
46. 10.1016/j.mattod.2019.04.01510.1016/j.mattod.2019.04.015 ↗