New difluorenylaminocoumarin photosensitizers for dye-sensitized solar cells
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Abstract
Three difluorenylaminocoumarin sensitizers with different π-bridges bearing thiophene ring and cyanoacrylic acid acceptor were synthesized and their photophysical properties and photoelectric conversion efficiency were investigated and compared with counterpart dyes with diphenylaminocoumarin donor. Replacement of benzene with fluorene in the donor unit contributed to superior photovoltaic performance. Among the three π-bridges, the thiophene-phenyl π-bridge improved V OC and J SC, resulting in a DSSC with the best photoelectric conversion efficiency (η = 5.94%, V OC = 670 mV, J SC = 14.53 mA cm−2, and fill factor, FF = 0.61).
Keywords
Triarylamine Coumarin Sensitizers Photoelectric conversionNotes
Acknowledgements
This work was supported by the National Natural Science Foundation of China (21406202).
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References
- 1.R.W. Miles, K.M. Hynes, I. Forbes, Prog. Cryst. Growth Ch. 51, 1 (2005)CrossRefGoogle Scholar
- 2.M.A.M. Al-Alwani, A.B. Mohamad, N.A. Ludin, A.A.H. Kadhum, K. Sopian, Renew. Sustain. Energy Rev. 65, 183 (2016)CrossRefGoogle Scholar
- 3.A. Hafeldt, G. Boschloo, L.C. Sun, L. Kloo, H. Pettersson, Chem. Rev. 110, 6595 (2010)CrossRefGoogle Scholar
- 4.L. Kloo, Chem. Commun. 49, 6580 (2013)CrossRefGoogle Scholar
- 5.Y. Chi, K.L. Wu, T.C. Wei, Chem-Asian J. 10, 1098 (2015)CrossRefGoogle Scholar
- 6.J.F. Huang, J.M. Liu, P.Y. Su, Y.F. Chen, Y. Shen, L.M. Xiao, D.B. Kuang, C.Y. Su, Electrochim. Acta 174, 494 (2015)CrossRefGoogle Scholar
- 7.S. Bezzubov, Y. M. Kiselev, A. V. Churakov, S. A. Kozyukhin, A. A. Sadovnikov, V. A. Grinberg, V. V. Emets, V. D. Doljenko, Eur. J. Inorg. Chem. 347 (2016)Google Scholar
- 8.S.X. Wei, Y. Shao, X.F. Shi, X.Q. Lu, K. Li, Z.G. Zhao, C. Guo, H.Y. Zhu, W.Y. Guo, Org. Electron. 29, 142 (2016)CrossRefGoogle Scholar
- 9.S. Chaurasia, C.J. Liang, Y.S. Yen, J.T. Lin, J. Mater. Chem. C 3, 9765 (2015)CrossRefGoogle Scholar
- 10.Y.Z. Wu, W.H. Zhu, Chem. Soc. Rev. 42, 2039 (2013)CrossRefGoogle Scholar
- 11.C.P. Lee, R.Y.Y. Lin, L.Y. Lin, C.T. Li, T.C. Chu, S.S. Sun, J.T. Lin, K.C. Ho, RSC Adv. 5, 23810 (2015)CrossRefGoogle Scholar
- 12.Y. Wang, Z. Zheng, T. Li, N. Robertson, H. Xiang, W. Wu, J. Hua, W.H. Zhu, H. Tian, ACS Appl. Mater. Interfaces 8, 31016 (2016)CrossRefGoogle Scholar
- 13.L. Han, J. Zhao, B. Wang, S. Jiang, J. Photochem. Photobiol. A 326, 1 (2016)CrossRefGoogle Scholar
- 14.S. Chen, H. Jia, M. Zheng, K. Shen, H. Zheng, Phys. Chem. Chem. Phys. 18, 29555 (2016)CrossRefGoogle Scholar
- 15.Y. Liu, J. He, L. Han, J. Gao, J. Photochem. Photobiol. A 332, 283 (2017)CrossRefGoogle Scholar
- 16.A. Saini, K.R.J. Thomas, C.T. Li, K.C. Ho, J. Mater. Sci. Mater. Electron. 27, 12392 (2016)CrossRefGoogle Scholar
- 17.X.F. Zhang, F.L. Gou, J. Shi, H. Gao, C.L. Xu, Z.P. Zhu, H.W. Jing, RSC Adv. 6, 106380 (2016)CrossRefGoogle Scholar
- 18.L. Han, R. Kang, X. Zu, Y. Cui, J. Gao, Photochem. Photobiol. Sci. 14, 2046 (2015)CrossRefGoogle Scholar
- 19.J.Y. Wang, K. Liu, L.C. Ma, X.W. Zhan, Chem. Rev. 116, 14675 (2016)CrossRefGoogle Scholar
- 20.M. Liang, J. Chen, Chem. Soc. Rev. 42, 3453 (2013)CrossRefGoogle Scholar
- 21.Y.K. Eom, J.Y. Hong, J. Kim, H.K. Kim, Dyes Pigments 136, 496 (2017)CrossRefGoogle Scholar
- 22.H.L. Huang, H.J. Chen, J. Long, G. Wang, S.T. Tan, J. Power Sources 326, 438 (2016)CrossRefGoogle Scholar
- 23.I. Imae, Y. Ito, S. Matsuura, Y. Harima, Org. Electron. 37, 465 (2016)CrossRefGoogle Scholar
- 24.B. Liu, R. Wang, W. Mi, X. Li, H. Yu, J. Mater. Chem. 22, 15379 (2012)CrossRefGoogle Scholar
- 25.C. Zhong, J. Gao, Y. Cui, T. Li, L. Han, J. Power Sources 273, 831 (2015)CrossRefGoogle Scholar
- 26.K. Pan, Y.Z. Dong, C.G. Tian, W. Zhou, G.H. Tian, B.F. Zhao, H.G. Fu, Electrochim. Acta 54, 7350 (2009)CrossRefGoogle Scholar
- 27.L.Y. Lin, C.P. Lee, M.H. Yeh, A. Baheti, R. Vittal, J. Thomas, K.C. Ho, J. Power Sources 215, 122 (2012)CrossRefGoogle Scholar
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