Citation: Liu Qingqing, Zhang Yihan, Gao Can, Wang Tianyu, Hu Wenping, Dong Huanli. Synthesis and Property Study of Field-effect Emissive Conjugated Polymers Based on Styrene and Benzothiadiazole[J]. Acta Chimica Sinica, ;2020, 78(9): 945-953. doi: 10.6023/A20050170 shu

Synthesis and Property Study of Field-effect Emissive Conjugated Polymers Based on Styrene and Benzothiadiazole

  • Corresponding author: Dong Huanli, dhl522@iccas.ac.cn
  • Received Date: 16 May 2020
    Available Online: 24 June 2020

    Fund Project: Beijing National Laboratory for Molecular Sciences BNLMS-CXXM-202012the National Natural Science Foundation of China 51725304Project supported by the National Key Research and Development Project (Nos. 2017YFA0204503, 2018YFA0703200), the National Natural Science Foundation of China (Nos. 61890943, 51725304) and Beijing National Laboratory for Molecular Sciences (BNLMS-CXXM-202012)the National Natural Science Foundation of China 61890943the National Key Research and Development Project 2018YFA0703200the National Key Research and Development Project 2017YFA0204503

Figures(7)

  • Conjugated polymer materials with good photoelectric performance, solution processing ability and flexibility are widely used as active layers in optoelectronic devices. Here, using Stille and Suzuki coupling reactions, we designed and synthesized two new conjugated polymers, poly(1,2-bis(2,5-bis(iso-octyloxy)phenylenevinylene-2,1,3-benzothiadiazole)) (PVBT) and poly(1,2-bis(2,5-bis(n-octyloxy)phenylenevinylene-2,1,3-benzothiadiazole)) (nPVBT), which contain structural element styrene fragments and an conjugated unit benzothiadiazole. Styrene fragments are conducive to luminescent properties of materials, such as phenylenevinylene (PPV) derivatives, while benzothiadiazole unit is electron withdrawing, and matches with many structural units of a donor. The conjugated polymers were characterized by gel permeation chromatography (GPC), elemental analysis and differential scanning calorimetry (DSC). The results indicate that each of these two polymers has good thermal stability. Their melting points were around 240~250℃ and decomposition temperatures around 380℃. Due to the presence of the structural alkoxy chains, these two polymers exhibit good solubility, which is conducive to solution-processed film formation. PVBT and nPVBT have strong fluorescence characters with maximum emission in the range of 590~605 nm. The photoluminescence quantum yield of these two polymers in dichloromethane solution (1×10-5 mol·L-1) is 23%~35%, and 12%~20% in solid films, which are annealed at 180℃ for 10 min. Due to benzothiadiazole's regulation of molecular energy levels, the highest occupied molecular orbital (HOMO) energy level of PVBT and nPVBT were modulated to be -5.73 and -5.61 eV, and the lowest unoccupied molecular orbital (LUMO) energy level were -3.37 and -3.32 eV, respectively. Typical p-type transporting property was determined by using PVBT and nPVBT films as active layers in organic field effect transistors. Because of the improved conjugation of the skeleton structures and the close packing between benzothiadiazole of main chains, these two conjugated polymers both exhibit efficient charge transport characteristics with saturation hole carrier mobility is up to 1.1×10-4 cm2·V-1·s-1 and high switching on/off ratio of 103~104. This work provides new insight into the development of high-performance optoelectronic conjugated polymer materials and sheds light on the research of organic optoelectronic integrated devices.
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    1. [1]

      Huang, F.; Bo, Z. S.; Geng, Y. H.; Wang, X. H.; Wang, L. X.; Ma, Y. G.; Hou, J. H.; Hu, W. P.; Pei, J.; Dong, H. L.; Wang, S.; Li, Z.; Shuai, Z. G.; Li, Y. F.; Cao, Y. Acta Polym. Sin. 2019, 50, 988(in Chinese).
       

    2. [2]

      Dong, H. L.; Fu, X. L.; Liu, J.; Wang, Z. R.; Hu, W. P. Adv. Mater. 2013, 25, 6158.  doi: 10.1002/adma.201302514

    3. [3]

      Xu, Y.; Yao, H. F.; Hou, J. H. Chin. J. Chem. 2019, 37, 207(in Chinese).
       

    4. [4]

      Yang, C. Y.; Jin, W. L.; Wang, J.; Ding, Y. F.; Nong, S.; Shi, K.; Lu, Y.; Dai, Y. Z.; Zhuang, F. D.; Lei, T.; Di, C. A.; Zhu, D. B.; Wang, J. Y.; Pei, J. Adv. Mater. 2018, 30, 1802850.  doi: 10.1002/adma.201802850

    5. [5]

      Li, Q. Q.; Li, Z. Acc. Chem. Res. 2020, 53, 962.  doi: 10.1021/acs.accounts.0c00060

    6. [6]

      Thomas, T. H.; Harkin, D. J.; Gillett, A. J.; Lemaur, V.; Nikolka, M.; Sadhanala, A.; Richter, J. M.; Armitage, J.; Chen, H.; McCulloch, I.; Menke, S. M.; Olivier, Y.; Beljonne, D.; Sirringhaus, H. Nat. Commun. 2019, 10, 2614.  doi: 10.1038/s41467-019-10277-y

    7. [7]

      Feng, L. L.; Gu, P. C.; Dong, H. L.; Yao, Y. F.; Hu, W. P. Chin. Sci. Bull. 2015, 60, 2169(in Chinese).
       

    8. [8]

      Ren, X. C.; Yang, F. X.; Gao, X.; Cheng, S. S.; Zhang, X. T.; Dong, H. L.; Hu, W. P. Adv. Energy Mater. 2018, 8, 1801003.  doi: 10.1002/aenm.201801003

    9. [9]

      Zheng, Z.; Ni, Z. J.; Zhang, X. T.; Zhen, Y. G.; Dong, H. L.; Zhang, J.; Hu, W. P. Sci. China Mater. 2019, 62, 813(in Chinese).
       

    10. [10]

      Ni, Z. J.; Dong, H. L.; Wang, H. L.; Ding, S.; Zou, Y.; Zhao, Q.; Zhen, Y. G.; Liu, F.; Jiang, L.; Hu, W. P. Adv. Mater. 2018, 30, 1704843.  doi: 10.1002/adma.201704843

    11. [11]

      Ni, Z. J.; Wang, H. L.; Dong, H. L.; Dang, Y. F.; Zhao, Q.; Zhang, X. T.; Hu, W. P. Nat. Chem. 2019, 11, 271.  doi: 10.1038/s41557-018-0200-y

    12. [12]

      Guo, Y. L. Acta Polym. Sin. 2020, 51, 448(in Chinese).
       

    13. [13]

      Yao, Y. F.; Dong, H. L.; Liu, F.; Russell, T. P.; Hu, W. P. Adv. Mater. 2017, 29, 1701251.  doi: 10.1002/adma.201701251

    14. [14]

      Zhao, S.; Zhu, R. Acta Chim. Sinica 2019, 77, 1250(in Chinese).
       

    15. [15]

      Qiu, G. G.; Jiang, Z. Y.; Ni, Z. J.; Wang, H. L.; Dong, H. L.; Zhang, J. Q.; Zhang, X. T.; Shu, Z. B.; Lu, K.; Zhen, Y. G.; Wei, Z. X.; Hu, W. P. J. Mater. Chem. C 2017, 5, 566.  doi: 10.1039/C6TC04271F

    16. [16]

      Gu, P. C.; Hu, M. X.; Ding, S.; Zhao, G. Y.; Yao, Y. F.; Liu, F.; Zhang, X. T.; Dong, H. L.; Wang, X. K.; Hu, W. P. Chinese Chem. Lett. 2018, 29, 1675(in Chinese).
       

    17. [17]

      Li, C. G.; Wang, Y. S.; Zou, Y.; Zhang, X. T.; Dong, H. L.; Hu, W. P. Angew. Chem. Int. Ed. 2020, 59, 9403.  doi: 10.1002/anie.202002644

    18. [18]

      Mei, J.; Leung, N. L.; Kwok, R. T.; Lam, J. W.; Tang, B. Z. Chem. Rev. 2015, 115, 11718.  doi: 10.1021/acs.chemrev.5b00263

    19. [19]

      Dong, H. L.; Yan, Q. Q.; Hu, W. P. Acta Polym. Sin. 2017, 8, 1246(in Chinese).
       

    20. [20]

      Qian, X.; Su, M.; Li, F. Y.; Song, Y. L. Acta Chim. Sinica 2016, 74, 565(in Chinese).
       

    21. [21]

      Xu, X. N.; Han, B.; Yu, X.; Zhu, Y. Y. Acta Chim. Sinica 2019, 77, 485(in Chinese).
       

    22. [22]

      Zhang, Y. H.; Ye, J.; Liu, Z. Y.; Liu, Q. Q.; Guo, X. F.; Dang, Y. F.; Zhang, J. Q.; Wei, Z. X.; Wang, Z. X.; Wang, Z. H.; Dong, H. L.; Hu, W. P. J. Mater. Chem. C 2020, DOI:10.1039/D0TC01174F.  doi: 10.1039/D0TC01174F

    23. [23]

      Fu, Y.; Wang, F.; Zhang, Y.; Fang, X.; Lai, W. Y.; Huang, W. Acta Chim. Sinica 2014, 72, 158(in Chinese).
       

    24. [24]

      Wang, Z. W.; Guo, S. J.; Li, H. W.; Wang, B.; Sun, Y. T.; Xu, Z. Y.; Chen, X. S.; Wu, K. J.; Zhang, X. T.; Xing, F. F.; Li, L. Q.; Hu, W. P. Adv. Mater. 2019, 31, 1805630.
       

    25. [25]

      Hepp, A.; Heil, H.; Weise, W.; Ahles, M.; Schmechel, R.; Seggern, H. V. Phys. Rev. Lett. 2003, 91, 157406.  doi: 10.1103/PhysRevLett.91.157406

    26. [26]

      Zhang, C. C.; Chen, P. L.; Hu, W. P. Small 2016, 12, 1252.  doi: 10.1002/smll.201502546

    27. [27]

      Muhieddine, K.; Ullah, M.; Pal, B. N.; Burn, P.; Namdas, E. B. Adv. Mater. 2014, 26, 6410.  doi: 10.1002/adma.201400938

    28. [28]

      Qin, Z. S.; Gao, H. K.; Liu, J. Y.; Zhou, K.; Li, J.; Dang, Y. Y.; Huang, L.; Deng, H. X.; Zhang, X. T.; Dong, H. L.; Hu, W. P. Adv. Mater. 2019, 31, 1903175.  doi: 10.1002/adma.201903175

    29. [29]

      Liu, C. F.; Liu, X.; Lai, W. Y.; Huang, W. Adv. Mater. 2018, 30, 1802466.  doi: 10.1002/adma.201802466

    30. [30]

      Ma, Y. G.; Shen, J. C. Sci. Sin. Chim. 2007, 37, 105(in Chinese).
       

    31. [31]

      Zhang, X. T.; Dong, H. L.; Hu, W. P. Adv. Mater. 2018, 30, 1801048.  doi: 10.1002/adma.201801048

    32. [32]

      Xie, Z. Y.; Liu, D.; Zhang, Y. H.; Liu, Q. Q.; Dong, H. L.; Hu, W. P. Chem. J. Chin. Univ. 2020, 41, 1179(in Chinese).
       

    33. [33]

      Liu, D.; De, J. B.; Gao, H. K.; Ma, S. Q.; Ou, Q.; Li, S.; Qin, Z. S.; Dong, H. L.; Liao, Q.; Xu, B.; Peng, Q.; Shuai, Z. G.; Tian, W. J.; Fu, H. B.; Zhang, X. T.; Zhen, Y. G.; Hu, W. P. J. Am. Chem. Soc. 2020, 142, 6332.  doi: 10.1021/jacs.0c00871

    34. [34]

      Liu, H. C.; Yao, L.; Li, B.; Chen, X. K.; Gao, Y.; Zhang, S. T.; Li, W. J.; Lu, P.; Yang, B.; Ma, Y. G. Chem. Commun. 2016, 52, 7356.  doi: 10.1039/C6CC01993E

    35. [35]

      Chen, M. Y.; Zhao, Y.; Yan, L. J.; Yang, S.; Zhu, Y. N.; Murtaza, I.; He, G. F.; Meng, H.; Huang, W. Angew. Chem. Int. Ed. 2016, 128, 1.  doi: 10.1002/ange.201510990

    36. [36]

      Chen, Z. K.; Lee, N. H. S.; Huang, W. Macromolecules 2003, 36, 1009.  doi: 10.1021/ma021221n

    37. [37]

      Burroughes, J. H.; Bradley, D. D. C.; Brown, A.; Marks, R. R.N.; Mackay, K.; Friend, R. H.; Burnst, P. L.; Holmest A. B. Nature 1990, 347, 539.  doi: 10.1038/347539a0

    38. [38]

      Yu, G.; Gao, J.; Hummelen, J. C.; Wudl, F.; Heeger, A. J. Science 1995, 270, 1789.  doi: 10.1126/science.270.5243.1789

    39. [39]

      Tessler, N.; Denton, G. J.; Friend, R. H. Nature 1996, 382, 695.  doi: 10.1038/382695a0

    40. [40]

      Zaumseil, J.; Friend, R. H.; Sirringhaus, H. Nat. Mater. 2006, 5, 69.  doi: 10.1038/nmat1537

    41. [41]

      Gambino, S.; Bansal, A. K.; Samuel, I. D. W. Org. Electron. 2013, 14, 1980.  doi: 10.1016/j.orgel.2013.03.038

    42. [42]

      Johansson, D. M.; Theander, M.; Srdanov, G.; Yu, G.; Inganas, O.; Andersson, M. R. Macromolecules 2001, 34, 3716.  doi: 10.1021/ma001921x

    43. [43]

      Anant, P.; Lucas, N. T.; Jacob, J. Org. Lett. 2008, 10, 5533.  doi: 10.1021/ol8022837

    44. [44]

      Zhang, W. M.; Smith, J.; Watkins, S. E.; Gysel, R.; McGehee M.; Salleo, A.; Kirkpatrick, J.; Ashraf, S.; Anthopoulos, T.; Heeney, M.; McCulloch, I. J. Am. Chem. Soc. 2010, 132, 11437.  doi: 10.1021/ja1049324

    45. [45]

      Wen, S. P.; Pei, J. N.; Zhou, Y. H.; Li, P. F.; X, L. L.; Li, Y. W.; Xu, B.; Tian, W. J. Macromolecules 2009, 42, 4977.  doi: 10.1021/ma900598c

    46. [46]

      Gwinner, M. C.; Kabra, D.; Roberts, M.; Brenner, T. J. K.; Wallikewitz, B. H.; McNeill, C. R.; Friend, R. H.; Sirringhaus, H. Adv. Mater. 2012, 24, 2728.  doi: 10.1002/adma.201104602

    47. [47]

      Lei, T.; Dou, J. H.; Pei, J. Adv. Mater. 2012, 24, 6457.  doi: 10.1002/adma.201202689

    48. [48]

      Shahid, M.; Ashraf, R. S.; Klemm, E.; Sensfuss, S. Macromolecules 2006, 39, 7844.  doi: 10.1021/ma061231e

    49. [49]

      Li, Y. F.; Cao, Y.; Gao, J.; Wang, D. L.; Yu, G.; Heeger, A. J. Synthetic Met. 1999, 99, 243.  doi: 10.1016/S0379-6779(99)00007-7

    50. [50]

      Sirringhaus, H. Adv. Mater. 2014, 26, 1319.  doi: 10.1002/adma.201304346

    51. [51]

      Rivnay, J. M. S. C.; Miller, C. E.; Salleo, A.; Toney, M. F. Chem. Rev. 2012, 112, 5488.  doi: 10.1021/cr3001109

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