A Stretchable Polymer Conductor Through the Mutual Plasticization Effect
Source abstract
Abstract
Abstract Intrinsically stretchable conductors play key roles in the dynamic interfacing of electronic devices with soft human tissues. However, it is difficult to simultaneously achieve high electrical conductivity and mechanical stretchability. Here, highly stretchable and conductive thin film electrodes are prepared by combining PEDOT:PSS and a mutually plasticized polymer dopant. Notably, harsh acid treatment for conductivity enhancement is avoided, and good solvent tolerance and high optical transparency are realized, all of which are essential to device fabrication. A transparent electrochromic display is further developed that can bear stretching up to 80% strain, demonstrating its promising application in next‐generation optoelectronics.
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Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Conducting polymers and applications · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Tianjin Key Laboratory of Molecular Optoelectronic Sciences Department of Chemistry School of Science Tianjin University and Collaborative Innovation Center of Chemical Science and Engineering Tianjin 300072 P. R. China
Haihe Laboratory of Sustainable Chemical Transformations Tianjin 300192 P. R. China
Funding
National Key Research and Development Program of China · National Natural Science Foundation of China
References (45)
Show source-provided references
1. 10.1126/science.abo663110.1126/science.abo6631 ↗
2. 10.1126/science.abn514210.1126/science.abn5142 ↗
3. 10.1038/nnano.2012.19210.1038/nnano.2012.192 ↗
4. 10.1002/smm2.105910.1002/smm2.1059 ↗
5. 10.1038/s41928-020-0422-z10.1038/s41928-020-0422-z ↗
6. 10.1002/adfm.20180368410.1002/adfm.201803684 ↗
7. 10.1038/s41565-018-0226-810.1038/s41565-018-0226-8 ↗
8. 10.1038/nature2100410.1038/nature21004 ↗
9. 10.1002/adma.20170280010.1002/adma.201702800 ↗
10. 10.1002/adfm.20130390510.1002/adfm.201303905 ↗
11. 10.1002/aelm.20150001710.1002/aelm.201500017 ↗
12. 10.1126/sciadv.160207610.1126/sciadv.1602076 ↗
13. 10.1021/acs.macromol.0c0230910.1021/acs.macromol.0c02309 ↗
14. 10.1021/acsami.9b0732510.1021/acsami.9b07325 ↗
15. 10.1021/accountsmr.0c0002110.1021/accountsmr.0c00021 ↗
16. 10.1126/science.aah449610.1126/science.aah4496 ↗
17. 10.1021/acsami.5b0449210.1021/acsami.5b04492 ↗
18. 10.1002/adma.20110479510.1002/adma.201104795 ↗
19. Hao H. · Sci Adv · 2022 · 8 · 47
20. 10.1126/science.abj756410.1126/science.abj7564 ↗
21. 10.1016/j.chempr.2021.06.00410.1016/j.chempr.2021.06.004 ↗
22. 10.1126/science.aaz669410.1126/science.aaz6694 ↗
23. 10.1038/s41586-022-04400-110.1038/s41586-022-04400-1 ↗
24. 10.1002/adma.20150007810.1002/adma.201500078 ↗
25. 10.1002/adma.20130461110.1002/adma.201304611 ↗
26. 10.1021/jacs.9b0606310.1021/jacs.9b06063 ↗
27. 10.1016/j.msec.2010.11.00410.1016/j.msec.2010.11.004 ↗
28. 10.1149/05811.0049ecst10.1149/05811.0049ecst ↗
29. 10.1038/s41467-018-05222-410.1038/s41467-018-05222-4 ↗
30. 10.1038/s41551-018-0335-610.1038/s41551-018-0335-6 ↗
31. 10.1002/adfm.20100229010.1002/adfm.201002290 ↗
32. 10.1021/ma990567410.1021/ma9905674 ↗
33. 10.1002/aenm.20160211610.1002/aenm.201602116 ↗
34. 10.1002/adfm.20040001610.1002/adfm.200400016 ↗
35. 10.1021/ma900327d10.1021/ma900327d ↗
36. 10.1002/polb.1065910.1002/polb.10659 ↗
37. 10.1021/acsami.6b0031710.1021/acsami.6b00317 ↗
38. 10.1039/C1EE02475B10.1039/C1EE02475B ↗
39. 10.1038/s41467-018-06084-610.1038/s41467-018-06084-6 ↗
40. 10.1021/ja806389b10.1021/ja806389b ↗
41. 10.1038/s41467-018-06084-610.1038/s41467-018-06084-6 ↗
42. 10.1038/s41586-021-04053-610.1038/s41586-021-04053-6 ↗
43. 10.1016/j.orgel.2011.12.00710.1016/j.orgel.2011.12.007 ↗
44. 10.1038/s41928-022-00843-610.1038/s41928-022-00843-6 ↗
45. 10.1039/C5CC07122D10.1039/C5CC07122D ↗