Enhancing the Solubility of Semiconducting Polymers in Eco-Friendly Solvents with Carbohydrate-Containing Side Chains
Source abstract
Abstract
Semiconducting polymers are at the forefront of next-generation organic electronics due to their robust mechanical and optoelectronic properties. However, their extended π-conjugation often leads to materials with low solubilities in common organic solvents, thus requiring processing in high-boiling-point and toxic halogenated solvents to generate thin-film devices. To address this environmental concern, a natural product-inspired side-chain engineering approach was used to incorporate galactose-containing moieties into semiconducting polymers toward improved processability in greener solvents. Novel isoindigo-based polymers with different ratios of galactose-containing side chains were synthesized to improve the solubilities of the organic semiconductors in alcohol-based solvents. The addition of carbohydrate-containing side chains to π-conjugated polymers was found to considerably impact the intermolecular aggregation of the materials and their microstructures in the solid state as confirmed by atomic force microscopy and grazing-incidence wide-angle X-ray scattering. The charge transport characteristics of the new semiconductors were evaluated by the fabrication of organic field-effect transistors prepared from both toxic halogenated and greener alcohol-based solvents. Importantly, the incorporation of carbohydrate-containing side chains was shown to have very little detrimental impact on the electronic properties of the polymer when processed from green solvents.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Synthesis and properties of polymers
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario N9B 3P4, Canada
School of Polymer Science and Engineering, The University of Southern Mississippi, Hattiesburg, Mississippi 39406, United States
Funding
Basic Energy Sciences · Canada Foundation for Innovation · University of Windsor · Office of Integrative Activities · Natural Sciences and Engineering Research Council of Canada · Ontario Ministry of Research, Innovation and Science
References (58)
Show source-provided references
1. 10.1016/j.future.2013.01.01010.1016/j.future.2013.01.010 ↗
2. 10.1039/C3TC31765J10.1039/C3TC31765J ↗
3. 10.3390/jsan103021710.3390/jsan1030217 ↗
4. 10.1088/0022-3727/45/10/10300110.1088/0022-3727/45/10/103001 ↗
5. 10.1038/s41467-017-02685-910.1038/s41467-017-02685-9 ↗
6. Zeng W. · Adv. Mater. · 2014 · 31 · 531010.1002/adma.201400633 ↗
7. 10.1002/adma.20130224010.1002/adma.201302240 ↗
8. 10.1039/C5TB00173K10.1039/C5TB00173K ↗
9. 10.1039/C5MH00164A10.1039/C5MH00164A ↗
10. 10.1002/aelm.20170042910.1002/aelm.201700429 ↗
11. 10.1021/cm501021v10.1021/cm501021v ↗
12. 10.1002/adfm.20200066310.1002/adfm.202000663 ↗
13. 10.1002/tcr.20180016310.1002/tcr.201800163 ↗
14. 10.1038/nature2010210.1038/nature20102 ↗
15. 10.1088/2058-8585/aa9c9b10.1088/2058-8585/aa9c9b ↗
16. 10.1021/acs.macromol.7b0086010.1021/acs.macromol.7b00860 ↗
17. 10.1039/C8PY01207E10.1039/C8PY01207E ↗
18. 10.1039/C4EE02657H10.1039/C4EE02657H ↗
19. 10.1002/adfm.20110090410.1002/adfm.201100904 ↗
20. 10.1021/ar300330510.1021/ar3003305 ↗
21. 10.1039/C4PY01222D10.1039/C4PY01222D ↗
22. 10.1039/D0TC04085A10.1039/D0TC04085A ↗
23. 10.1016/S0926-9614(96)80035-910.1016/S0926-9614(96)80035-9 ↗
24. 10.1021/acs.chemmater.6b0177610.1021/acs.chemmater.6b01776 ↗
25. 10.1021/cr200263w10.1021/cr200263w ↗
26. 10.1021/ja202877q10.1021/ja202877q ↗
27. 10.1021/am201290510.1021/am2012905 ↗
28. 10.1021/acscentsci.7b0023210.1021/acscentsci.7b00232 ↗
29. 10.1039/C9TC04808A10.1039/C9TC04808A ↗
30. 10.1021/acs.macromol.7b0045210.1021/acs.macromol.7b00452 ↗
31. 10.1021/acsapm.9b0004410.1021/acsapm.9b00044 ↗
32. 10.1002/aenm.20190266210.1002/aenm.201902662 ↗
33. 10.1021/ar400254j10.1021/ar400254j ↗
34. 10.1109/JSEN.2014.237520310.1109/JSEN.2014.2375203 ↗
35. Enlund N. · 2015 · 42
36. 10.1016/j.tetlet.2008.12.04310.1016/j.tetlet.2008.12.043 ↗
37. 10.1016/j.addr.2007.05.01310.1016/j.addr.2007.05.013 ↗
38. 10.1016/j.biomaterials.2012.02.03310.1016/j.biomaterials.2012.02.033 ↗
39. 10.1073/pnas.170147811410.1073/pnas.1701478114 ↗
40. 10.1002/iub.26210.1002/iub.262 ↗
41. 10.1002/adma.20120268910.1002/adma.201202689 ↗
42. 10.1039/C5TC02565F10.1039/C5TC02565F ↗
43. 10.1021/acs.macromol.7b0239310.1021/acs.macromol.7b02393 ↗
44. 10.1021/jacs.5b0973710.1021/jacs.5b09737 ↗
45. 10.1021/ma100307m10.1021/ma100307m ↗
46. 10.1002/adfm.20170197310.1002/adfm.201701973 ↗
47. 10.1021/acsami.8b2274610.1021/acsami.8b22746 ↗
48. 10.1039/c0gc00918k10.1039/c0gc00918k ↗
49. Kipphan H. · 200110.1007/978-3-540-29900-4 ↗
50. 10.1021/cm049611710.1021/cm0496117 ↗
51. 10.1039/c2tc00255h10.1039/c2tc00255h ↗
52. 10.1002/aelm.20180089910.1002/aelm.201800899 ↗
53. Diao Y. · Nat. Commun. · 2015 · 6 · 110.1038/ncomms8955 ↗
54. 10.1021/ja902995710.1021/ja9029957 ↗
55. 10.1021/acs.macromol.6b0054010.1021/acs.macromol.6b00540 ↗
56. 10.1021/acs.chemmater.8b0253510.1021/acs.chemmater.8b02535 ↗
57. 10.1021/om201217r10.1021/om201217r ↗
58. 10.1002/marc.20180009210.1002/marc.201800092 ↗