journal article·2018-09

Integrating Efficient Optical Gain in High‐Mobility Organic Semiconductors for Multifunctional Optoelectronic Applications

Suqian Ma, Ke Zhou, Mengxiao Hu, Qingyuan Li, Yingjie Liu, Hantang Zhang, Jiangbo Jing, Huanli Dong, Bin Xu, Wenping Hu, Wenjing Tian

Advanced Functional Materials· Volume 28· Issue 36
Publisher page

Abstract

Abstract Simultaneously integrating efficient optical gain and high charge carrier mobility in organic semiconductors for multifunctional optoelectronic applications is challenging. Here, a new thiophene/phenylene derivative, 5,5′‐bis(2,2‐diphenylvinyl)‐bithiophene (BDPV2T), containing an appropriate butterfly molecular configuration in a π‐conjugated structure, is designed to achieve both solid‐state emission and charge transport properties. The prepared BDPV2T crystals exhibit excellent light‐emitting characteristics with a photoluminescence quantum yield of 30%, low light‐amplification threshold of 8 kW cm−2, high optical net gain up to 70 cm−1, and high charge carrier mobility up to 1 cm2 V−1 s−1 in their J‐aggregate single crystals. These BDPV2T single crystal characteristics ensure their application potential for photodetectors, field‐effect transistors, and light‐emitting transistors. High optoelectronic performances are achieved with photoresponsivity of 2.0 × 103 A W−1 and light on/off ratio of 5.4 × 105 in photodetectors, and efficient ambipolar charge transport (µh: 0.14 cm2 V−1 s−1, µe: 0.02 cm2 V−1 s−1) and electroluminescence characteristics in light‐emitting transistors. The remarkably integrated optoelectronic properties of BDPV2T suggest it is a promising candidate for organic multifunctional and electrically pumped laser applications.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research

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Affiliations

State Key Laboratory of Supramolecular Structure and Materials Jilin University Changchun 130012 China

Beijing National Laboratory for Molecular Sciences Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China

Tianjin Key Laboratory of Molecular Optoelectronic Sciences Department of Chemistry School of Science Tianjin University & Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) Tianjin 300072 China

Funding

National Natural Science Foundation of China · People's Government of Jilin Province · Ministry of Science and Technology of the People's Republic of China

References (52)

Show source-provided references
1. 10.1002/978352765345410.1002/9783527653454 ↗
2. 10.1039/C1CS15205J10.1039/C1CS15205J ↗
3. 10.1002/adma.20130434610.1002/adma.201304346 ↗
4. 10.1038/1639310.1038/16393 ↗
5. 10.1038/nature1168710.1038/nature11687 ↗
6. 10.1021/cr050152i10.1021/cr050152i ↗
7. 10.1002/(SICI)1521-4095(199903)11:5<363::AID-ADMA363>3.0.CO;2-Y10.1002/(SICI)1521-4095(199903)11:5<363::AID-ADMA363>3.0.CO;2-Y ↗
8. 10.1103/PhysRevB.66.03532110.1103/PhysRevB.66.035321 ↗
9. 10.1039/C4FD00202D10.1039/C4FD00202D ↗
10. 10.1063/1.291243310.1063/1.2912433 ↗
11. 10.1002/adma.20060090110.1002/adma.200600901 ↗
12. 10.1038/nmat169910.1038/nmat1699 ↗
13. 10.1002/1521-4095(200107)13:14<1053::AID-ADMA1053>3.0.CO;2-710.1002/1521-4095(200107)13:14<1053::AID-ADMA1053>3.0.CO;2-7 ↗
14. 10.1021/ja973761j10.1021/ja973761j ↗
15. 10.1201/978142000801210.1201/9781420008012 ↗
16. 10.1126/science.109419610.1126/science.1094196 ↗
17. 10.1002/adma.20130251410.1002/adma.201302514 ↗
18. 10.1002/adma.20060092910.1002/adma.200600929 ↗
19. 10.1021/ja063755010.1021/ja0637550 ↗
20. 10.1002/adma.20090405610.1002/adma.200904056 ↗
21. 10.1021/jp057368910.1021/jp0573689 ↗
22. 10.1002/anie.20110818410.1002/anie.201108184 ↗
23. 10.1021/acs.chemmater.7b0005610.1021/acs.chemmater.7b00056 ↗
24. 10.1002/adfm.20110078310.1002/adfm.201100783 ↗
25. 10.1002/adfm.20090002810.1002/adfm.200900028 ↗
26. 10.1002/adma.20100379710.1002/adma.201003797 ↗
27. 10.1038/nmat216510.1038/nmat2165 ↗
28. 10.1038/ncomms1003210.1038/ncomms10032 ↗
29. 10.1002/adom.20150053110.1002/adom.201500531 ↗
30. 10.1002/lpor.20130022210.1002/lpor.201300222 ↗
31. 10.1021/cr100380z10.1021/cr100380z ↗
32. 10.1021/ja054358c10.1021/ja054358c ↗
33. 10.1002/adma.20130363910.1002/adma.201303639 ↗
34. 10.1002/anie.20130848610.1002/anie.201308486 ↗
35. 10.1021/acs.chemmater.5b0228010.1021/acs.chemmater.5b02280 ↗
36. 10.1039/C0JM02290J10.1039/C0JM02290J ↗
37. 10.1021/jacs.7b0938110.1021/jacs.7b09381 ↗
38. 10.1002/anie.20160278110.1002/anie.201602781 ↗
39. 10.1038/ncomms616210.1038/ncomms6162 ↗
40. 10.1038/nature1031310.1038/nature10313 ↗
41. 10.1021/acs.accounts.6b0057610.1021/acs.accounts.6b00576 ↗
42. 10.1351/pac19651103037110.1351/pac196511030371 ↗
43. 10.1021/ar900233v10.1021/ar900233v ↗
44. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
45. 10.1002/1521-4095(200011)12:22<1655::AID-ADMA1655>3.0.CO;2-210.1002/1521-4095(200011)12:22<1655::AID-ADMA1655>3.0.CO;2-2 ↗
46. 10.1021/cm801427s10.1021/cm801427s ↗
47. 10.1002/adfm.20080029910.1002/adfm.200800299 ↗
48. 10.1021/ar900228v10.1021/ar900228v ↗
49. 10.1021/ja064236010.1021/ja0642360 ↗
50. 10.1038/nature0337610.1038/nature03376 ↗
51. 10.1039/c2cp41712j10.1039/c2cp41712j ↗
52. 10.1039/c3tc32206h10.1039/c3tc32206h ↗