Super Tough, Ultrastretchable Hydrogel with Multistimuli Responsiveness
Source abstract
Abstract
The research of hydrogels has been increasingly focused on designing an effective energy dissipation structure in recent years. Here, we report a kind of novel supramolecular cross-linker, which was formed by self-assembling amphiphilic block copolymers with guest groups at the end and vinyl-functionalized cyclodextrin (CD) through host-guest interaction. These cross-linkers could dissipate energy effectively since they combined multiple sacrificial mechanisms across multiscales through physical interactions. The resulted hydrogel shows distinguishing mechanical properties (fracture toughness of 2.68 ± 0.69 MJ/m3, tension strength of up to 475 kPa, uniaxial stretch over 2100%), remarkable fatigue resistance, and thermal- and light-responsive behaviors.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Hydrogels: synthesis, properties, applications · Advanced Polymer Synthesis and Characterization · Advanced Materials and Mechanics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Polymer Materials Engineering (Sichuan University), Polymer Research Institute of Sichuan University, Chengdu 610065, China
Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, China
Funding
National Natural Science Foundation of China · State Key Laboratory of Polymer Materials Engineering, Sichuan University
References (34)
Show source-provided references
1. 10.1039/C4TB00775A10.1039/C4TB00775A ↗
2. 10.1016/j.biomaterials.2014.03.00110.1016/j.biomaterials.2014.03.001 ↗
3. 10.1021/cr200157d10.1021/cr200157d ↗
4. 10.1021/nl401088b10.1021/nl401088b ↗
5. 10.1002/adma.20170032110.1002/adma.201700321 ↗
6. 10.1016/j.ijpharm.2016.05.01310.1016/j.ijpharm.2016.05.013 ↗
7. 10.1039/C4CC04760E10.1039/C4CC04760E ↗
8. 10.1002/adma.20130081710.1002/adma.201300817 ↗
9. 10.1002/marc.20060015910.1002/marc.200600159 ↗
10. 10.1002/adma.20060253310.1002/adma.200602533 ↗
11. 10.1002/pi.235210.1002/pi.2352 ↗
12. 10.1021/bm400564510.1021/bm4005645 ↗
13. 10.1021/acsami.7b0016910.1021/acsami.7b00169 ↗
14. 10.1039/C6SC02354A10.1039/C6SC02354A ↗
15. 10.1039/C3SM52272E10.1039/C3SM52272E ↗
16. 10.1016/j.biomaterials.2014.10.03210.1016/j.biomaterials.2014.10.032 ↗
17. 10.1039/C7SM00045F10.1039/C7SM00045F ↗
18. 10.1002/adma.20060253310.1002/adma.200602533 ↗
19. 10.1021/acs.macromol.7b0048310.1021/acs.macromol.7b00483 ↗
20. 10.1038/ncomms322610.1038/ncomms3226 ↗
21. 10.1002/adfm.20140435710.1002/adfm.201404357 ↗
22. 10.1021/mz500221j10.1021/mz500221j ↗
23. 10.1039/C4CC10094H10.1039/C4CC10094H ↗
24. 10.1039/c2sm25084e10.1039/c2sm25084e ↗
25. 10.1002/anie.20150579010.1002/anie.201505790 ↗
26. 10.1002/pola.2377110.1002/pola.23771 ↗
27. 10.1039/C4CC03131H10.1039/C4CC03131H ↗
28. 10.1021/acsami.6b1464010.1021/acsami.6b14640 ↗
29. 10.1021/ja971052010.1021/ja9710520 ↗
30. 10.1021/acs.macromol.6b0144810.1021/acs.macromol.6b01448 ↗
31. 10.1038/s41467-017-02198-510.1038/s41467-017-02198-5 ↗
32. 10.1002/anie.20140740210.1002/anie.201407402 ↗
33. 10.1039/c0cs00153h10.1039/c0cs00153h ↗
34. 10.1039/C6CC03587F10.1039/C6CC03587F ↗