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Volumn 97, Issue 1, 2013, Pages 141-147

Synthesis and characterization of new electron-withdrawing moiety thieno[2,3-c]pyrrole-4,6-dione-based molecules for small molecule solar cells

Author keywords

Conjugated small molecules; New electron withdrawing moiety; Organic solar cells; Power conversion efficiency; Solution processability; Thieno 2,3 c pyrrole 4,6 dione

Indexed keywords

ELECTRONWITHDRAWING; ORGANIC SOLAR CELL; POWER CONVERSION EFFICIENCIES; PROCESSABILITY; SMALL MOLECULES; THIENO[2,3-C]PYRROLE-4,6-DIONE;

EID: 84872139708     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2012.12.009     Document Type: Article
Times cited : (15)

References (33)
  • 1
    • 73249138888 scopus 로고    scopus 로고
    • Synthesis of conjugated polymers for organic solar cell applications
    • Y.J. Cheng, S.H. Yang, and C.S. Hsu Synthesis of conjugated polymers for organic solar cell applications Chem Rev 109 11 2009 5868 5923
    • (2009) Chem Rev , vol.109 , Issue.11 , pp. 5868-5923
    • Cheng, Y.J.1    Yang, S.H.2    Hsu, C.S.3
  • 2
    • 37549043530 scopus 로고    scopus 로고
    • Polymer-fullerene composite solar cells
    • B.C. Thompson, and J.M. Frechet Polymer-fullerene composite solar cells Angew Chem Int Ed Engl 47 1 2008 58 77
    • (2008) Angew Chem Int Ed Engl , vol.47 , Issue.1 , pp. 58-77
    • Thompson, B.C.1    Frechet, J.M.2
  • 3
    • 67649388867 scopus 로고    scopus 로고
    • A roll-to-roll process to flexible polymer solar cells: Model studies, manufacture and operational stability studies
    • F.C. Krebs, S.A. Gevorgyan, and J. Alstrup A roll-to-roll process to flexible polymer solar cells: model studies, manufacture and operational stability studies J Mater Chem 19 30 2009 5442
    • (2009) J Mater Chem , vol.19 , Issue.30 , pp. 5442
    • Krebs, F.C.1    Gevorgyan, S.A.2    Alstrup, J.3
  • 4
    • 79952632715 scopus 로고    scopus 로고
    • Development of fluorinated benzothiadiazole as a structural unit for a polymer solar cell of 7% efficiency
    • H.X. Zhou, L.Q. Yang, A.C. Stuart, S.C. Price, S.B. Liu, and W. You Development of fluorinated benzothiadiazole as a structural unit for a polymer solar cell of 7% efficiency Angew Chem Int Ed Engl 50 13 2011 2995 2998
    • (2011) Angew Chem Int Ed Engl , vol.50 , Issue.13 , pp. 2995-2998
    • Zhou, H.X.1    Yang, L.Q.2    Stuart, A.C.3    Price, S.C.4    Liu, S.B.5    You, W.6
  • 5
    • 77951907456 scopus 로고    scopus 로고
    • For the bright future-bulk heterojunction polymer solar cells with power conversion efficiency of 7.4%
    • Y.Y. Liang, Z. Xu, J.B. Xia, S.T. Tsai, Y. Wu, and G. Li For the bright future-bulk heterojunction polymer solar cells with power conversion efficiency of 7.4% Adv Mater 22 20 2010 135 138
    • (2010) Adv Mater , vol.22 , Issue.20 , pp. 135-138
    • Liang, Y.Y.1    Xu, Z.2    Xia, J.B.3    Tsai, S.T.4    Wu, Y.5    Li, G.6
  • 6
    • 80054800390 scopus 로고    scopus 로고
    • Simultaneous enhancement of open-circuit voltage, short-circuit current density, and fill factor in polymer solar cells
    • Z.C. He, C.M. Zhong, X. Huang, W.Y. Wong, H.B. Wu, and L.W. Chen Simultaneous enhancement of open-circuit voltage, short-circuit current density, and fill factor in polymer solar cells Adv Mater 23 40 2011 4636 4643
    • (2011) Adv Mater , vol.23 , Issue.40 , pp. 4636-4643
    • He, Z.C.1    Zhong, C.M.2    Huang, X.3    Wong, W.Y.4    Wu, H.B.5    Chen, L.W.6
  • 7
    • 79953043020 scopus 로고    scopus 로고
    • Bulk heterojunction solar cells using thieno[3,4-c]pyrrole-4,6-dione and dithieno[3,2-b:2′,3′-d]silole copolymer with a power conversion efficiency of 7.3%
    • T.Y. Chu, J.P. Lu, S. Beaupre, Y.G. Zhang, J.R. Pouliot, and S. Wakim Bulk heterojunction solar cells using thieno[3,4-c]pyrrole-4,6-dione and dithieno[3,2-b:2′,3′-d]silole copolymer with a power conversion efficiency of 7.3% J Am Chem Soc 133 12 2011 4250 4253
    • (2011) J Am Chem Soc , vol.133 , Issue.12 , pp. 4250-4253
    • Chu, T.Y.1    Lu, J.P.2    Beaupre, S.3    Zhang, Y.G.4    Pouliot, J.R.5    Wakim, S.6
  • 8
    • 70350774564 scopus 로고    scopus 로고
    • Polymer solar cells with enhanced open-circuit voltage and efficiency
    • H.Y. Chen, J.H. Hou, S.Q. Zhang, Y.Y. Liang, G.W. Yang, and Y. Yang Polymer solar cells with enhanced open-circuit voltage and efficiency Nat Photon 3 2009 639 653
    • (2009) Nat Photon , vol.3 , pp. 639-653
    • Chen, H.Y.1    Hou, J.H.2    Zhang, S.Q.3    Liang, Y.Y.4    Yang, G.W.5    Yang, Y.6
  • 9
    • 84862776807 scopus 로고    scopus 로고
    • Tandem polymer solar cells featuring a spectrally matched low-band gap polymer
    • L.T. Dou, J.B. You, J. Yang, C.C. Chen, Y.J. He, and S. Murase Tandem polymer solar cells featuring a spectrally matched low-band gap polymer Nat Photon 6 3 2012 180 186
    • (2012) Nat Photon , vol.6 , Issue.3 , pp. 180-186
    • Dou, L.T.1    You, J.B.2    Yang, J.3    Chen, C.C.4    He, Y.J.5    Murase, S.6
  • 10
    • 84862739175 scopus 로고    scopus 로고
    • Improving the ordering and photovoltaic properties by extending π-conjugated area of electron-donating units in polymers with D-A structure
    • Y. Huang, X. Guo, F. Liu, L.J. Huo, Y.F. Li, and J.H. Hou Improving the ordering and photovoltaic properties by extending π-conjugated area of electron-donating units in polymers with D-A structure Adv Mater 24 25 2012 3383 3389
    • (2012) Adv Mater , vol.24 , Issue.25 , pp. 3383-3389
    • Huang, Y.1    Guo, X.2    Liu, F.3    Huo, L.J.4    Li, Y.F.5    Hou, J.H.6
  • 11
    • 80053474962 scopus 로고    scopus 로고
    • Replacing alkoxy groups with alkylthienyl groups: A feasible approach to improve the properties of photovoltaic polymers
    • L.J. Huo, S.Q. Zhang, X. Guo, F. Xu, Y.F. Li, and J.H. Hou Replacing alkoxy groups with alkylthienyl groups: a feasible approach to improve the properties of photovoltaic polymers Angew Chem Int Ed Engl 50 41 2011 9697 9702
    • (2011) Angew Chem Int Ed Engl , vol.50 , Issue.41 , pp. 9697-9702
    • Huo, L.J.1    Zhang, S.Q.2    Guo, X.3    Xu, F.4    Li, Y.F.5    Hou, J.H.6
  • 12
    • 84863421792 scopus 로고    scopus 로고
    • Absorption enhancement of oligothiophene dyes through the use of a cyanopyridone acceptor group in solution-processed organic solar cells
    • A. Gupta, A. Ali, A. Bilic, M. Gao, K. Hegedus, and B. Singh Absorption enhancement of oligothiophene dyes through the use of a cyanopyridone acceptor group in solution-processed organic solar cells Chem Commun 48 13 2012 1889 1891
    • (2012) Chem Commun , vol.48 , Issue.13 , pp. 1889-1891
    • Gupta, A.1    Ali, A.2    Bilic, A.3    Gao, M.4    Hegedus, K.5    Singh, B.6
  • 14
    • 84859953805 scopus 로고    scopus 로고
    • Small molecule semiconductors for high-efficiency organic photovoltaics
    • Y.Z. Lin, Y.F. Li, and X.W. Zhan Small molecule semiconductors for high-efficiency organic photovoltaics Chem Soc Rev 41 2012 4245 4272
    • (2012) Chem Soc Rev , vol.41 , pp. 4245-4272
    • Lin, Y.Z.1    Li, Y.F.2    Zhan, X.W.3
  • 15
    • 82455210304 scopus 로고    scopus 로고
    • High-performance solar cells using a solution-processed small molecule containing benzodithiophene unit
    • Y.S. Liu, X.J. Wan, F. Wang, J.Y. Zhou, G.K. Long, and J.G. Tian High-performance solar cells using a solution-processed small molecule containing benzodithiophene unit Adv Mater 23 45 2011 5387 5391
    • (2011) Adv Mater , vol.23 , Issue.45 , pp. 5387-5391
    • Liu, Y.S.1    Wan, X.J.2    Wang, F.3    Zhou, J.Y.4    Long, G.K.5    Tian, J.G.6
  • 16
    • 80455132459 scopus 로고    scopus 로고
    • A planar small molecule with dithienosilole core for high efficiency solution-processed organic photovoltaic cells
    • J.Y. Zhou, X.J. Wan, Y.S. Liu, G.K. Long, F. Wang, and Z. Li A planar small molecule with dithienosilole core for high efficiency solution-processed organic photovoltaic cells Chem Mater 23 21 2011 4666 4668
    • (2011) Chem Mater , vol.23 , Issue.21 , pp. 4666-4668
    • Zhou, J.Y.1    Wan, X.J.2    Liu, Y.S.3    Long, G.K.4    Wang, F.5    Li, Z.6
  • 17
    • 84857786555 scopus 로고    scopus 로고
    • Solution processable rhodanine-based small molecule organic photovoltaic cells with a power conversion efficiency of 6.1%
    • Z. Li, G.R. He, X.J. Wan, Y.S. Liu, J.Y. Zhou, and G.K. Long Solution processable rhodanine-based small molecule organic photovoltaic cells with a power conversion efficiency of 6.1% Adv Energy Mater 2 1 2012 74 77
    • (2012) Adv Energy Mater , vol.2 , Issue.1 , pp. 74-77
    • Li, Z.1    He, G.R.2    Wan, X.J.3    Liu, Y.S.4    Zhou, J.Y.5    Long, G.K.6
  • 18
    • 84861460372 scopus 로고    scopus 로고
    • Design and synthesis of carbonyl group modified conjugated polymers for photovoltaic application
    • M.M. Shi, L. Fu, X.L. Hu, L.J. Zuo, D. Deng, and J. Chen Design and synthesis of carbonyl group modified conjugated polymers for photovoltaic application Polym Bull 68 7 2011 1867 1877
    • (2011) Polym Bull , vol.68 , Issue.7 , pp. 1867-1877
    • Shi, M.M.1    Fu, L.2    Hu, X.L.3    Zuo, L.J.4    Deng, D.5    Chen, J.6
  • 19
    • 80054850174 scopus 로고    scopus 로고
    • New diketo-pyrrolo-pyrrole (DPP) sensitizer containing a furan moiety for efficient and stable dye-sensitized solar cells
    • S.Y. Qu, B. Wang, F.L. Guo, J. Li, Wu WenJ, and J.L. Hua New diketo-pyrrolo-pyrrole (DPP) sensitizer containing a furan moiety for efficient and stable dye-sensitized solar cells Dye Pigment 92 2012 1384 1393
    • (2012) Dye Pigment , vol.92 , pp. 1384-1393
    • Qu, S.Y.1    Wang, B.2    Guo, F.L.3    Li, J.4    Wenj, W.5    Hua, J.L.6
  • 20
    • 82155186693 scopus 로고    scopus 로고
    • Solution-processable star-shaped photovoltaic organic molecules based on triphenylamine and benzothiadiazole with longer pi-bridge
    • J. Zhang, J.T. Yu, C. He, D. Deng, Z.G. Zhang, and M.J. Zhang Solution-processable star-shaped photovoltaic organic molecules based on triphenylamine and benzothiadiazole with longer pi-bridge Org Electron 13 1 2012 166 172
    • (2012) Org Electron , vol.13 , Issue.1 , pp. 166-172
    • Zhang, J.1    Yu, J.T.2    He, C.3    Deng, D.4    Zhang, Z.G.5    Zhang, M.J.6
  • 21
    • 84861392564 scopus 로고    scopus 로고
    • D-A-D low band gap molecule containing triphenylamine and benzoxadiazole/benzothiadiazole units: Synthesis and photophysical properties
    • S.H. Zeng, L.X. Yin, X.Y. Jiang, Y.Q. Lia, and K.C. Li D-A-D low band gap molecule containing triphenylamine and benzoxadiazole/benzothiadiazole units: synthesis and photophysical properties Dye Pigment 95 2012 229 235
    • (2012) Dye Pigment , vol.95 , pp. 229-235
    • Zeng, S.H.1    Yin, L.X.2    Jiang, X.Y.3    Lia, Y.Q.4    Li, K.C.5
  • 23
    • 79952667062 scopus 로고    scopus 로고
    • Nanoscale correlation between exciton dissociation and carrier transport in silole-containing cyclopentadithiophene-based bulk heterojunction films
    • J.H. Huang, C.M. Teng, Y.S. Hsiao, F.W. Yen, P. Chen, and F.C. Chang Nanoscale correlation between exciton dissociation and carrier transport in silole-containing cyclopentadithiophene-based bulk heterojunction films J Phys Chem C 115 5 2011 2398 2405
    • (2011) J Phys Chem C , vol.115 , Issue.5 , pp. 2398-2405
    • Huang, J.H.1    Teng, C.M.2    Hsiao, Y.S.3    Yen, F.W.4    Chen, P.5    Chang, F.C.6
  • 24
    • 79952266346 scopus 로고    scopus 로고
    • Conjugated polymers based on C, Si and N-bridged dithiophene and thienopyrroledione units: Synthesis, field-effect transistors and bulk heterojunction polymer solar cells
    • Y. Zhang, J.Y. Zou, H.L. Yip, Y. Sun, J.A. Davies, and K.S. Chen Conjugated polymers based on C, Si and N-bridged dithiophene and thienopyrroledione units: synthesis, field-effect transistors and bulk heterojunction polymer solar cells J Mater Chem 21 11 2011 3895
    • (2011) J Mater Chem , vol.21 , Issue.11 , pp. 3895
    • Zhang, Y.1    Zou, J.Y.2    Yip, H.L.3    Sun, Y.4    Davies, J.A.5    Chen, K.S.6
  • 25
    • 79956367246 scopus 로고    scopus 로고
    • Synthesis, characterization, and photovoltaic property of a low band gap polymer alternating dithienopyrrole and thienopyrroledione units
    • X.L. Hu, M.M. Shi, L.J. Zuo, Y.X. Nan, Y. Liu, and L. Fu Synthesis, characterization, and photovoltaic property of a low band gap polymer alternating dithienopyrrole and thienopyrroledione units Polymer 52 12 2011 2559 2564
    • (2011) Polymer , vol.52 , Issue.12 , pp. 2559-2564
    • Hu, X.L.1    Shi, M.M.2    Zuo, L.J.3    Nan, Y.X.4    Liu, Y.5    Fu, L.6
  • 26
    • 80054906856 scopus 로고    scopus 로고
    • Thienopyrrolyl dione end-capped oligothiophene ambipolar semiconductors for thin film- and light emitting transistors
    • M. Melucci, M. Zambianchi, L. Favaretto, M. Gazzano, A. Zanelli, and M. Monari Thienopyrrolyl dione end-capped oligothiophene ambipolar semiconductors for thin film- and light emitting transistors Chem Commun 47 43 2011 11840 11842
    • (2011) Chem Commun , vol.47 , Issue.43 , pp. 11840-11842
    • Melucci, M.1    Zambianchi, M.2    Favaretto, L.3    Gazzano, M.4    Zanelli, A.5    Monari, M.6
  • 27
    • 79954427655 scopus 로고    scopus 로고
    • Polymer solar cells based on copolymers of dithieno[3,2-b:2′, 3′-d]silole and thienopyrroledione
    • Y.R. Hong, H.K. Wong, L.C. Moh, H.S. Tan, and Z.K. Chen Polymer solar cells based on copolymers of dithieno[3,2-b:2′,3′-d]silole and thienopyrroledione Chem Commun 47 17 2011 4920 4922
    • (2011) Chem Commun , vol.47 , Issue.17 , pp. 4920-4922
    • Hong, Y.R.1    Wong, H.K.2    Moh, L.C.3    Tan, H.S.4    Chen, Z.K.5
  • 28
    • 77951945664 scopus 로고    scopus 로고
    • Efficient polymer solar cells based on the copolymers of benzodithiophene and thienopyrroledione
    • Y. Zhang, S.K. Hau, H.L. Yip, Y. Sun, O. Acton, and A.K.Y. Jen Efficient polymer solar cells based on the copolymers of benzodithiophene and thienopyrroledione Chem Mater 22 9 2010 2696 2698
    • (2010) Chem Mater , vol.22 , Issue.9 , pp. 2696-2698
    • Zhang, Y.1    Hau, S.K.2    Yip, H.L.3    Sun, Y.4    Acton, O.5    Jen, A.K.Y.6
  • 29
    • 35548960124 scopus 로고    scopus 로고
    • Organic thin-film photovoltaic cells based on oligothiophenes with reduced bandgap
    • C. Uhrich, R. Schueppel, A. Petrich, M. Pfeiffer, K. Leo, and E. Brier Organic thin-film photovoltaic cells based on oligothiophenes with reduced bandgap Adv Funct Mater 17 15 2007 2991 2999
    • (2007) Adv Funct Mater , vol.17 , Issue.15 , pp. 2991-2999
    • Uhrich, C.1    Schueppel, R.2    Petrich, A.3    Pfeiffer, M.4    Leo, K.5    Brier, E.6
  • 30
    • 84862308761 scopus 로고    scopus 로고
    • Effect of substituents on the aggregate structure and photovoltaic property of violanthrone derivatives
    • M.M. Shi, F. Hao, L.J. Zuo, Y. Chen, Y.X. Nan, and H.Z. Chen Effect of substituents on the aggregate structure and photovoltaic property of violanthrone derivatives Dye Pigment 95 2012 377 383
    • (2012) Dye Pigment , vol.95 , pp. 377-383
    • Shi, M.M.1    Hao, F.2    Zuo, L.J.3    Chen, Y.4    Nan, Y.X.5    Chen, H.Z.6
  • 32
    • 84867009984 scopus 로고    scopus 로고
    • Improvement of interfacial contacts for new small-molecule bulk-heterojunction organic photovoltaics
    • A. Garcia, G.C. Welch, E.L. Ratcliff, D.S. Ginley, G.C. Bazan, and D.C. Olson Improvement of interfacial contacts for new small-molecule bulk-heterojunction organic photovoltaics Adv Mater 24 39 2012 5368 5373
    • (2012) Adv Mater , vol.24 , Issue.39 , pp. 5368-5373
    • Garcia, A.1    Welch, G.C.2    Ratcliff, E.L.3    Ginley, D.S.4    Bazan, G.C.5    Olson, D.C.6
  • 33
    • 33645392241 scopus 로고    scopus 로고
    • Design rules for donors in bulk-heterojunction solar cells-towards 10% energy-conversion efficiency
    • M.C. Scharber, D. Mühlbacher, M. Koppe, P. Denk, C. Waldauf, and A.J. Heeger Design rules for donors in bulk-heterojunction solar cells-towards 10% energy-conversion efficiency Adv Mater 18 6 2006 789 794
    • (2006) Adv Mater , vol.18 , Issue.6 , pp. 789-794
    • Scharber, M.C.1    Mühlbacher, D.2    Koppe, M.3    Denk, P.4    Waldauf, C.5    Heeger, A.J.6


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