Tuning the Crystal Polymorphs of Alkyl Thienoacene via Solution Self‐Assembly Toward Air‐Stable and High‐Performance Organic Field‐Effect Transistors

Ping He; Zeyi Tu; Guangyao Zhao; Yonggang Zhen; Hua Geng; Yuanping Yi; Zongrui Wang; Hantang Zhang; Chunhui Xu; Jie Liu; Xiuqiang Lu; Xiaolong Fu; Qiang Zhao; Xiaotao Zhang; Deyang Ji; Lang Jiang; Huanli Dong; Wenping Hu

doi:10.1002/adma.201404806

journal article·2015-02

Tuning the Crystal Polymorphs of Alkyl Thienoacene via Solution Self‐Assembly Toward Air‐Stable and High‐Performance Organic Field‐Effect Transistors

Ping He, Zeyi Tu, Guangyao Zhao, Yonggang Zhen, Hua Geng, Yuanping Yi, Zongrui Wang, Hantang Zhang, Chunhui Xu, Jie Liu, Xiuqiang Lu, Xiaolong Fu, Qiang Zhao, Xiaotao Zhang, Deyang Ji, Lang Jiang, Huanli Dong, Wenping Hu

Advanced Materials· Volume 27· Issue 5

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Source abstract

Abstract

The first example for thienoacene derivatives with selective growth of different crystal polymorphs is simply achieved by solution-phase self-assembly. Compared with platelet-shaped α-phase crystals, organic field-effect transistors (OFETs) based on microribbon-shaped β-phase crystals show a hole mobility up to 18.9 cm(2) V(-1) s(-1), which is one of the highest values for p-type organic semiconductors measured under ambient conditions.

Source: openalex_inverted_index · Quality: baseline

Research context

Electronic materials

OpenAlex topics: Organic Electronics and Photovoltaics · Advanced Memory and Neural Computing · Perovskite Materials and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

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

University of Chinese Academy of Sciences Beijing 100039 P. R. China

References (35)

Show source-provided references

1. 10.1021/ar900228v10.1021/ar900228v ↗

2. 10.1016/S1369-7021(07)70016-010.1016/S1369-7021(07)70016-0 ↗

3. 10.1021/cg301130n10.1021/cg301130n ↗

4. 10.1039/B914334C10.1039/B914334C ↗

5. Wang C. · Appl. Phys. Lett. · 2010 · 96

6. 10.1038/nature1068310.1038/nature10683 ↗

7. 10.1016/S0022-0248(98)00034-710.1016/S0022-0248(98)00034-7 ↗

8. 10.1002/adma.20050135010.1002/adma.200501350 ↗

9. 10.1021/jp045748910.1021/jp0457489 ↗

10. 10.1002/adma.20060207210.1002/adma.200602072 ↗

11. 10.1103/PhysRevB.70.10410610.1103/PhysRevB.70.104106 ↗

12. 10.1002/adma.20070068210.1002/adma.200700682 ↗

13. 10.1021/jz300993p10.1021/jz300993p ↗

14. 10.1063/1.278497010.1063/1.2784970 ↗

15. 10.1002/adma.20100144610.1002/adma.201001446 ↗

16. 10.1002/(SICI)1521-4095(199803)10:5<379::AID-ADMA379>3.0.CO;2-A10.1002/(SICI)1521-4095(199803)10:5<379::AID-ADMA379>3.0.CO;2-A ↗

17. 10.1002/cphc.20080077110.1002/cphc.200800771 ↗

18. 10.1063/1.271829110.1063/1.2718291 ↗

19. 10.1021/ja991651210.1021/ja9916512 ↗

20. 10.1002/adfm.20070000410.1002/adfm.200700004 ↗

21. 10.1038/nmat72610.1038/nmat726 ↗

22. 10.1039/b804317e10.1039/b804317e ↗

23. 10.1038/nature0542710.1038/nature05427 ↗

24. 10.1002/adma.20110200710.1002/adma.201102007 ↗

25. 10.1002/adma.20130434610.1002/adma.201304346 ↗

26. 10.1021/ja064052l10.1021/ja064052l ↗

27. 10.1021/ja074841i10.1021/ja074841i ↗

28. 10.1038/nature1031310.1038/nature10313 ↗

29. 10.1002/adma.20070116710.1002/adma.200701167 ↗

30. 10.1002/adma.20090093410.1002/adma.200900934 ↗

31. 10.1039/c2jm30840a10.1039/c2jm30840a ↗

32. 10.1021/ja052816b10.1021/ja052816b ↗

33. 10.1002/adma.20080034110.1002/adma.200800341 ↗

34. 10.1002/adma.20070214510.1002/adma.200702145 ↗

35. 10.1557/mrs.2012.31310.1557/mrs.2012.313 ↗