Thiadizoloquinoxaline-Based Low-Bandgap Conjugated Polymers as Ambipolar Semiconductors for Organic Field Effect Transistors
Source abstract
Abstract
Two novel conjugated polymers with high molecular weight, PBDTTQ-3 and PAPhTQ, were synthesized by tuning alkyl chains and alternating the electron-donating ability of the thiadiazoloquinoxaline (TQ) moiety. Both polymers have excellent solubility in common organic solvents. UV–vis–NIR absorption and cyclic voltammetry indicate a bandgap of (0.76 eV) and high electron affinity level (−4.08 eV) for PBDTTQ-3 . Two dimensional wide-angle X-ray scattering shows that both polymers are only poorly ordered in the bulk but possess a close π-stacking distance of 0.36 nm. Despite the disorder in thin film observed by grazing incidence wide-angle X-ray scattering, PBDTTQ-3 exhibits good ambipolar transport, with a maximum hole mobility of 0.22 cm 2 V –1 s –1 and comparable electron mobility of 0.21 cm 2 V –1 s –1 .
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany
Funding
European Research Council · Deutsche Forschungsgemeinschaft · China Scholarship Council
References (49)
Show source-provided references
1. Kelley T. W. · Chem. Mater. · 2004 · 16 · 441310.1021/cm049614j ↗
2. Forrest S. R. · Nature · 2004 · 428 · 91110.1038/nature02498 ↗
3. Tsao H. N. · J. Am. Chem. Soc. · 2011 · 133 · 260510.1021/ja108861q ↗
4. Capelli R. · Nat. Mater. · 2010 · 9 · 49610.1038/nmat2751 ↗
5. Chua L.-L. · Nature · 2005 · 434 · 19410.1038/nature03376 ↗
6. Steckler T. T. · J. Am. Chem. Soc. · 2009 · 131 · 282410.1021/ja809372u ↗
7. Fan J. · Adv. Mater. · 2012 · 24 · 218610.1002/adma.201103836 ↗
8. Yuen J. D. · J. Am. Chem. Soc. · 2011 · 133 · 2079910.1021/ja205566w ↗
9. Chen H. · Chem. Mater. · 2013 · 25 · 358910.1021/cm401130n ↗
10. Chen Z. Y. · Adv. Mater. · 2012 · 24 · 64710.1002/adma.201102786 ↗
11. Sonar P. · Chem. Commun. · 2012 · 48 · 838310.1039/c2cc33093h ↗
12. Lee J. · J. Am. Chem. Soc. · 2013 · 135 · 954010.1021/ja403949g ↗
13. Lei T. · J. Am. Chem. Soc. · 2012 · 134 · 2002510.1021/ja310283f ↗
14. Lei T. · Adv. Mater. · 2013 · 25 · 658910.1002/adma.201302278 ↗
15. Kitamura C. · Chem. Mater. · 1996 · 8 · 57010.1021/cm950467m ↗
16. Inganäs O. · Acc. Chem. Res. · 2009 · 42 · 173110.1021/ar900073s ↗
17. Chen M. X. · Synth. Met. · 2004 · 146 · 23310.1016/j.synthmet.2004.08.002 ↗
18. Admassie S. · Synth. Met. · 2006 · 156 · 61410.1016/j.synthmet.2006.02.013 ↗
19. Cheng K.-F. · J. Polym. Sci., Part A: Polym. Chem. · 2008 · 46 · 630510.1002/pola.22942 ↗
20. Sun M. · J. Polym. Sci., Part A: Polym. Chem. · 2008 · 46 · 300710.1002/pola.22638 ↗
21. Yi H. · Macromol. Rapid Commun. · 2008 · 29 · 180410.1002/marc.200800440 ↗
22. Yu C.-Y. · Chem. Mater. · 2009 · 21 · 326210.1021/cm9007798 ↗
23. Zoombelt A. P. · Org. Lett. · 2009 · 11 · 90310.1021/ol802839z ↗
24. Cai T. · Sol. Energy Mater. Sol. Cells · 2010 · 94 · 127510.1016/j.solmat.2010.03.024 ↗
25. Inganäs O. · Adv. Mater. · 2010 · 22 · E10010.1002/adma.200904407 ↗
26. Zhang X. · J. Mater. Chem. · 2010 · 20 · 12310.1039/B915940A ↗
27. Dallos T. · J. Am. Chem. Soc. · 2011 · 133 · 1389810.1021/ja2057709 ↗
28. Dexter Tam T. L. · J. Mater. Chem. · 2012 · 22 · 1852810.1039/c2jm33317a ↗
29. Lee Y. · J. Phys. Chem. C · 2012 · 116 · 837910.1021/jp2124247 ↗
30. Keshtov M. L. · Polym. Chem. · 2013 · 4 · 403310.1039/c3py00391d ↗
31. Steckler T. T. · Macromol. Rapid Commun. · 2013 · 34 · 99010.1002/marc.201300240 ↗
32. Steckler T. T. · J. Am. Chem. Soc. · 2014 · 136 · 119010.1021/ja410527n ↗
33. An C. · Macromolecules · 2014 · 47 · 97910.1021/ma401938m ↗
34. Beaujuge P. M. · J. Am. Chem. Soc. · 2012 · 134 · 894410.1021/ja301898h ↗
35. Chen H. · Adv. Mater. · 2012 · 24 · 461810.1002/adma.201201318 ↗
36. Osaka I. · J. Am. Chem. Soc. · 2012 · 134 · 349810.1021/ja210687r ↗
37. Pisula W. · J. Am. Chem. Soc. · 2004 · 126 · 807410.1021/ja048351r ↗
38. Arroyave F. A. · Org. Lett. · 2012 · 14 · 613810.1021/ol302704v ↗
39. Goto H. · Angew. Chem., Int. Ed. · 2005 · 44 · 432210.1002/anie.200462859 ↗
40. Guo X. · Adv. Mater. · 2013 · 25 · 546710.1002/adma.201302052 ↗
41. Bredas J.-L. · Mater. Horiz. · 2014 · 1 · 1710.1039/C3MH00098B ↗
42. Sariciftci N. S. · 1997
43. Braga D. · Adv. Mater. · 2009 · 21 · 147310.1002/adma.200802733 ↗
44. Jones B. A. · J. Am. Chem. Soc. · 2007 · 129 · 1525910.1021/ja075242e ↗
45. Osaka I. · J. Am. Chem. Soc. · 2009 · 131 · 252110.1021/ja801475h ↗
46. Osaka I. · Chem. Mater. · 2010 · 22 · 419110.1021/cm101052b ↗
47. Yuen J. D. · Adv. Mater. · 2011 · 23 · 3875
48. Ko S. · J. Am. Chem. Soc. · 2011 · 133 · 1672210.1021/ja207429s ↗
49. Liu J. · Adv. Funct. Mater. · 2009 · 19 · 342710.1002/adfm.200900926 ↗