Significantly Enhanced High-Temperature Energy Storage Properties of Poly(ether imide) Dielectrics Enabled by Ultralow Content of Ni@Al 2 O 3 Nanofibers
Source abstract
Abstract
Polymer dielectrics play an indispensable role in electrostatic energy storage due to their merits of high voltage resistance, lightweight, excellent flexibility, and easy processability. However, the deterioration in dielectric reliability and energy loss at high temperatures limit their versatility for broader applications. Herein, Ni@Al 2 O 3 NFs are fabricated by encapsulating different content of nickel (Ni) nanoparticles into alumina nanofibers (Al 2 O 3 NFs) via the electrospinning technique and employed to simultaneously improve the dielectric constant and breakdown strength of poly(ether imide) (PEI). This is realized by the coupling action of the increased interfacial polarization, Coulomb blockade effect of Ni nanoparticles, and wide bandgap of Al 2 O 3 NFs. Notably, the PEI nanocomposite films containing 0.50 vol % Ni@Al 2 O 3 NFs exhibit an excellent discharge energy density ( U d ) of 5.8 J/cm 3 at 150 °C, 262% higher than that of pristine PEI ( U d = 1.6 J/cm 3 ), accompanied by a high efficiency of 81.3%. This work provides a promising strategy to improve the high-temperature energy storage performance of polymer-based dielectrics by exerting the synergistic effect of fillers at ultralow content.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Dielectric materials and actuators · Synthesis and properties of polymers · High voltage insulation and dielectric phenomena
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Material Science and Chemical Engineering
Harbin University of Science and Technology
Key Laboratory of Engineering Dielectric and Its Application, Ministry of Education
Funding
Key Technology Research and Development Program of Shandong Province
References (43)
Show source-provided references
1. 10.1038/s41565-023-01541-w10.1038/s41565-023-01541-w ↗
2. 10.1126/science.adl293110.1126/science.adl2931 ↗
3. 10.1021/acs.chemrev.1c0079310.1021/acs.chemrev.1c00793 ↗
4. 10.1080/15583724.2021.191760910.1080/15583724.2021.1917609 ↗
5. 10.1016/j.joule.2022.12.01010.1016/j.joule.2022.12.010 ↗
6. 10.1039/D4SC05437G10.1039/D4SC05437G ↗
7. 10.1016/j.progpolymsci.2025.10193110.1016/j.progpolymsci.2025.101931 ↗
8. 10.1002/smll.20230431010.1002/smll.202304310 ↗
9. 10.1039/D3TC04715F10.1039/D3TC04715F ↗
10. 10.1016/j.cej.2025.16079310.1016/j.cej.2025.160793 ↗
11. 10.1002/adma.20241565210.1002/adma.202415652 ↗
12. 10.1039/D0CS00765J10.1039/D0CS00765J ↗
13. 10.1021/acs.jpclett.3c0283210.1021/acs.jpclett.3c02832 ↗
14. 10.1021/acsami.3c0677810.1021/acsami.3c06778 ↗
15. 10.1016/j.compscitech.2022.10942110.1016/j.compscitech.2022.109421 ↗
16. 10.1016/j.est.2023.10954010.1016/j.est.2023.109540 ↗
17. 10.1016/j.compscitech.2023.11030510.1016/j.compscitech.2023.110305 ↗
18. 10.1038/s41467-020-17760-x10.1038/s41467-020-17760-x ↗
19. 10.1002/adfm.20221005010.1002/adfm.202210050 ↗
20. 10.1063/5.019032310.1063/5.0190323 ↗
21. 10.1016/j.compscitech.2020.10850110.1016/j.compscitech.2020.108501 ↗
22. 10.1007/s12598-022-02241-510.1007/s12598-022-02241-5 ↗
23. 10.1002/smll.20220242110.1002/smll.202202421 ↗
24. 10.1002/adfm.20220415510.1002/adfm.202204155 ↗
25. 10.1016/j.compositesa.2020.10626610.1016/j.compositesa.2020.106266 ↗
26. 10.1021/acsami.3c1773510.1021/acsami.3c17735 ↗
27. 10.1016/j.cej.2024.15477910.1016/j.cej.2024.154779 ↗
28. 10.1039/D2TC00968D10.1039/D2TC00968D ↗
29. 10.1039/D4MH00299G10.1039/D4MH00299G ↗
30. 10.1016/j.ceramint.2024.08.23410.1016/j.ceramint.2024.08.234 ↗
31. 10.1002/adma.20170438010.1002/adma.201704380 ↗
32. 10.1515/epoly.2009.9.1.125010.1515/epoly.2009.9.1.1250 ↗
33. 10.1002/pi.301010.1002/pi.3010 ↗
34. 10.1016/j.apsusc.2020.14587710.1016/j.apsusc.2020.145877 ↗
35. 10.1039/D1RA01570B10.1039/D1RA01570B ↗
36. 10.1103/PhysRevB.86.11511710.1103/PhysRevB.86.115117 ↗
37. 10.1038/nature1464710.1038/nature14647 ↗
38. 10.1016/j.cej.2025.16106310.1016/j.cej.2025.161063 ↗
39. 10.1063/5.014587910.1063/5.0145879 ↗
40. 10.1016/j.compscitech.2020.10852810.1016/j.compscitech.2020.108528 ↗
41. 10.1002/admi.20220110010.1002/admi.202201100 ↗
42. 10.1016/j.cej.2022.14095010.1016/j.cej.2022.140950 ↗
43. 10.1007/s10118-024-3068-x10.1007/s10118-024-3068-x ↗