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Volumn 7, Issue 4, 2014, Pages 2411-2439

Polythiophenes comprising conjugated pendants for polymer solar cells: A review

Author keywords

Conjugated pendants; Energy level engineering; Polymer solar cells; Polythiophene

Indexed keywords

ELECTRON ENERGY LEVELS; OPEN CIRCUIT VOLTAGE; POLYMERS; SOLAR CELLS; SULFUR COMPOUNDS;

EID: 84899156316     PISSN: None     EISSN: 19961944     Source Type: Journal    
DOI: 10.3390/ma7042411     Document Type: Review
Times cited : (65)

References (97)
  • 2
    • 84866405451 scopus 로고    scopus 로고
    • Enhanced power-conversion efficiency in polymer solar cells using an inverted device structure
    • He, Z.; Zhong, C.; Su, S.; Xu, M.; Wu, H.; Cao, Y. Enhanced power-conversion efficiency in polymer solar cells using an inverted device structure. Nat. Photon. 2012, 6, 593-597.
    • (2012) Nat. Photon. , vol.6 , pp. 593-597
    • He, Z.1    Zhong, C.2    Su, S.3    Xu, M.4    Wu, H.5    Cao, Y.6
  • 4
    • 0029483704 scopus 로고
    • Polymer photovoltaic cells: Enhanced efficiencies via a network of internal donor-acceptor heterojunctions
    • Yu, G.; Gao, J.; Hummelen, J.C.; Wudl, F.; Heeger, A.J. Polymer photovoltaic cells: Enhanced efficiencies via a network of internal donor-acceptor heterojunctions. Science 1995, 270, 1789-1790.
    • (1995) Science , vol.270 , pp. 1789-1790
    • Yu, G.1    Gao, J.2    Hummelen, J.C.3    Wudl, F.4    Heeger, A.J.5
  • 6
    • 34250901082 scopus 로고    scopus 로고
    • A high-mobility electron-transport polymer with broad absorption and its use in field-effect transistors and all-polymer solar cells
    • Zhan, X.; Tan, Z.A.; Domercq, B.; An, Z.; Zhang, X.; Barlow, S.; Li, Y.; Zhu, D.; Kippelen, B.; Marder, S.R. A high-mobility electron-transport polymer with broad absorption and its use in field-effect transistors and all-polymer solar cells. J. Am. Chem. Soc. 2007, 129, 7246-7247.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 7246-7247
    • Zhan, X.1    Tan, Z.A.2    Domercq, B.3    An, Z.4    Zhang, X.5    Barlow, S.6    Li, Y.7    Zhu, D.8    Kippelen, B.9    Marder, S.R.10
  • 8
    • 0022594397 scopus 로고
    • Two-layer organic photovoltaic cell
    • Tang, C.W. Two-layer organic photovoltaic cell. Appl. Phys. Lett. 1986, 48, 183-185.
    • (1986) Appl. Phys. Lett. , vol.48 , pp. 183-185
    • Tang, C.W.1
  • 9
    • 0030147807 scopus 로고    scopus 로고
    • The exciton binding energy in luminescent conjugated polymers
    • Brédas, J.L.; Cornil, J.; Heeger, A.J. The exciton binding energy in luminescent conjugated polymers. Adv. Mater. 1996, 8, 447-452.
    • (1996) Adv. Mater. , vol.8 , pp. 447-452
    • Brédas, J.L.1    Cornil, J.2    Heeger, A.J.3
  • 10
    • 0037706312 scopus 로고    scopus 로고
    • Why is exciton dissociation so efficient at the interface between a conjugated polymer and an electron acceptor?
    • Arkhipov, V.I.; Heremans, P.; Bässler, H. Why is exciton dissociation so efficient at the interface between a conjugated polymer and an electron acceptor? Appl. Phys. Lett. 2003, 82, 4605-4607.
    • (2003) Appl. Phys. Lett. , vol.82 , pp. 4605-4607
    • Arkhipov, V.I.1    Heremans, P.2    Bässler, H.3
  • 12
    • 79961089735 scopus 로고    scopus 로고
    • Photoconductivity measurements of the electronic structure of organic solar cells
    • doi:10.1103/PhysRevB.83.165207
    • Street, R.; Song, K.; Northrup, J.; Cowan, S. Photoconductivity measurements of the electronic structure of organic solar cells. Phys. Rev. B 2011, 83, doi:10.1103/PhysRevB.83.165207.
    • (2011) Phys. Rev. B , vol.83
    • Street, R.1    Song, K.2    Northrup, J.3    Cowan, S.4
  • 13
    • 66149116003 scopus 로고    scopus 로고
    • Recent progress in polymer solar cells: Manipulation of polymer: Fullerene morphology and the formation of efficient inverted polymer solar cells
    • Chen, L.M.; Hong, Z.; Li, G.; Yang, Y. Recent progress in polymer solar cells: Manipulation of polymer: Fullerene morphology and the formation of efficient inverted polymer solar cells. Adv. Mater. 2009, 21, 1434-1449.
    • (2009) Adv. Mater. , vol.21 , pp. 1434-1449
    • Chen, L.M.1    Hong, Z.2    Li, G.3    Yang, Y.4
  • 14
    • 84857546405 scopus 로고    scopus 로고
    • Recent advances in solution-processed interfacial materials for efficient and stable polymer solar cells
    • Yip, H.L.; Jen, A.K.Y. Recent advances in solution-processed interfacial materials for efficient and stable polymer solar cells. Energy Environ. Sci. 2012, 5, 5994-6011.
    • (2012) Energy Environ. Sci. , vol.5 , pp. 5994-6011
    • Yip, H.L.1    Jen, A.K.Y.2
  • 15
    • 80052169156 scopus 로고    scopus 로고
    • High-performance and highly durable inverted organic photovoltaics embedding solution-processable vanadium oxides as an interfacial hole-transporting layer
    • Chen, C.P.; Chen, Y.D.; Chuang, S.C.; Chen, C.P.; Chen, Y.D.; Chuang, S.C. High-performance and highly durable inverted organic photovoltaics embedding solution-processable vanadium oxides as an interfacial hole-transporting layer. Adv. Mater. 2011, 23, 3859-3863.
    • (2011) Adv. Mater. , vol.23 , pp. 3859-3863
    • Chen, C.P.1    Chen, Y.D.2    Chuang, S.C.3    Chen, C.P.4    Chen, Y.D.5    Chuang, S.C.6
  • 17
    • 33845453438 scopus 로고    scopus 로고
    • Highly efficient inverted organic photovoltaics using solution based titanium oxide as electron selective contact
    • 233517:1-233517:3
    • Waldauf, C.; Morana, M.; Denk, P.; Schilinsky, P.; Coakley, K.; Choulis, S.A.; Brabec, C.J. Highly efficient inverted organic photovoltaics using solution based titanium oxide as electron selective contact. Appl. Phys. Lett. 2006, 89, 233517:1-233517:3.
    • (2006) Appl. Phys. Lett. , vol.89
    • Waldauf, C.1    Morana, M.2    Denk, P.3    Schilinsky, P.4    Coakley, K.5    Choulis, S.A.6    Brabec, C.J.7
  • 18
    • 57649119103 scopus 로고    scopus 로고
    • High performance ambient processed inverted polymer solar cells through interfacial modification with a fullerene self-assembled monolayer
    • 233304:1-233304:3
    • Hau, S.K.; Yip, H.L.; Ma, H.; Jen, A.K.Y. High performance ambient processed inverted polymer solar cells through interfacial modification with a fullerene self-assembled monolayer. Appl. Phys. Lett. 2008, 93, 233304:1-233304:3.
    • (2008) Appl. Phys. Lett. , vol.93
    • Hau, S.K.1    Yip, H.L.2    Ma, H.3    Jen, A.K.Y.4
  • 19
    • 33645392241 scopus 로고    scopus 로고
    • Design rules for donors in bulk-heterojunction solar cells-towards 10% energy-conversion efficiency
    • Scharber, M.C.; Mühlbacher, D.; Koppe, M.; Denk, P.; Waldauf, C.; Heeger, A.J.; Brabec, C.J. Design rules for donors in bulk-heterojunction solar cells-towards 10% energy-conversion efficiency. Adv. Mater. 2006, 18, 789-794.
    • (2006) Adv. Mater. , vol.18 , pp. 789-794
    • Scharber, M.C.1    Mühlbacher, D.2    Koppe, M.3    Denk, P.4    Waldauf, C.5    Heeger, A.J.6    Brabec, C.J.7
  • 20
    • 84890130430 scopus 로고    scopus 로고
    • 25th anniversary article: A decade of organic/polymeric photovoltaic research
    • Dou, L.; You, J.; Hong, Z.; Xu, Z.; Li, G.; Street, R.A.; Yang, Y. 25th anniversary article: A decade of organic/polymeric photovoltaic research. Adv. Mater. 2013, 25, 6642-6671.
    • (2013) Adv. Mater. , vol.25 , pp. 6642-6671
    • Dou, L.1    You, J.2    Hong, Z.3    Xu, Z.4    Li, G.5    Street, R.A.6    Yang, Y.7
  • 21
    • 73249138888 scopus 로고    scopus 로고
    • Synthesis of conjugated polymers for organic solar cell applications
    • Cheng, Y.J.; Yang, S.H.; Hsu, C.S. Synthesis of conjugated polymers for organic solar cell applications. Chem. Rev. 2009, 109, 5868-5923.
    • (2009) Chem. Rev. , vol.109 , pp. 5868-5923
    • Cheng, Y.J.1    Yang, S.H.2    Hsu, C.S.3
  • 22
    • 84862909277 scopus 로고    scopus 로고
    • Rational design of high performance conjugated polymers for organic solar cells
    • Zhou, H.; Yang, L.; You, W. Rational design of high performance conjugated polymers for organic solar cells. Macromolecules 2012, 45, 607-632.
    • (2012) Macromolecules , vol.45 , pp. 607-632
    • Zhou, H.1    Yang, L.2    You, W.3
  • 23
    • 84860351735 scopus 로고    scopus 로고
    • Molecular design of photovoltaic materials for polymer solar cells: Toward suitable electronic energy levels and broad absorption
    • Li, Y. Molecular design of photovoltaic materials for polymer solar cells: Toward suitable electronic energy levels and broad absorption. Acc. Chem. Res. 2012, 45, 723-733.
    • (2012) Acc. Chem. Res. , vol.45 , pp. 723-733
    • Li, Y.1
  • 24
    • 34247359132 scopus 로고    scopus 로고
    • Low band gap polymers for organic photovoltaics
    • Bundgaard, E.; Krebs, F.C. Low band gap polymers for organic photovoltaics. Sol. Energ. Mater. Sol. Cells 2007, 91, 954-985.
    • (2007) Sol. Energ. Mater. Sol. Cells , vol.91 , pp. 954-985
    • Bundgaard, E.1    Krebs, F.C.2
  • 27
  • 28
    • 0021093572 scopus 로고
    • Chain-length dependence of electronic and electrochemical properties of conjugated systems: Polyacetylene, polyphenylene, polythiophene, and polypyrrole
    • Bredas, J.; Silbey, R.; Boudreaux, D.; Chance, R. Chain-length dependence of electronic and electrochemical properties of conjugated systems: Polyacetylene, polyphenylene, polythiophene, and polypyrrole. J. Am. Chem. Soc. 1983, 105, 6555-6559.
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 6555-6559
    • Bredas, J.1    Silbey, R.2    Boudreaux, D.3    Chance, R.4
  • 29
    • 4243893235 scopus 로고
    • Conjugated poly (thiophenes): Synthesis, functionalization, and applications
    • Roncali, J. Conjugated poly (thiophenes): Synthesis, functionalization, and applications. Chem. Rev. 1992, 92, 711-738.
    • (1992) Chem. Rev. , vol.92 , pp. 711-738
    • Roncali, J.1
  • 30
    • 0031700973 scopus 로고    scopus 로고
    • The chemistry of conducting polythiophenes
    • McCullough, R.D. The chemistry of conducting polythiophenes. Adv. Mater. 1998, 10, 93-116.
    • (1998) Adv. Mater. , vol.10 , pp. 93-116
    • McCullough, R.D.1
  • 31
    • 53549127275 scopus 로고    scopus 로고
    • Advances in molecular design and synthesis of regioregular polythiophenes
    • Osaka, I.; McCullough, R.D. Advances in molecular design and synthesis of regioregular polythiophenes. Acc. Chem. Res. 2008, 41, 1202-1214.
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1202-1214
    • Osaka, I.1    McCullough, R.D.2
  • 32
    • 34548662852 scopus 로고    scopus 로고
    • Molecular engineering of the band gap of p-conjugated systems: Facing technological applications
    • Roncali, J. Molecular engineering of the band gap of p-conjugated systems: Facing technological applications. Macromol. Rapid Commun. 2007, 28, 1761-1775.
    • (2007) Macromol. Rapid Commun. , vol.28 , pp. 1761-1775
    • Roncali, J.1
  • 33
    • 84892619127 scopus 로고    scopus 로고
    • Side chain engineering in solution-processable conjugated polymers
    • Mei, J.; Bao, Z. Side chain engineering in solution-processable conjugated polymers. Chem. Mater. 2014, 26, 604-615.
    • (2014) Chem. Mater. , vol.26 , pp. 604-615
    • Mei, J.1    Bao, Z.2
  • 34
    • 67749101411 scopus 로고    scopus 로고
    • Development of new semiconducting polymers for high performance solar cells
    • Liang, Y.; Wu, Y.; Feng, D.; Tsai, S.T.; Son, H.J.; Li, G.; Yu, L. Development of new semiconducting polymers for high performance solar cells. J. Am. Chem. Soc. 2008, 131, 56-57.
    • (2008) J. Am. Chem. Soc. , vol.131 , pp. 56-57
    • Liang, Y.1    Wu, Y.2    Feng, D.3    Tsai, S.T.4    Son, H.J.5    Li, G.6    Yu, L.7
  • 35
    • 77951907456 scopus 로고    scopus 로고
    • For the bright future-Bulk heterojunction polymer solar cells with power conversion efficiency of 7.4%
    • Liang, Y.; Xu, Z.; Xia, J.; Tsai, S.T.; Wu, Y.; Li, G.; Ray, C.; Yu, L. For the bright future-Bulk heterojunction polymer solar cells with power conversion efficiency of 7.4%. Adv. Mater. 2010, 22, E135-E138.
    • (2010) Adv. Mater. , vol.22
    • Liang, Y.1    Xu, Z.2    Xia, J.3    Tsai, S.T.4    Wu, Y.5    Li, G.6    Ray, C.7    Yu, L.8
  • 36
    • 51549089043 scopus 로고    scopus 로고
    • Bandgap and molecular energy level control of conjugated polymer photovoltaic materials based on benzo[1,2-b:4, 5-b']dithiophene
    • Hou, J.; Park, M.H.; Zhang, S.; Yao, Y.; Chen, L.M.; Li, J.H.; Yang, Y. Bandgap and molecular energy level control of conjugated polymer photovoltaic materials based on benzo[1,2-b:4, 5-b']dithiophene. Macromolecules 2008, 41, 6012-6018.
    • (2008) Macromolecules , vol.41 , pp. 6012-6018
    • Hou, J.1    Park, M.H.2    Zhang, S.3    Yao, Y.4    Chen, L.M.5    Li, J.H.6    Yang, Y.7
  • 37
    • 0028375885 scopus 로고
    • A study of the electrochemical properties of conducting polymers for application in electrochemical capacitors
    • Rudge, A.; Raistrick, I.; Gottesfeld, S.; Ferraris, J.P. A study of the electrochemical properties of conducting polymers for application in electrochemical capacitors. Electrochim. Acta 1994, 39, 273-287.
    • (1994) Electrochim. Acta , vol.39 , pp. 273-287
    • Rudge, A.1    Raistrick, I.2    Gottesfeld, S.3    Ferraris, J.P.4
  • 39
    • 0022962075 scopus 로고
    • Field-effect transistor with polythiophene thin film
    • Koezuka, H.; Tsumura, A.; Ando, T. Field-effect transistor with polythiophene thin film. Synt. Met. 1987, 18, 699-704.
    • (1987) Synt. Met. , vol.18 , pp. 699-704
    • Koezuka, H.1    Tsumura, A.2    Ando, T.3
  • 40
    • 37049072469 scopus 로고
    • Enhanced electrical conductivity in regioselectively synthesized poly (3-alkylthiophenes)
    • McCullough, R.D.; Lowe, R.D. Enhanced electrical conductivity in regioselectively synthesized poly (3-alkylthiophenes). J. Chem. Soc. Chem. Commun. 1992, 1, 70-72.
    • (1992) J. Chem. Soc. Chem. Commun. , vol.1 , pp. 70-72
    • McCullough, R.D.1    Lowe, R.D.2
  • 41
    • 84923157083 scopus 로고
    • The first regioregular head-to-tail poly(3-hexylthiophene-2,5-diyl) and a regiorandom isopolymer: Nickel vs. palladium catalysis of 2(5)-bromo-5(2)-(bromozincio)-3-hexylthiophene polymerization
    • Chen, T.A.; Rieke, R.D. The first regioregular head-to-tail poly(3-hexylthiophene-2,5-diyl) and a regiorandom isopolymer: Nickel vs. palladium catalysis of 2(5)-bromo-5(2)-(bromozincio)-3-hexylthiophene polymerization. J. Am. Chem. Soc. 1992, 114, 10087-10088.
    • (1992) J. Am. Chem. Soc , vol.114 , pp. 10087-10088
    • Chen, T.A.1    Rieke, R.D.2
  • 42
    • 0033077140 scopus 로고    scopus 로고
    • A simple method to prepare head-to-tail coupled, regioregular poly(3-alkylthiophenes) using grignard metathesis
    • Loewe, R.S.; Khersonsky, S.M.; McCullough, R.D. A simple method to prepare head-to-tail coupled, regioregular poly(3-alkylthiophenes) using grignard metathesis. Adv. Mater. 1999, 11, 250-253.
    • (1999) Adv. Mater. , vol.11 , pp. 250-253
    • Loewe, R.S.1    Khersonsky, S.M.2    McCullough, R.D.3
  • 43
  • 44
    • 33644634092 scopus 로고    scopus 로고
    • High-efficiency solution processable polymer photovoltaic cells by self-organization of polymer blends
    • Li, G.; Shrotriya, V.; Huang, J.; Yao, Y.; Moriarty, T.; Emery, K.; Yang, Y. High-efficiency solution processable polymer photovoltaic cells by self-organization of polymer blends. Nat. Mater. 2005, 4, 864-868.
    • (2005) Nat. Mater. , vol.4 , pp. 864-868
    • Li, G.1    Shrotriya, V.2    Huang, J.3    Yao, Y.4    Moriarty, T.5    Emery, K.6    Yang, Y.7
  • 45
    • 26844438506 scopus 로고    scopus 로고
    • Thermally stable, efficient polymer solar cells with nanoscale control of the interpenetrating network morphology
    • Ma, W.; Yang, C.; Gong, X.; Lee, K.; Heeger, A.J. Thermally stable, efficient polymer solar cells with nanoscale control of the interpenetrating network morphology. Adv. Func. Mater. 2005, 15, 1617-1622.
    • (2005) Adv. Func. Mater. , vol.15 , pp. 1617-1622
    • Ma, W.1    Yang, C.2    Gong, X.3    Lee, K.4    Heeger, A.J.5
  • 46
    • 33644647169 scopus 로고    scopus 로고
    • Morphology of polymer/fullerene bulk heterojunction solar cells
    • Hoppe, H.; Sariciftci, N.S. Morphology of polymer/fullerene bulk heterojunction solar cells. J. Mater. Chem. 2006, 16, 45-61.
    • (2006) J. Mater. Chem. , vol.16 , pp. 45-61
    • Hoppe, H.1    Sariciftci, N.S.2
  • 50
    • 33947091124 scopus 로고
    • Selective carbon-carbon bond formation by cross-coupling of grignard reagents with organic halides Catalysis by nickel-phosphine complexes
    • Tamao, K.; Sumitani, K.; Kumada, M. Selective carbon-carbon bond formation by cross-coupling of grignard reagents with organic halides. Catalysis by nickel-phosphine complexes. J. Am. Chem. Soc. 1972, 94, 4374-4376.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 4374-4376
    • Tamao, K.1    Sumitani, K.2    Kumada, M.3
  • 51
    • 84985570392 scopus 로고
    • The palladium-catalyzed cross-coupling reactions of organotin reagents with organic electrophiles [New Synthetic Methods (58)]
    • Stille, J.K. The palladium-catalyzed cross-coupling reactions of organotin reagents with organic electrophiles [New Synthetic Methods (58)]. Angew. Chem. Int. Ed. 1986, 25, 508-524.
    • (1986) Angew. Chem. Int. Ed. , vol.25 , pp. 508-524
    • Stille, J.K.1
  • 52
    • 2042507954 scopus 로고
    • Palladium-catalyzed cross-coupling reactions of organoboron compounds
    • Miyaura, N.; Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 1995, 95, 2457-5483.
    • (1995) Chem. Rev. , vol.95 , pp. 2457-5483
    • Miyaura, N.1    Suzuki, A.2
  • 53
    • 84981761646 scopus 로고
    • über triphenyl-phosphinmethylene als olefinbildende reagenzien (II. Mitteil.1)
    • (in German)
    • Wittig, G.; Haag, W. über triphenyl-phosphinmethylene als olefinbildende reagenzien (II. Mitteil.1). Chem. Ber. 1955, 88, 1654-1666. (in German)
    • (1955) Chem. Ber , vol.88 , pp. 1654-1666
    • Wittig, G.1    Haag, W.2
  • 54
    • 77956602917 scopus 로고
    • Phosphororganische verbindungen, XX. Phosphinoxyde als olefinierungsreagenzien
    • (in German)
    • Horner, L.; Hoffmann, H.; Wippel, H.G.; Klahre, G. Phosphororganische verbindungen, XX. Phosphinoxyde als olefinierungsreagenzien. Chem. Ber. 1959, 92, 2499-2505. (in German)
    • (1959) Chem. Ber. , vol.92 , pp. 2499-2505
    • Horner, L.1    Hoffmann, H.2    Wippel, H.G.3    Klahre, G.4
  • 55
    • 77956606957 scopus 로고
    • Phosphororganische verbindungen, XII. Phosphinoxyde als olefinierungsreagenzien
    • (in German)
    • Horner, L.; Hoffmann, H.; Wippel, H.G. Phosphororganische verbindungen, XII. Phosphinoxyde als olefinierungsreagenzien. Chem. Ber. 1958, 91, 61-63. (in German)
    • (1958) Chem. Ber , vol.91 , pp. 61-63
    • Horner, L.1    Hoffmann, H.2    Wippel, H.G.3
  • 56
    • 84981750119 scopus 로고
    • Condensation von malonsäure mit aromatischen aldehyden durch ammoniak und amine. Ber. Dtsch
    • (in German)
    • Knoevenagel, E. Condensation von malonsäure mit aromatischen aldehyden durch ammoniak und amine. Ber. Dtsch. Chem. Ges. 1898, 31, 2596-2619. (in German)
    • (1898) Chem. Ges , vol.31 , pp. 2596-2619
    • Knoevenagel, E.1
  • 57
    • 33645896595 scopus 로고
    • Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides
    • Heck, R.; Nolley, J., Jr. Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides. J. Org. Chem. 1972, 37, 2320-2322.
    • (1972) J. Org. Chem. , vol.37 , pp. 2320-2322
    • Heck, R.1    Nolley Jr., J.2
  • 58
    • 0036643463 scopus 로고    scopus 로고
    • Development of Pd-Cu catalyzed cross-coupling of terminal acetylenes with sp2-carbon halides
    • Sonogashira, K. Development of Pd-Cu catalyzed cross-coupling of terminal acetylenes with sp2-carbon halides. J. Organomet. Chem. 2002, 653, 46-49.
    • (2002) J. Organomet. Chem. , vol.653 , pp. 46-49
    • Sonogashira, K.1
  • 59
    • 33646020399 scopus 로고    scopus 로고
    • Synthesis and photovoltaic properties of two-dimensional conjugated polythiophenes with bi(thienylenevinylene) side chains
    • Hou, J.; Tan, Z.A.; Yan, Y.; He, Y.; Yang, C.; Li, Y. Synthesis and photovoltaic properties of two-dimensional conjugated polythiophenes with bi(thienylenevinylene) side chains. J. Am. Chem. Soc. 2006, 128, 4911-4916.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 4911-4916
    • Hou, J.1    Tan, Z.A.2    Yan, Y.3    He, Y.4    Yang, C.5    Li, Y.6
  • 60
    • 33947636550 scopus 로고    scopus 로고
    • Synthesis, hole mobility, and photovoltaic properties of cross-linked polythiophenes with vinylene-terthiophene-vinylene as conjugated bridge
    • Zhou, E.; Tan, Z.A.; Yang, Y.; Huo, L.; Zou, Y.; Yang, C.; Li, Y. Synthesis, hole mobility, and photovoltaic properties of cross-linked polythiophenes with vinylene-terthiophene-vinylene as conjugated bridge. Macromolecules 2007, 40, 1831-1837.
    • (2007) Macromolecules , vol.40 , pp. 1831-1837
    • Zhou, E.1    Tan, Z.A.2    Yang, Y.3    Huo, L.4    Zou, Y.5    Yang, C.6    Li, Y.7
  • 63
    • 62549148574 scopus 로고    scopus 로고
    • Two-dimensional regioregular polythiophenes with conjugated side chains for use in organic solar cells
    • Yu, C.Y.; Ko, B.T.; Ting, C.; Chen, C.P. Two-dimensional regioregular polythiophenes with conjugated side chains for use in organic solar cells. Sol. Energy Mater. Sol. Cells 2009, 93, 613-620.
    • (2009) Sol. Energy Mater. Sol. Cells , vol.93 , pp. 613-620
    • Yu, C.Y.1    Ko, B.T.2    Ting, C.3    Chen, C.P.4
  • 64
    • 0001552029 scopus 로고
    • Synthesis of liquid-crystalline polyacrylates with laterally substituted mesogens
    • Zhou, Q.F.; Li, H.M.; Feng, X.D. Synthesis of liquid-crystalline polyacrylates with laterally substituted mesogens. Macromolecules 1987, 20, 233-234.
    • (1987) Macromolecules , vol.20 , pp. 233-234
    • Zhou, Q.F.1    Li, H.M.2    Feng, X.D.3
  • 65
    • 57349156831 scopus 로고    scopus 로고
    • Synthesis, photophysics, and electroluminescence of copolyfluorenes containing jacketed and silyl units
    • Wang, P.; Yang, Q.; Jin, H.; Liu, W.; Shen, Z.; Chen, X.; Fan, X.; Zou, D.; Zhou, Q. Synthesis, photophysics, and electroluminescence of copolyfluorenes containing jacketed and silyl units. Macromolecules 2008, 41, 8354-8359.
    • (2008) Macromolecules , vol.41 , pp. 8354-8359
    • Wang, P.1    Yang, Q.2    Jin, H.3    Liu, W.4    Shen, Z.5    Chen, X.6    Fan, X.7    Zou, D.8    Zhou, Q.9
  • 66
    • 84881580899 scopus 로고    scopus 로고
    • Effect of side-chain architecture on the optical and crystalline properties of two-dimensional polythiophenes
    • Kuo, C.Y.; Huang, Y.C.; Hsiow, C.Y.; Yang, Y.W.; Huang, C.I.; Rwei, S.P.; Wang, H.L.; Wang, L. Effect of side-chain architecture on the optical and crystalline properties of two-dimensional polythiophenes. Macromolecules 2013, 46, 5985-5997.
    • (2013) Macromolecules , vol.46 , pp. 5985-5997
    • Kuo, C.Y.1    Huang, Y.C.2    Hsiow, C.Y.3    Yang, Y.W.4    Huang, C.I.5    Rwei, S.P.6    Wang, H.L.7    Wang, L.8
  • 67
    • 33644945010 scopus 로고    scopus 로고
    • Triphenylamine-thienylenevinylene hybrid systems with internal charge transfer as donor materials for heterojunction solar cells
    • Roquet, S.; Cravino, A.; Leriche, P.; Alévêque, O.; Frère, P.; Roncali, J. Triphenylamine-thienylenevinylene hybrid systems with internal charge transfer as donor materials for heterojunction solar cells. J. Am. Chem. Soc. 2006, 128, 3459-3466.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 3459-3466
    • Roquet, S.1    Cravino, A.2    Leriche, P.3    Alévêque, O.4    Frère, P.5    Roncali, J.6
  • 68
    • 0028509008 scopus 로고
    • Thermally stable multilared organic electroluminescent devices using novel starburst molecules, 4,4',4''-Tri(N-carbazolyl) triphenylamine (TCTA) and 4,4',4''-Tris (3-methylphenylphenylamino) triphenylamine (m-MTDATA), as hole-transport materials
    • Kuwabara, Y.; Ogawa, H.; Inada, H.; Noma, N.; Shirota, Y. Thermally stable multilared organic electroluminescent devices using novel starburst molecules, 4,4',4''-Tri(N-carbazolyl) triphenylamine (TCTA) and 4,4',4''-Tris (3-methylphenylphenylamino) triphenylamine (m-MTDATA), as hole-transport materials. Adv. Mater. 1994, 6, 677-679.
    • (1994) Adv. Mater. , vol.6 , pp. 677-679
    • Kuwabara, Y.1    Ogawa, H.2    Inada, H.3    Noma, N.4    Shirota, Y.5
  • 69
    • 45449102136 scopus 로고    scopus 로고
    • Synthesis and properties of polythiophene derivatives containing triphenylamine moiety and their photovoltaic applications
    • Li, Y.; Xue, L.; Xia, H.; Xu, B.; Wen, S.; Tian, W. Synthesis and properties of polythiophene derivatives containing triphenylamine moiety and their photovoltaic applications. J. Polym. Sci. A Polym. Chem. 2008, 46, 3970-3984.
    • (2008) J. Polym. Sci. A Polym. Chem. , vol.46 , pp. 3970-3984
    • Li, Y.1    Xue, L.2    Xia, H.3    Xu, B.4    Wen, S.5    Tian, W.6
  • 70
    • 78651392871 scopus 로고    scopus 로고
    • Bulky side-chain density effect on the photophysical, electrochemical and photovoltaic properties of polythiophene derivatives
    • Wang, H.J.; Chan, L.H.; Chen, C.P.; Lin, S.L.; Lee, R.H.; Jeng, R.J. Bulky side-chain density effect on the photophysical, electrochemical and photovoltaic properties of polythiophene derivatives. Polymer 2011, 52, 326-338.
    • (2011) Polymer , vol.52 , pp. 326-338
    • Wang, H.J.1    Chan, L.H.2    Chen, C.P.3    Lin, S.L.4    Lee, R.H.5    Jeng, R.J.6
  • 71
    • 84862907456 scopus 로고    scopus 로고
    • Conjugated side-chain isolated polythiophene: Synthesis and photovoltaic application
    • Zhang, Z.G.; Zhang, S.; Min, J.; Chui, C.; Zhang, J.; Zhang, M.; Li, Y. Conjugated side-chain isolated polythiophene: Synthesis and photovoltaic application. Macromolecules 2011, 45, 113-118.
    • (2011) Macromolecules , vol.45 , pp. 113-118
    • Zhang, Z.G.1    Zhang, S.2    Min, J.3    Chui, C.4    Zhang, J.5    Zhang, M.6    Li, Y.7
  • 72
    • 84865234706 scopus 로고    scopus 로고
    • Synthesis and photovoltaic properties of two-dimensional conjugated polythiophene derivatives presenting conjugated triphenylamine/thiophene moieties
    • Wang, H.J.; Chen, Y.P.; Chen, Y.C.; Chen, C.P.; Lee, R.H.; Chan, L.H.; Jeng, R.J. Synthesis and photovoltaic properties of two-dimensional conjugated polythiophene derivatives presenting conjugated triphenylamine/thiophene moieties. Polymer 2012, 53, 4091-4103.
    • (2012) Polymer , vol.53 , pp. 4091-4103
    • Wang, H.J.1    Chen, Y.P.2    Chen, Y.C.3    Chen, C.P.4    Lee, R.H.5    Chan, L.H.6    Jeng, R.J.7
  • 75
    • 79957658883 scopus 로고    scopus 로고
    • Polythiophene derivative comprising carbazoles as pendant groups for polymer solar cell applications
    • Wang, H.J.; Chan, L.H.; Chen, C.P.; Lee, R.H.; Su, W.C.; Jeng, R.J. Polythiophene derivative comprising carbazoles as pendant groups for polymer solar cell applications. Thin Solid Films 2011, 519, 5264-5269.
    • (2011) Thin Solid Films , vol.519 , pp. 5264-5269
    • Wang, H.J.1    Chan, L.H.2    Chen, C.P.3    Lee, R.H.4    Su, W.C.5    Jeng, R.J.6
  • 76
    • 84872106496 scopus 로고    scopus 로고
    • Novel polythiophene derivatives functionalized with conjugated side-chain pendants comprising triphenylamine/carbazole moieties for photovoltaic cell applications
    • Wang, H.J.; Tzeng, J.Y.; Chou, C.W.; Huang, C.Y.; Lee, R.H.; Jeng, R.J. Novel polythiophene derivatives functionalized with conjugated side-chain pendants comprising triphenylamine/carbazole moieties for photovoltaic cell applications. Polym. Chem. 2013, 4, 506-519.
    • (2013) Polym. Chem. , vol.4 , pp. 506-519
    • Wang, H.J.1    Tzeng, J.Y.2    Chou, C.W.3    Huang, C.Y.4    Lee, R.H.5    Jeng, R.J.6
  • 77
    • 34547499651 scopus 로고    scopus 로고
    • Synthesis of a soluble n-type cyano substituted polythiophene derivative: A potential electron acceptor in polymeric solar cells
    • Chochos, C.L.; Economopoulos, S.P.; Deimede, V.; Gregoriou, V.G.; Lloyd, M.T.; Malliaras, G.G.; Kallitsis, J.K. Synthesis of a soluble n-type cyano substituted polythiophene derivative: A potential electron acceptor in polymeric solar cells. J. Phys. Chem. C 2007, 111, 10732-10740.
    • (2007) J. Phys. Chem. C , vol.111 , pp. 10732-10740
    • Chochos, C.L.1    Economopoulos, S.P.2    Deimede, V.3    Gregoriou, V.G.4    Lloyd, M.T.5    Malliaras, G.G.6    Kallitsis, J.K.7
  • 78
    • 50949094881 scopus 로고    scopus 로고
    • Intramolecular donor-acceptor regioregular poly (3-hexylthiophene)s presenting octylphenanthrenyl-imidazole moieties exhibit enhanced charge transfer for heterojunction solar cell applications
    • Chang, Y.T.; Hsu, S.L.; Chen, G.Y.; Su, M.H.; Singh, T.A.; Diau, E.W.G.; Wei, K.H. Intramolecular donor-acceptor regioregular poly (3-hexylthiophene)s presenting octylphenanthrenyl-imidazole moieties exhibit enhanced charge transfer for heterojunction solar cell applications. Adv. Func. Mater. 2008, 18, 2356-2365.
    • (2008) Adv. Func. Mater. , vol.18 , pp. 2356-2365
    • Chang, Y.T.1    Hsu, S.L.2    Chen, G.Y.3    Su, M.H.4    Singh, T.A.5    Diau, E.W.G.6    Wei, K.H.7
  • 79
    • 84880439938 scopus 로고    scopus 로고
    • Polythiophenes comprising conjugated pendants toward long-term air-stable inverted polymer solar cells with high open circuit voltages
    • Wang, H.J.; Chou, C.W.; Chen, C.P.; Chen, Y.H.; Lee, R.H.; Jeng, R.J. Polythiophenes comprising conjugated pendants toward long-term air-stable inverted polymer solar cells with high open circuit voltages. J. Mater. Chem. A 2013, 1, 8950-8960.
    • (2013) J. Mater. Chem. A , vol.1 , pp. 8950-8960
    • Wang, H.J.1    Chou, C.W.2    Chen, C.P.3    Chen, Y.H.4    Lee, R.H.5    Jeng, R.J.6
  • 80
    • 84873958031 scopus 로고    scopus 로고
    • 3-Fluoro-4-hexylthiophene as a building block for tuning the electronic properties of conjugated polythiophenes
    • Gohier, F.; Frère, P.; Roncali, J. 3-Fluoro-4-hexylthiophene as a building block for tuning the electronic properties of conjugated polythiophenes. J. Org. Chem. 2013, 78, 1497-1503.
    • (2013) J. Org. Chem. , vol.78 , pp. 1497-1503
    • Gohier, F.1    Frère, P.2    Roncali, J.3
  • 81
    • 67650555653 scopus 로고    scopus 로고
    • Highly efficient solar cell polymers developed via fine-tuning of structural and electronic properties
    • Liang, Y.; Feng, D.; Wu, Y.; Tsai, S.T.; Li, G.; Ray, C.; Yu, L. Highly efficient solar cell polymers developed via fine-tuning of structural and electronic properties. J. Am. Chem. Soc. 2009, 131, 7792-7799.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 7792-7799
    • Liang, Y.1    Feng, D.2    Wu, Y.3    Tsai, S.T.4    Li, G.5    Ray, C.6    Yu, L.7
  • 83
    • 77956948185 scopus 로고    scopus 로고
    • A new class of semiconducting polymers for bulk heterojunction solar cells with exceptionally high performance
    • Liang, Y.; Yu, L. A new class of semiconducting polymers for bulk heterojunction solar cells with exceptionally high performance. Acc. Chem. Res. 2009, 43, 1227-1236.
    • (2009) Acc. Chem. Res. , vol.43 , pp. 1227-1236
    • Liang, Y.1    Yu, L.2
  • 84
    • 76649101420 scopus 로고    scopus 로고
    • A polybenzo [1,2-b:4,5-b'] dithiophene derivative with deep HOMO level and its application in high-performance polymer solar cells
    • Huo, L.; Hou, J.; Zhang, S.; Chen, H.Y.; Yang, Y. A polybenzo [1,2-b:4,5-b'] dithiophene derivative with deep HOMO level and its application in high-performance polymer solar cells. Angew. Chem. Int. Ed. 2010, 49, 1500-1503.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 1500-1503
    • Huo, L.1    Hou, J.2    Zhang, S.3    Chen, H.Y.4    Yang, Y.5
  • 85
    • 79960957433 scopus 로고    scopus 로고
    • Synthesis of a polythieno [3, 4-b] thiophene derivative with a low-lying HOMO level and its application in polymer solar cells
    • Huo, L.; Guo, X.; Li, Y.; Hou, J. Synthesis of a polythieno [3, 4-b] thiophene derivative with a low-lying HOMO level and its application in polymer solar cells. Chem. Commun. 2011, 47, 8850-8852.
    • (2011) Chem. Commun. , vol.47 , pp. 8850-8852
    • Huo, L.1    Guo, X.2    Li, Y.3    Hou, J.4
  • 86
    • 84859572373 scopus 로고    scopus 로고
    • Replacing alkoxy groups with alkylthienyl groups: A feasible approach to improve the properties of photovoltaic polymers
    • Huo, L.; Zhang, S.; Guo, X.; Xu, F.; Li, Y.; Hou, J. Replacing alkoxy groups with alkylthienyl groups: A feasible approach to improve the properties of photovoltaic polymers. Angew. Chem. Int. Ed. 2011, 123, 9871-9876.
    • (2011) Angew. Chem. Int. Ed. , vol.123 , pp. 9871-9876
    • Huo, L.1    Zhang, S.2    Guo, X.3    Xu, F.4    Li, Y.5    Hou, J.6
  • 87
    • 82955193891 scopus 로고    scopus 로고
    • A copolymer of benzodithiophene with TIPS side chains for enhanced photovoltaic performance
    • Shi, Q.; Fan, H.; Liu, Y.; Hu, W.; Li, Y.; Zhan, X. A copolymer of benzodithiophene with TIPS side chains for enhanced photovoltaic performance. Macromolecules 2011, 44, 9173-9179.
    • (2011) Macromolecules , vol.44 , pp. 9173-9179
    • Shi, Q.1    Fan, H.2    Liu, Y.3    Hu, W.4    Li, Y.5    Zhan, X.6
  • 88
    • 84875842886 scopus 로고    scopus 로고
    • Synthesis and photovoltaic properties of two-dimension-conjugated D-A copolymers based on benzodithiophene or benzodifuran units
    • Zhang, Y.; Gao, L.; He, C.; Sun, Q.; Li, Y. Synthesis and photovoltaic properties of two-dimension-conjugated D-A copolymers based on benzodithiophene or benzodifuran units. Polym. Chem. 2013, 4, 1474-1481.
    • (2013) Polym. Chem. , vol.4 , pp. 1474-1481
    • Zhang, Y.1    Gao, L.2    He, C.3    Sun, Q.4    Li, Y.5
  • 89
    • 79951546202 scopus 로고    scopus 로고
    • Synthesis of fluorinated polythienothiophene-co-benzodithiophenes and effect of fluorination on the photovoltaic properties
    • Son, H.J.; Wang, W.; Xu, T.; Liang, Y.; Wu, Y.; Li, G.; Yu, L. Synthesis of fluorinated polythienothiophene-co-benzodithiophenes and effect of fluorination on the photovoltaic properties. J. Am. Chem. Soc. 2011, 133, 1885-1894.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 1885-1894
    • Son, H.J.1    Wang, W.2    Xu, T.3    Liang, Y.4    Wu, Y.5    Li, G.6    Yu, L.7
  • 90
    • 79952632715 scopus 로고    scopus 로고
    • Development of fluorinated benzothiadiazole as a structural unit for a polymer solar cell of 7% efficiency
    • Zhou, H.; Yang, L.; Stuart, A.C.; Price, S.C.; Liu, S.; You, W. Development of fluorinated benzothiadiazole as a structural unit for a polymer solar cell of 7% efficiency. Angew. Chem. Int. Ed. 2011, 50, 2995-2998.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 2995-2998
    • Zhou, H.1    Yang, L.2    Stuart, A.C.3    Price, S.C.4    Liu, S.5    You, W.6
  • 91
    • 79953054021 scopus 로고    scopus 로고
    • Fluorine substituted conjugated polymer of medium band gap yields 7% efficiency in polymer-fullerene solar cells
    • Price, S.C.; Stuart, A.C.; Yang, L.; Zhou, H.; You, W. Fluorine substituted conjugated polymer of medium band gap yields 7% efficiency in polymer-fullerene solar cells. J. Am. Chem. Soc. 2011, 133, 4625-4631.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 4625-4631
    • Price, S.C.1    Stuart, A.C.2    Yang, L.3    Zhou, H.4    You, W.5
  • 92
    • 52449092820 scopus 로고    scopus 로고
    • Low-bandgap poly(thiophene-phenylene-thiophene) derivatives with broaden absorption spectra for use in high-performance bulk-heterojunction polymer solar cells
    • Chen, C.P.; Chan, S.H.; Chao, T.C.; Ting, C.; Ko, B.T. Low-bandgap poly(thiophene-phenylene-thiophene) derivatives with broaden absorption spectra for use in high-performance bulk-heterojunction polymer solar cells. J. Am. Chem. Soc. 2008, 130, 12828-12833.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 12828-12833
    • Chen, C.P.1    Chan, S.H.2    Chao, T.C.3    Ting, C.4    Ko, B.T.5
  • 93
    • 79955650512 scopus 로고    scopus 로고
    • Indacenodithiophene and quinoxaline-based conjugated polymers for highly efficient polymer solar cells
    • Zhang, Y.; Zou, J.; Yip, H.L.; Chen, K.S.; Zeigler, D.F.; Sun, Y.; Jen, A.K.Y. Indacenodithiophene and quinoxaline-based conjugated polymers for highly efficient polymer solar cells. Chem. Mater. 2011, 23, 2289-2291.
    • (2011) Chem. Mater. , vol.23 , pp. 2289-2291
    • Zhang, Y.1    Zou, J.2    Yip, H.L.3    Chen, K.S.4    Zeigler, D.F.5    Sun, Y.6    Jen, A.K.Y.7
  • 94
    • 80052986200 scopus 로고    scopus 로고
    • Synthesis and photovoltaic properties of D-A copolymers based on alkyl-substituted indacenodithiophene donor unit
    • Zhang, M.; Guo, X.; Wang, X.; Wang, H.; Li, Y. Synthesis and photovoltaic properties of D-A copolymers based on alkyl-substituted indacenodithiophene donor unit. Chem. Mater. 2011, 23, 4264-4270.
    • (2011) Chem. Mater. , vol.23 , pp. 4264-4270
    • Zhang, M.1    Guo, X.2    Wang, X.3    Wang, H.4    Li, Y.5
  • 95
    • 77956038241 scopus 로고    scopus 로고
    • Low-bandgap conjugated polymer for high efficient photovoltaic applications
    • Chen, Y.C.; Yu, C.Y.; Fan, Y.L.; Hung, L.I.; Chen, C.P.; Ting, C. Low-bandgap conjugated polymer for high efficient photovoltaic applications. Chem. Commun. 2010, 46, 6503-6505.
    • (2010) Chem. Commun. , vol.46 , pp. 6503-6505
    • Chen, Y.C.1    Yu, C.Y.2    Fan, Y.L.3    Hung, L.I.4    Chen, C.P.5    Ting, C.6
  • 96
    • 84872714821 scopus 로고    scopus 로고
    • Increased open circuit voltage in a fluorinated quinoxaline-based alternating conjugated polymer
    • Chen, C.P.; Chen, Y.C.; Yu, C.Y. Increased open circuit voltage in a fluorinated quinoxaline-based alternating conjugated polymer. Polym. Chem. 2013, 4, 1161-1166.
    • (2013) Polym. Chem. , vol.4 , pp. 1161-1166
    • Chen, C.P.1    Chen, Y.C.2    Yu, C.Y.3
  • 97
    • 84885631179 scopus 로고    scopus 로고
    • Increasing the open-circuit voltage in high-performance organic photovoltaic devices through conformational twisting of an indacenodithiophene-based conjugated polymer
    • Chen, C.P.; Hsu, H.L. Increasing the open-circuit voltage in high-performance organic photovoltaic devices through conformational twisting of an indacenodithiophene-based conjugated polymer. Macromol. Rapid Commun. 2013, 34, 1623-1628.
    • (2013) Macromol. Rapid Commun. , vol.34 , pp. 1623-1628
    • Chen, C.P.1    Hsu, H.L.2


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