Mussel-Inspired Adhesive and Carbon Fiber Conductive Hydrogel for Flexible Sensors
Source abstract
Abstract
Conductive hydrogels, which are considered to be a promising material for human motion detection sensors, often display low flexibility, limited elongation, and non-adhesive properties. Herein, a multifunctional hydrogel with self-adhesive, highly stretchable, and conductive properties was developed by introducing polydopamine (DA) and carbon fiber (CF) into polyacrylamide (PAAm) hydrogel. The DA was polymerized with oxygen to form polydopamine (PDA), and the PDA-CF-PAAm hydrogel was hybrid-crosslinked with covalent bonds and recoverable non-covalent bonds including hydrogen bonds and π-π stacking. Therefore, the prepared PDA-CF-PAAm hydrogel exhibits high and reversible stretchability. Additionally, the hydrogel demonstrates high adhesiveness on various substrate surfaces, such as paper, glass, rubber, and biological tissue surfaces due to the catechol groups of PDA. Furthermore, the obtained PDA-CF-PAAm hydrogel is conductive because of the addition of CF. As a result, the self-adhesive, highly stretchable, and conductive PDA-CF-PAAm hydrogel can be directly adhered to the skin as a strain sensor to monitor human body motion. This work may expand the scope of multifunctional hydrogel preparation for flexible wearable devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Conducting polymers and applications · Electrospun Nanofibers in Biomedical Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Low-Dimensional Materials Genome Initiative, College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, Guangdong 518060, P. R. China
Funding
Guangdong Province Introduction of Innovative R&D Team · Special Project for Research and Development in Key areas of Guangdong Province · National Natural Science Foundation of China
References (37)
Show source-provided references
1. 10.1039/D2TC01096H10.1039/D2TC01096H ↗
2. 10.1039/D2MH00456A10.1039/D2MH00456A ↗
3. 10.1002/smll.20210151810.1002/smll.202101518 ↗
4. 10.1021/acsapm.2c0066810.1021/acsapm.2c00668 ↗
5. 10.1016/j.cej.2020.12763710.1016/j.cej.2020.127637 ↗
6. 10.1016/j.cej.2019.12191510.1016/j.cej.2019.121915 ↗
7. 10.1039/C9TC04006D10.1039/C9TC04006D ↗
8. 10.1016/j.ijbiomac.2022.09.18110.1016/j.ijbiomac.2022.09.181 ↗
9. 10.1039/C9CS00849G10.1039/C9CS00849G ↗
10. 10.1002/adfm.20190995410.1002/adfm.201909954 ↗
11. 10.1038/s41467-019-09351-210.1038/s41467-019-09351-2 ↗
12. 10.1002/adfm.20190767810.1002/adfm.201907678 ↗
13. 10.1002/adfm.20201046110.1002/adfm.202010461 ↗
14. 10.1016/j.eurpolymj.2023.11203410.1016/j.eurpolymj.2023.112034 ↗
15. 10.1016/j.apsusc.2016.02.13510.1016/j.apsusc.2016.02.135 ↗
16. 10.1039/C4TB02067G10.1039/C4TB02067G ↗
17. 10.1002/adfm.20170419510.1002/adfm.201704195 ↗
18. 10.1016/j.carbon.2017.09.07110.1016/j.carbon.2017.09.071 ↗
19. 10.1002/adma.20210990410.1002/adma.202109904 ↗
20. 10.1016/j.cej.2021.13251510.1016/j.cej.2021.132515 ↗
21. 10.1016/j.nanoen.2022.10737410.1016/j.nanoen.2022.107374 ↗
22. 10.1021/acsapm.2c0148810.1021/acsapm.2c01488 ↗
23. 10.1039/C9TB01039D10.1039/C9TB01039D ↗
24. 10.1039/D0SM01234C10.1039/D0SM01234C ↗
25. 10.1002/admt.20220176710.1002/admt.202201767 ↗
26. 10.1039/D1TC05864A10.1039/D1TC05864A ↗
27. 10.3390/ma204236910.3390/ma2042369 ↗
28. 10.1016/j.compositesa.2016.10.01810.1016/j.compositesa.2016.10.018 ↗
29. 10.1002/adfm.20210243310.1002/adfm.202102433 ↗
30. 10.1038/am.2017.3310.1038/am.2017.33 ↗
31. 10.1002/adma.20140370910.1002/adma.201403709 ↗
32. 10.1021/la400587j10.1021/la400587j ↗
33. 10.1016/j.apsusc.2018.03.05710.1016/j.apsusc.2018.03.057 ↗
34. 10.1016/j.compositesb.2022.10963910.1016/j.compositesb.2022.109639 ↗
35. 10.1039/C7MH00917H10.1039/C7MH00917H ↗
36. 10.1039/D2CS00618A10.1039/D2CS00618A ↗
37. 10.1002/marc.20220007510.1002/marc.202200075 ↗