High Electron Mobility in Conjugated Polymers Processed with Nonchlorinated Solvents for Organic Thin Film Transistors
Source abstract
Abstract
Herein, we report a series of conjugated polymers P1 – P4, which were synthesized through aldol polymerization using toluene as the solvent and p -toluene sulfonic acid as the sole catalyst. We investigated their solubility, optical and electrochemical properties, wettability, and aggregation behaviors in (or treated with) 2-methyltetrahydrofuran (2-MeTHF) and o -dichlorobenzene ( o -DCB). We found that the 2-MeTHF-treated thin films of P1 – P4 have slightly different frontier molecular orbital energy levels in comparison with those of their o -DCB-treated counterparts, respectively. Moreover, 2-MeTHF-processed organic thin film transistors (OTFTs) based on these polymers exhibited a higher n-type transport performance. Notably, the P2 -based device afforded the maximum electron mobility of 3.14 cm 2 V –1 s –1, which is among the highest for the n-type polymer-based OTFTs processed with nonchlorinated solvents to date. Microstructure characterizations further revealed that all these 2-MeTHF-treated thin films have enhanced film morphology and molecular orientation stacking compared to those of their respective o -DCB-treated ones.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Organic Light-Emitting Diodes Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing National Laboratory for Molecular Sciences, CAS Research/Education Center for Excellence in Molecular Sciences
Institute of Chemistry, Chinese Academy of Sciences
School of Chemical Sciences
University of Chinese Academy of Sciences
School of Materials Science and Engineering
University of Science and Technology Beijing
Funding
Beijing National Laboratory for Molecular Sciences · National Key Research and Development Program of China · National Natural Science Foundation of China · Chinese Academy of Sciences
References (57)
Show source-provided references
1. 10.1021/cr100380z10.1021/cr100380z ↗
2. 10.1021/ja400881n10.1021/ja400881n ↗
3. 10.1002/anie.20230355110.1002/anie.202303551 ↗
4. 10.1038/s41467-024-55494-210.1038/s41467-024-55494-2 ↗
5. 10.1038/s41586-024-07724-210.1038/s41586-024-07724-2 ↗
6. 10.1038/s41467-023-43505-710.1038/s41467-023-43505-7 ↗
7. 10.1002/anie.20231938010.1002/anie.202319380 ↗
8. 10.1002/adma.20230024010.1002/adma.202300240 ↗
9. 10.1038/nature2010210.1038/nature20102 ↗
10. 10.1038/nature2549410.1038/nature25494 ↗
11. 10.1126/science.ade008610.1126/science.ade0086 ↗
12. 10.1021/acs.chemmater.9b0442510.1021/acs.chemmater.9b04425 ↗
13. 10.1002/adma.20230014510.1002/adma.202300145 ↗
14. 10.1002/adma.20200612010.1002/adma.202006120 ↗
15. 10.1002/adma.20190388210.1002/adma.201903882 ↗
16. 10.1039/D2SC06702A10.1039/D2SC06702A ↗
17. 10.1038/s41467-021-27832-110.1038/s41467-021-27832-1 ↗
18. 10.1002/anie.20230992210.1002/anie.202309922 ↗
19. 10.1021/jacs.3c1445010.1021/jacs.3c14450 ↗
20. 10.1021/ja505574a10.1021/ja505574a ↗
21. 10.1021/ma401190r10.1021/ma401190r ↗
22. 10.1002/adma.20150289610.1002/adma.201502896 ↗
23. 10.1038/s41557-018-0200-y10.1038/s41557-018-0200-y ↗
24. 10.1016/j.matt.2022.04.00810.1016/j.matt.2022.04.008 ↗
25. 10.1038/s41467-018-02852-610.1038/s41467-018-02852-6 ↗
26. 10.1021/jacs.0c1036510.1021/jacs.0c10365 ↗
27. 10.1021/jacs.2c0073510.1021/jacs.2c00735 ↗
28. 10.31635/ccschem.023.20220245810.31635/ccschem.023.202202458 ↗
29. 10.1002/ange.20231187910.1002/ange.202311879 ↗
30. 10.1002/adma.20170528610.1002/adma.201705286 ↗
31. 10.1002/anie.20230186310.1002/anie.202301863 ↗
32. 10.1002/anie.20210739510.1002/anie.202107395 ↗
33. 10.1002/anie.20201521610.1002/anie.202015216 ↗
34. 10.1002/adma.20150033510.1002/adma.201500335 ↗
35. 10.1002/advs.20190241210.1002/advs.201902412 ↗
36. 10.1126/sciadv.adf349510.1126/sciadv.adf3495 ↗
37. 10.1039/b617536h10.1039/b617536h ↗
38. 10.1039/D1GC03662A10.1039/D1GC03662A ↗
39. 10.1038/s41586-022-05295-810.1038/s41586-022-05295-8 ↗
40. 10.1146/annurev-physchem-040513-10363910.1146/annurev-physchem-040513-103639 ↗
41. 10.1038/nmat464510.1038/nmat4645 ↗
42. 10.1002/adma.20170546310.1002/adma.201705463 ↗
43. 10.1002/adma.20160266010.1002/adma.201602660 ↗
44. 10.1002/anie.20200758910.1002/anie.202007589 ↗
45. 10.1038/s41563-020-0647-210.1038/s41563-020-0647-2 ↗
46. 10.1002/adma.20220305510.1002/adma.202203055 ↗
47. 10.1016/j.polymer.2020.12250110.1016/j.polymer.2020.122501 ↗
48. 10.1038/s41467-019-13155-910.1038/s41467-019-13155-9 ↗
49. 10.1016/j.synthmet.2014.12.00910.1016/j.synthmet.2014.12.009 ↗
50. 10.1016/j.spmi.2015.03.04510.1016/j.spmi.2015.03.045 ↗
51. 10.1021/acsami.7b0807110.1021/acsami.7b08071 ↗
52. 10.1093/nsr/nwab14510.1093/nsr/nwab145 ↗
53. 10.1021/acs.chemmater.5b0017310.1021/acs.chemmater.5b00173 ↗
54. 10.1002/advs.20200201010.1002/advs.202002010 ↗
55. 10.1039/D3CC00191A10.1039/D3CC00191A ↗
56. 10.1039/C7TC04823H10.1039/C7TC04823H ↗
57. 10.1039/C7EE01943B10.1039/C7EE01943B ↗