Mechanical Toughening of Two-Dimensional Covalent Organic Frameworks Enabled by Graphene-Based Sandwich-Structured Nanocomposites
Source abstract
Abstract
Low resistance to fracture in two-dimensional covalent organic frameworks (2D COFs) limits their practical applications, especially in mechanically demanding fields, such as flexible electronics and sensing devices. We address this critical limitation by fabricating a sandwich-structured nanocomposite consisting of graphene layers sandwiched between 2D COF layers (2D COFs/graphene/2D COFs) via chemical vapor deposition. Our sandwich-structured nanocomposites exhibit a remarkable improvement in modulus E, fracture toughness K IC, and critical energy release rate G C compared to pure 2D COFs. This enhancement is likely due to the graphene layers as the backbone of the sandwich structure effectively carrying and redistributing mechanical stress within the nanocomposite. Our findings demonstrate that a sandwich structure can improve the mechanical robustness of a 2D COF so that it can preserve the functionality and mechanical integrity for applications in stretchable electronics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Covalent Organic Framework Applications · Graphene research and applications · Advanced Sensor and Energy Harvesting Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and NanoEngineering
Rice University
Department of Materials Science and Engineering
Cornell University
National Synchrotron Light Source II
Brookhaven National Laboratory
Rice Advanced Materials Institute
Department of Chemistry
Funding
Welch Foundation · Basic Energy Sciences · Division of Engineering Education and Centers · Division of Civil, Mechanical and Manufacturing Innovation
References (37)
Show source-provided references
1. 10.1021/acs.chemrev.8b0005610.1021/acs.chemrev.8b00056 ↗
2. 10.1038/s43586-022-00181-z10.1038/s43586-022-00181-z ↗
3. 10.1002/adma.20210494610.1002/adma.202104946 ↗
4. 10.1021/acs.accounts.4c0035610.1021/acs.accounts.4c00356 ↗
5. 10.1016/j.ccr.2021.21415210.1016/j.ccr.2021.214152 ↗
6. 10.1038/s43246-025-00801-710.1038/s43246-025-00801-7 ↗
7. 10.1002/adfm.20210050510.1002/adfm.202100505 ↗
8. 10.1021/acs.accounts.4c0049110.1021/acs.accounts.4c00491 ↗
9. 10.1021/acssensors.3c0026910.1021/acssensors.3c00269 ↗
10. 10.1016/j.matt.2021.01.00110.1016/j.matt.2021.01.001 ↗
11. 10.1016/j.matt.2021.02.00810.1016/j.matt.2021.02.008 ↗
12. 10.1021/acs.chemmater.1c0089510.1021/acs.chemmater.1c00895 ↗
13. 10.1126/sciadv.abb597610.1126/sciadv.abb5976 ↗
14. 10.1021/acsnano.3c1178710.1021/acsnano.3c11787 ↗
15. 10.1039/D2SC03489A10.1039/D2SC03489A ↗
16. 10.1021/acs.nanolett.2c0474710.1021/acs.nanolett.2c04747 ↗
17. 10.1038/s41467-024-53935-610.1038/s41467-024-53935-6 ↗
18. 10.1073/pnas.220867612010.1073/pnas.2208676120 ↗
19. 10.1038/s41586-024-07505-x10.1038/s41586-024-07505-x ↗
20. 10.1038/s44160-025-00791-x10.1038/s44160-025-00791-x ↗
21. 10.1039/D0TA05894G10.1039/D0TA05894G ↗
22. 10.1177/172988142092132710.1177/1729881420921327 ↗
23. 10.1016/j.matpr.2019.05.16910.1016/j.matpr.2019.05.169 ↗
24. 10.1021/acs.inorgchem.0c0042210.1021/acs.inorgchem.0c00422 ↗
25. 10.1021/prechem.3c0011810.1021/prechem.3c00118 ↗
26. 10.1021/acsmaterialslett.1c0078510.1021/acsmaterialslett.1c00785 ↗
27. 10.1039/D4TA01917B10.1039/D4TA01917B ↗
28. 10.1021/acsmaterialslett.2c0067210.1021/acsmaterialslett.2c00672 ↗
29. 10.1002/adma.20190577610.1002/adma.201905776 ↗
30. 10.1021/acsnano.2c1277310.1021/acsnano.2c12773 ↗
31. 10.1016/j.memsci.2022.12054410.1016/j.memsci.2022.120544 ↗
32. 10.1080/00018732.2011.58225110.1080/00018732.2011.582251 ↗
33. 10.1021/acsaem.2c0380610.1021/acsaem.2c03806 ↗
34. 10.1038/ncomms478210.1038/ncomms4782 ↗
35. 10.1039/C7NR04443G10.1039/C7NR04443G ↗
36. 10.1038/srep0270010.1038/srep02700 ↗
37. Meyers M. A. · 200810.1017/CBO9780511810947 ↗