journal article·2018-08-08

Copolymers of Bis-Diketopyrrolopyrrole and Benzothiadiazole Derivatives for High-Performance Ambipolar Field-Effect Transistors on Flexible Substrates

Jinyang Chen, Yingying Jiang, Jie Yang, Yunlong Sun, Longxian Shi, Yang Ran, Qingsong Zhang, Yuanping Yi, Shuai Wang, Yunlong Guo, Yunqi Liu

ACS Applied Materials & Interfaces· Volume 10· Issue 31
Publisher page

Abstract

We develop an “acceptor dimerization” strategy by a bis-diketopyrrolopyrrole (2DPP) for an ambipolar organic semiconductor. Copolymers of 2DPP and benzothiadiazole (BTz) derivatives, P2DPP-BTz and P2DPP-2FBTz, are designed and synthesized. Both of the polymers exhibit narrow optical bandgaps of ca. 1.30 eV. The strong electron-withdrawing property of 2DPP results in low-lying lowest unoccupied molecular orbital (LUMO) energy levels of the polymers, improving the electron mobilities. 2D grazing incident X-ray diffraction and atomic force microscopy indicate that the P2DPP-BTz exhibits a small π–π stacking distance of 3.59 Å and a smooth interface, thus promoting high mobility. To take full advantage of the flexibility of organic semiconductors, flexible field-effect transistors (FETs) were fabricated on poly(ethylene terephthalate) (PET) substrates. The FETs based on P2DPP-BTz show high performance with hole and electron mobilities of 1.73 and 2.58 cm2 V–1 s–1, respectively. Our results demonstrate that the 2DPP acceptor is a promising building block for high-mobility ambipolar polymers.
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

Key Laboratory of Organic Solids, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China

University of Chinese Academy of Sciences, Beijing 100049, China

Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074, China

Funding

Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Chinese Academy of Sciences

References (41)

Show source-provided references
1. 10.1038/natur10.1038/natur ↗
2. 10.1021/cr900150b10.1021/cr900150b ↗
3. 10.1021/cr100380z10.1021/cr100380z ↗
4. 10.1002/adma.20130434610.1002/adma.201304346 ↗
5. 10.1021/cr500225d10.1021/cr500225d ↗
6. 10.1039/c2ee23505f10.1039/c2ee23505f ↗
7. 10.1002/adma.20150040110.1002/adma.201500401 ↗
8. 10.1021/ar400254j10.1021/ar400254j ↗
9. 10.1002/adma.20130494510.1002/adma.201304945 ↗
10. 10.1039/c0cc00078g10.1039/c0cc00078g ↗
11. 10.1002/anie.20130974610.1002/anie.201309746 ↗
12. 10.1021/ja205398u10.1021/ja205398u ↗
13. 10.1021/cm504545e10.1021/cm504545e ↗
14. 10.1002/adma.20160241010.1002/adma.201602410 ↗
15. 10.1021/ja403949g10.1021/ja403949g ↗
16. 10.1002/adma.20130598110.1002/adma.201305981 ↗
17. 10.1002/adma.20150289610.1002/adma.201502896 ↗
18. 10.1002/adma.20160616210.1002/adma.201606162 ↗
19. 10.1002/adma.20170211510.1002/adma.201702115 ↗
20. 10.1002/adma.20160621710.1002/adma.201606217 ↗
21. 10.1021/acs.chemmater.5b0001810.1021/acs.chemmater.5b00018 ↗
22. 10.1002/adma.20110113410.1002/adma.201101134 ↗
23. 10.1002/adma.20110278610.1002/adma.201102786 ↗
24. 10.1002/adfm.20100265110.1002/adfm.201002651 ↗
25. 10.1021/acsami.5b1205010.1021/acsami.5b12050 ↗
26. 10.1002/adfm.20160428610.1002/adfm.201604286 ↗
27. 10.1002/anie.20170842110.1002/anie.201708421 ↗
28. 10.1002/adma.20110452210.1002/adma.201104522 ↗
29. 10.1021/acs.chemmater.6b0367110.1021/acs.chemmater.6b03671 ↗
30. 10.1038/nmat106110.1038/nmat1061 ↗
31. 10.1038/nature2010210.1038/nature20102 ↗
32. 10.1126/science.aah449610.1126/science.aah4496 ↗
33. 10.1021/cm301910t10.1021/cm301910t ↗
34. 10.1021/ja412533d10.1021/ja412533d ↗
35. 10.1021/acs.chemmater.5b0334910.1021/acs.chemmater.5b03349 ↗
36. 10.1021/acs.chemmater.6b0015410.1021/acs.chemmater.6b00154 ↗
37. 10.1021/am505925w10.1021/am505925w ↗
38. 10.1021/jacs.5b1044510.1021/jacs.5b10445 ↗
39. 10.1021/ja108599610.1021/ja1085996 ↗
40. 10.1002/adma.20130428010.1002/adma.201304280 ↗
41. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, G. A.; Nakatsuji, H.; Caricato, M.; Li, X.; Hratchian, H. P.; Izmaylov, A. F.; Bloino, J.; Zheng, G.; Sonnenberg, J. L.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Montgomery, J. A., Jr.; Peralta, J. E.; Ogliaro, F.; Bearpark, M.; Heyd, J. J.; Brothers, E.; Kudin, K. N.; Staroverov, V. N.; Kobayashi, R.; Normand, J.; Raghavachari, K.; Rendell, A.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Rega, N.; Millam, J. M.; Klene, M.; Knox, J. E.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Martin, R. L.; Morokuma, K.; Zakrzewski, V. G.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Dapprich, S.; Daniels, A. D.; Farkas, O.; Foresman, J. B.; Ortiz, J. V.; Cioslowski, J.; Fox, D. J. Gaussian 09, revision D.01; Gaussian, Inc.: Wallingford, CT, 2009.