Enhanced Interfacial and Dielectric Performance for Polyetherimide Nanocomposites through Tailoring Shell Polarities
Source abstract
Abstract
Polyimide (PI) and its derivative polyetherimide (PEI) have been widely investigated as promising candidates for dielectric energy storage due to their excellent intrinsic features. However, most of the current research for PI- or PEI-based dielectric nanocomposites only focuses on a certain polar group contained in a dianhydride monomer, while there are very few studies on exploring the effect of a series of polar groups derived from various dianhydride monomers on the dielectric properties of nanocomposites. To fill this gap, we herein fabricated and investigated a series of novel hyperbranched polyimides grafted on barium titanate nanoparticles (HBPI@BT) using different dianhydride monomers and their nanocomposites with the PEI matrix. The results showed that sophisticated hyperbranched structures effectively alleviated the incompatibility between fillers and the matrix, thus significantly improving the bonding energy of nanocomposites, especially for HBPI-S@BT/PEI (797.7 kJ/mol). The U d of HBPI-S@BT/PEI reached 8.38 J/cm 3, which is 3.3 times higher than that of pure PEI. The HBPI-F@BT/PEI nanocomposites achieved high breakdown strength (∼500 MV/m) and low dielectric loss (0.008) simultaneously. The dielectric constants of HBPI@BT/PEI nanocomposites remained at a stable level from 25 to 150 °C. This work provides us promising hyperbranched structured materials for potentially advanced dielectric applications such as field effect transistors.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Dielectric materials and actuators · Synthesis and properties of polymers · Ferroelectric and Piezoelectric Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Specially Functional Polymeric Materials and Related Technology (Ministry of Education), School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China
Funding
Natural Science Foundation of Shanghai · Science and Technology Commission of Shanghai Municipality · Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China
References (51)
Show source-provided references
1. 10.1016/j.nanoen.2021.10643810.1016/j.nanoen.2021.106438 ↗
2. 10.1002/adfm.20180856710.1002/adfm.201808567 ↗
3. 10.1016/j.matdes.2020.10848610.1016/j.matdes.2020.108486 ↗
4. 10.1146/annurev-matsci-070214-02101710.1146/annurev-matsci-070214-021017 ↗
5. 10.1016/j.cej.2021.12847610.1016/j.cej.2021.128476 ↗
6. 10.1016/j.pmatsci.2020.10067010.1016/j.pmatsci.2020.100670 ↗
7. 10.1002/advs.20210222110.1002/advs.202102221 ↗
8. 10.1016/j.nanoen.2020.10541210.1016/j.nanoen.2020.105412 ↗
9. 10.1039/C7TA00136C10.1039/C7TA00136C ↗
10. 10.1002/advs.20170051210.1002/advs.201700512 ↗
11. 10.1039/D2TC00153E10.1039/D2TC00153E ↗
12. 10.1002/advs.20210577310.1002/advs.202105773 ↗
13. 10.1016/j.compscitech.2020.10834110.1016/j.compscitech.2020.108341 ↗
14. 10.1021/acs.macromol.1c0077810.1021/acs.macromol.1c00778 ↗
15. 10.1039/D0CP05233G10.1039/D0CP05233G ↗
16. 10.1039/C7PY01914A10.1039/C7PY01914A ↗
17. 10.1021/cm401048610.1021/cm4010486 ↗
18. 10.1016/j.cej.2019.02.10610.1016/j.cej.2019.02.106 ↗
19. 10.1016/j.ceramint.2022.04.01710.1016/j.ceramint.2022.04.017 ↗
20. 10.1016/j.matlet.2021.12943410.1016/j.matlet.2021.129434 ↗
21. 10.1039/D0CS00765J10.1039/D0CS00765J ↗
22. 10.1021/acsapm.0c0114110.1021/acsapm.0c01141 ↗
23. 10.1021/nn304414810.1021/nn3044148 ↗
24. 10.1039/C7TA00587C10.1039/C7TA00587C ↗
25. 10.1016/j.mtener.2022.10115810.1016/j.mtener.2022.101158 ↗
26. 10.1016/j.jpowsour.2022.23141510.1016/j.jpowsour.2022.231415 ↗
27. 10.1016/j.matt.2022.06.06410.1016/j.matt.2022.06.064 ↗
28. 10.1002/adfm.20210264410.1002/adfm.202102644 ↗
29. 10.1039/C8TC04510K10.1039/C8TC04510K ↗
30. 10.1039/D1TA08855F10.1039/D1TA08855F ↗
31. 10.1002/adma.20130175210.1002/adma.201301752 ↗
32. 10.1002/adma.20200819810.1002/adma.202008198 ↗
33. 10.1016/j.pmatsci.2018.10.00310.1016/j.pmatsci.2018.10.003 ↗
34. 10.1002/adma.20160172710.1002/adma.201601727 ↗
35. 10.1039/D1EE03186D10.1039/D1EE03186D ↗
36. 10.1038/s41467-020-17760-x10.1038/s41467-020-17760-x ↗
37. 10.1016/j.progpolymsci.2020.10125410.1016/j.progpolymsci.2020.101254 ↗
38. 10.1016/j.matt.2021.04.02610.1016/j.matt.2021.04.026 ↗
39. 10.1016/j.matdes.2020.10933510.1016/j.matdes.2020.109335 ↗
40. 10.1016/j.apsusc.2022.15399110.1016/j.apsusc.2022.153991 ↗
41. 10.1016/j.ensm.2019.12.00610.1016/j.ensm.2019.12.006 ↗
42. 10.1016/j.nanoen.2018.03.04910.1016/j.nanoen.2018.03.049 ↗
43. 10.1039/C4TA01818D10.1039/C4TA01818D ↗
44. 10.1021/am100146u10.1021/am100146u ↗
45. 10.1016/j.compscitech.2020.10850110.1016/j.compscitech.2020.108501 ↗
46. 10.1016/j.ensm.2019.10.01610.1016/j.ensm.2019.10.016 ↗
47. 10.1016/j.apsusc.2018.07.12810.1016/j.apsusc.2018.07.128 ↗
48. 10.1016/j.est.2022.10516310.1016/j.est.2022.105163 ↗
49. 10.1016/j.apsusc.2017.07.14910.1016/j.apsusc.2017.07.149 ↗
50. 10.1016/j.ceramint.2016.11.12810.1016/j.ceramint.2016.11.128 ↗
51. 10.1021/acsami.8b0112910.1021/acsami.8b01129 ↗