Water‐Enabled Healing of Conducting Polymer Films
Source abstract
Abstract
Abstract The conducting polymer polyethylenedioxythiophene doped with polystyrene sulfonate (PEDOT:PSS) has become one of the most successful organic conductive materials due to its high air stability, high electrical conductivity, and biocompatibility. In recent years, a great deal of attention has been paid to its fundamental physicochemical properties, but its healability has not been explored in depth. This communication reports the first observation of mechanical and electrical healability of PEDOT:PSS thin films. Upon reaching a certain thickness (about 1 µm), PEDOT:PSS thin films damaged with a sharp blade can be electrically healed by simply wetting the damaged area with water. The process is rapid, with a response time on the order of 150 ms. Significantly, after being wetted the films are transformed into autonomic self‐healing materials without the need of external stimulation. This work reveals a new property of PEDOT:PSS and enables its immediate use in flexible and biocompatible electronics, such as electronic skin and bioimplanted electronics, placing conducting polymers on the front line for healing applications in electronics.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Conducting polymers and applications · Polymer composites and self-healing
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering Polytechnique Montréal Montréal Québec H3C3J7 Canada
Funding
Fonds de Recherche du Québec - Nature et Technologies · Natural Sciences and Engineering Research Council of Canada
References (25)
Show source-provided references
1. 10.1002/adma.20100303610.1002/adma.201003036 ↗
2. 10.1016/j.progpolymsci.2013.08.00110.1016/j.progpolymsci.2013.08.001 ↗
3. 10.1002/adma.20130224010.1002/adma.201302240 ↗
4. 10.1038/nnano.2012.19210.1038/nnano.2012.192 ↗
5. 10.1038/nature2010210.1038/nature20102 ↗
6. 10.1002/adma.20120130610.1002/adma.201201306 ↗
7. 10.1002/adma.20110288810.1002/adma.201102888 ↗
8. 10.1021/acs.nanolett.5b0306910.1021/acs.nanolett.5b03069 ↗
9. Shirakawa H. · J. Chem. Soc., Chem. Commun. · 1977 · 578
10. 10.1002/masy.1995100012810.1002/masy.19951000128 ↗
11. 10.1002/(SICI)1521-4095(200004)12:7<481::AID-ADMA481>3.0.CO;2-C10.1002/(SICI)1521-4095(200004)12:7<481::AID-ADMA481>3.0.CO;2-C ↗
12. 10.1002/adma.20150294710.1002/adma.201502947 ↗
13. 10.1016/j.progpolymsci.2008.08.00110.1016/j.progpolymsci.2008.08.001 ↗
14. J.Petajajarvi K.Mikhaylov A.Roivainen T.Hanninen M.Pettissalo presented at2015 14th Int. Conf. ITS Telecommunications (ITST) Copenhagen Denmark December2015.
15. 10.1063/1.490515410.1063/1.4905154 ↗
16. 10.1038/ncomms257310.1038/ncomms2573 ↗
17. 10.1126/science.120615710.1126/science.1206157 ↗
18. 10.1021/cm402200310.1021/cm4022003 ↗
19. 10.1002/adfm.20110177510.1002/adfm.201101775 ↗
20. 10.1016/j.orgel.2008.05.00610.1016/j.orgel.2008.05.006 ↗
21. 10.1002/adfm.20130217410.1002/adfm.201302174 ↗
22. 10.1021/acsami.5b0875310.1021/acsami.5b08753 ↗
23. 10.1021/acs.chemmater.7b0018110.1021/acs.chemmater.7b00181 ↗
24. 10.1039/C5TC03664J10.1039/C5TC03664J ↗
25. 10.1039/b615954k10.1039/b615954k ↗