journal article·2022-12

Annealed Covalent Organic Framework Thin Films for Exceptional Absorption of Ultrabroad Low‐Frequency Electromagnetic Waves

Yaling Li, Xinpei Gao, Ming Wang, Yanan Gao, Donglin Jiang

Small· Volume 18· Issue 50
Publisher page

Abstract

Abstract Different from harvesting of ultraviolet and visible lights via electronic transitions, absorption of low‐frequency electromagnetic waves is sophisticated in mechanism and poor in efficiency, imposing the structural design arduous and challenging. Here, the first example of exploring covalent organic frameworks for highly efficient absorption of low‐frequency electromagnetic waves is reported. Three pyrene frameworks are synthesized and annealed into porous networks, which upon mixture with paraffin are processed into thin films with tunable thickness. The films absorb ultrabroad low‐frequency electromagnetic waves covering S, C, X, and Ku bands and achieve exceptional efficiency of 99.999% with a thickness of only 2.5 mm and a loading content of only 20%. This result originates from a synergistic effect of conductivity, heteroatoms, and pores and outperforms the state‐of‐the‐art polymers, carbons, and metals. This approach opens a way to electromagnetic wave absorption.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Covalent Organic Framework Applications · Perovskite Materials and Applications · 2D Materials and Applications

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

Affiliations

Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources Hainan University No 58, Renmin Avenue Haikou 570228 China

Department of Chemistry Faculty of Science National University of Singapore 3 Science Drive 3 Singapore 117543 Singapore

Funding

National Natural Science Foundation of China

References (23)

Show source-provided references
1. C. S.Baird AccessScience. McGraw‐Hill Education https://doi.org/10.1036/1097-8542.001600.10.1036/1097-8542.001600 ↗
2. 10.1021/acsnano.0c0998210.1021/acsnano.0c09982 ↗
3. 10.1002/advs.20210555310.1002/advs.202105553 ↗
4. 10.1080/15583724.2020.187049010.1080/15583724.2020.1870490 ↗
5. 10.1016/j.carbon.2020.10.06210.1016/j.carbon.2020.10.062 ↗
6. 10.1002/adfm.20220316110.1002/adfm.202203161 ↗
7. 10.1016/j.cej.2021.13311210.1016/j.cej.2021.133112 ↗
8. 10.1016/j.cej.2022.13657410.1016/j.cej.2022.136574 ↗
9. 10.1021/acs.chemrev.9b0055010.1021/acs.chemrev.9b00550 ↗
10. 10.1039/C9CS00890J10.1039/C9CS00890J ↗
11. Deng L. · Acc. Mater. Res. · 2022 · 2 · 327
12. 10.1002/anie.20211773810.1002/anie.202117738 ↗
13. 10.1038/s41467-022-29816-110.1038/s41467-022-29816-1 ↗
14. 10.1002/anie.20211502010.1002/anie.202115020 ↗
15. 10.1016/j.chempr.2021.08.01510.1016/j.chempr.2021.08.015 ↗
16. 10.1021/ja206846p10.1021/ja206846p ↗
17. 10.31635/ccschem.020.20200049110.31635/ccschem.020.202000491 ↗
18. 10.1021/acscentsci.0c0046310.1021/acscentsci.0c00463 ↗
19. 10.1002/adfm.20210050510.1002/adfm.202100505 ↗
20. 10.1007/s40820-021-00601-x10.1007/s40820-021-00601-x ↗
21. 10.1016/j.carbon.2020.07.02810.1016/j.carbon.2020.07.028 ↗
22. 10.1016/j.carbon.2021.08.02110.1016/j.carbon.2021.08.021 ↗
23. 10.1039/C7NR02628E10.1039/C7NR02628E ↗