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Synthesis of Conjugated Materials Based on Benzodithiophene - Benzothiadazole and Their Application of Organic Solar Cells

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Abstract

Electron acceptor-donor-acceptor type oligomers based on benzothiadiazole (BT) unit and a (4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl) bis(trimethylstannane) (BDT) unit have been designed and prepared as electron-donating materials, which are 2,6-[5-(7-methyl-benzo[1,2,5]thiadiazol-4-yl)-thiophen-2-yl]-4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b′]dithiophene) (BDT-TBT) and 2,6-[5′-(3′-hexyl-[2,2′]bithiophenyl-5-yl)-7-methyl-benzo[1,2,5]thiadiazole]-4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b′]dithiophene) (BDT-THTBT), for Organic Solar Cells (OSCs) with PC71BM as electron-accepting materials. The HOMO energy level is elevated by the number of thiophene ring as a p-bridge, which lowers the band gap. Inverted-type organic solar cells (OSCs) with a configuration of ITO/ZnO/BDT-TBT (or BDT-THTBT):PC71BM/MoO3/Al are fabricated. OSC based on BDT-THTBT exhibits the highest power conversion efficiency (PCE) of 1.04% with the best J sc of 4.20 mA/cm2.

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References

  1. S. Oh, S. Badgujar, D. H. Kim, W. E. Lee, N. Khan, M. Jahandar, S. Rasool, C. E. Song, H. K. Lee, W. S. Shin, J. C. Lee, S. J. Moon, and S. K. Lee, J. Mater. Chem. A, 5, 15923 (2017).

    Article  CAS  Google Scholar 

  2. Y. Q. Yi, H. Feng, M. Chang, H. Zhang, X. Wan, C. Li, and Y. Chen, J. Mater. Chem. A, 5, 17204 (2017).

    Article  CAS  Google Scholar 

  3. S. Somasundaram, S. Jeon, and S. Park, Macromol. Res., 24, 226 (2016).

    Article  CAS  Google Scholar 

  4. Y.-H. Ha, J. E. Lee, M.-C. Hwang, Y. J. Kim, J.-H. Lee, C. E. Park, and Y.-H. Kim, Macromol. Res., 24, 457 (2016).

    Article  CAS  Google Scholar 

  5. H. Y. Kim, M. H. Choi, Y. W. Han, D. K. Moon, and J. R. Haw, J. Ind. Eng. Chem., 33, 209 (2016).

    Article  CAS  Google Scholar 

  6. N. Gasparini, L. Lucera, M. Salvador, M. Prosa, G. D. Spyropoulus, P. Kubis, H. J. Egeelhaf, C. J. Brabec, and T. Ameri, Energy Environ. Sci., 10, 885 (2017).

    Article  CAS  Google Scholar 

  7. D. Deng, Y. Zhang, J. Zhang, Z. Wang, L. Zhu, J. Fang, B. Xia, Z. Wang, K. Lu, W. Ma, and Z. Wei, Nat. Commun., 7, 13740 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Y. Liu, C. C. Chen, Z. Hong, J. Gao, Y. Yang, H. Zhou, L. Dou, G. Li, and Y. Yang, Sci. Rep., 3, 3356 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  9. R. Xin, J. Feng, C. Zeng, W. Jiang, L. Zhang, D. Meng, Z. Ren, Z. Wang, and S. Yan, ACS Appl. Mater. Interfaces, 9, 2739 (2017).

    Article  CAS  PubMed  Google Scholar 

  10. R. Dominguez, N. F. Montcada, P. Cruz, E. Palomares, and F. Langa, Phys. Chem. Chem. Phys., 19, 3640 (2017).

    Article  CAS  PubMed  Google Scholar 

  11. Q. Zhang, B. Kan, F. Liu, G. Long, X. Wang, X. Chen, Y. Zuo, W. Ni, H. Zhang, M. Li, Z. Hu, F. Huang, Y. Cao, Z. Liang, M. Zhang, T. P. Russell, and Y. Chen, Nat. Photonics, 9, 35 (2015).

    Article  CAS  Google Scholar 

  12. W. Chen and Q. Zhang, J. Mater. Chem. C, 5, 1275 (2017).

    Article  CAS  Google Scholar 

  13. N. Liang, W. Jiang, J. Hou, and Z. Wang, Mater. Chem. Front., 1, 1291 (2017).

    Article  CAS  Google Scholar 

  14. J. Ku, Y. Lansac, Y. H. and J. Jang, Phys. Chem. C, 115, 21508 (2011).

    Article  CAS  Google Scholar 

  15. Y. Eom, C. E. Song, W. S. Shin, S. K. Lee, and E. Lim, J. Ind. Eng. Chem., 45, 338 (2017).

    Article  CAS  Google Scholar 

  16. L. Ye, X. Jiao, H. Zhang, S. Li, H. Yao, H. Ade, and J. Hou, Macromolecules, 48, 7156 (2015).

    Article  CAS  Google Scholar 

  17. H. Yao, L. Ya, H. Zhang, S. Li, S. Zhang, and J. Hou, Chem. Rev., 116, 7397 (2016).

    Article  CAS  PubMed  Google Scholar 

  18. R. K. Pai, T. N. Ahipa, and B. Hemavathi, RSC Adv., 6, 23760 (2016).

    Article  CAS  Google Scholar 

  19. Y. Jeon, T. M. Kim, J. J. Kim, and J. I. Hong, New J. Chem., 39, 9591 (2015).

    Article  CAS  Google Scholar 

  20. M. Karakus, D. H. Apaydin, D. E. Yildiz, L. Toppare, and A. Cirpan, Polymer, 53, 1198 (2012).

    Article  CAS  Google Scholar 

  21. N. Sylvianti, Y. W. Kim, M. A. Marsya, D. K. Moon, and J. H. Kim, Synth. Met., 221, 127 (2016).

    Article  CAS  Google Scholar 

  22. P. Chen, K. Nakano, K. Suzuki, K. Hashimoto, T. Kikitsu, D. Hashizume, T. Koganezawa, and K. Tajima, ACS Appl. Mater. Interfaces, 9, 4758 (2017).

    Article  CAS  PubMed  Google Scholar 

  23. E. Bundgaard and F. C. Krebs, Sol. Energy Mater. Sol. Cells, 91, 954 (2007).

    Article  CAS  Google Scholar 

  24. F. Zhang, D. Wu, Y. Xu, and X. Feng, J. Mater. Chem., 21, 17590 (2011).

    Article  CAS  Google Scholar 

  25. N. V. Elumalai and A. Uddin, Energy Environ. Sci., 9, 391 (2016).

    Article  CAS  Google Scholar 

  26. X. Jiang, Y. Yang, J. Zhu, T. K. Lau, P. Cheng, X. Lu, X. Zhan, and X. Chen, J. Mater. Chem. C, 5, 8179 (2017).

    Article  CAS  Google Scholar 

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Correspondence to Joo Hyun Kim.

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Acknowledgments: This work was supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP) and the Ministry of Trade, Industry & Energy (MOTIE) of the Republic of Korea (No. 20174010201460) and was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2015015683).

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Sylvianti, N., Kim, Y.H., Kim, D.G. et al. Synthesis of Conjugated Materials Based on Benzodithiophene - Benzothiadazole and Their Application of Organic Solar Cells. Macromol. Res. 26, 552–556 (2018). https://doi.org/10.1007/s13233-018-6066-4

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  • DOI: https://doi.org/10.1007/s13233-018-6066-4

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