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Volumn 105, Issue , 2014, Pages 192-201

The master factors influencing the efficiency of D-A-π-A configurated organic sensitizers in dye-sensitized solar cell via theoretically characterization: Design and verification

Author keywords

Auxiliary acceptor; D A A dyes; Density functional theory; Dye sensitized solar cells; Quinoxaline based dye; Time dependent density functional theory

Indexed keywords

AUXILIARY ACCEPTOR; DYE-SENSITIZED SOLAR CELL; DYE-SENSITIZED SOLAR CELLS; EXCITON-BINDING ENERGY; LIGHT HARVESTING PROPERTIES; TIME DEPENDENT DENSITY FUNCTIONAL THEORY; TOTAL REORGANIZATION ENERGY; VERTICAL DIPOLE MOMENTS;

EID: 84896864622     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2014.01.030     Document Type: Article
Times cited : (26)

References (60)
  • 3
    • 66749163106 scopus 로고    scopus 로고
    • Molecular designs and syntheses of organic dyes for dye-sensitized solar cells
    • Y. Ooyama, and Y. Harima Molecular designs and syntheses of organic dyes for dye-sensitized solar cells Eur J Org Chem 2009 2009 2903 2934
    • (2009) Eur J Org Chem , vol.2009 , pp. 2903-2934
    • Ooyama, Y.1    Harima, Y.2
  • 4
    • 0038462260 scopus 로고    scopus 로고
    • Molecular photovoltaics
    • A. Hagfeldt, and M. Grätzel Molecular photovoltaics Acc Chem Res 33 2000 269 277
    • (2000) Acc Chem Res , vol.33 , pp. 269-277
    • Hagfeldt, A.1    Grätzel, M.2
  • 5
    • 0035891138 scopus 로고    scopus 로고
    • Photoelectrochemical cells
    • M. Grätzel Photoelectrochemical cells Nature 414 2001 338 344
    • (2001) Nature , vol.414 , pp. 338-344
    • Grätzel, M.1
  • 6
    • 34249784386 scopus 로고    scopus 로고
    • A high light-harvesting-efficiency coumarin dye for stable dye-sensitized solar cells
    • Z.-S. Wang, Y. Cui, K. Hara, Y. Dan-oh, C. Kasada, and A. Shinpo A high light-harvesting-efficiency coumarin dye for stable dye-sensitized solar cells Adv Mater 19 2007 1138 1141
    • (2007) Adv Mater , vol.19 , pp. 1138-1141
    • Wang, Z.-S.1    Cui, Y.2    Hara, K.3    Dan-Oh, Y.4    Kasada, C.5    Shinpo, A.6
  • 7
    • 77951916953 scopus 로고    scopus 로고
    • Kinetic competition in a coumarin dye-sensitized solar cell: Injection and recombination limitations upon device performance
    • S.E. Koops, P.R.F. Barnes, B.C. O'Regan, and J.R. Durrant Kinetic competition in a coumarin dye-sensitized solar cell: injection and recombination limitations upon device performance J Phys Chem C 114 2010 8054 8061
    • (2010) J Phys Chem C , vol.114 , pp. 8054-8061
    • Koops, S.E.1    Barnes, P.R.F.2    O'Regan, B.C.3    Durrant, J.R.4
  • 8
    • 73949113829 scopus 로고    scopus 로고
    • Organic dyes incorporating the dithieno[3,2-b:2′,3′-d] thiophene moiety for efficient dye-sensitized solar cells
    • H.-Y. Yang, Y.-S. Yen, Y.-C. Hsu, H.-H. Chou, and J.-T. Lin Organic dyes incorporating the dithieno[3,2-b:2′,3′-d]thiophene moiety for efficient dye-sensitized solar cells Org Lett 12 2009 16 19
    • (2009) Org Lett , vol.12 , pp. 16-19
    • Yang, H.-Y.1    Yen, Y.-S.2    Hsu, Y.-C.3    Chou, H.-H.4    Lin, J.-T.5
  • 9
    • 79960867973 scopus 로고    scopus 로고
    • Engineering organic sensitizers for iodine-free dye-sensitized solar cells: Red-shifted current response concomitant with attenuated charge recombination
    • Y. Bai, J. Zhang, D. Zhou, Y. Wang, M. Zhang, and P. Wang Engineering organic sensitizers for iodine-free dye-sensitized solar cells: red-shifted current response concomitant with attenuated charge recombination J Am Chem Soc 133 2011 11442 11445
    • (2011) J Am Chem Soc , vol.133 , pp. 11442-11445
    • Bai, Y.1    Zhang, J.2    Zhou, D.3    Wang, Y.4    Zhang, M.5    Wang, P.6
  • 10
    • 47649088268 scopus 로고    scopus 로고
    • Organic dye-sensitized ionic liquid based solar cells: Remarkable enhancement in performance through molecular design of indoline sensitizers
    • D. Kuang, S. Uchida, R. Humphry-Baker, S.M. Zakeeruddin, and M. Grätzel Organic dye-sensitized ionic liquid based solar cells: remarkable enhancement in performance through molecular design of indoline sensitizers Angew Chem Int Ed Engl 47 2008 1923 1927
    • (2008) Angew Chem Int Ed Engl , vol.47 , pp. 1923-1927
    • Kuang, D.1    Uchida, S.2    Humphry-Baker, R.3    Zakeeruddin, S.M.4    Grätzel, M.5
  • 11
    • 54949113737 scopus 로고    scopus 로고
    • High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye
    • S. Ito, H. Miura, S. Uchida, M. Takata, K. Sumioka, and P. Liska et al. High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye Chem Commun 2008 5194 5196
    • (2008) Chem Commun , pp. 5194-5196
    • Ito, S.1    Miura, H.2    Uchida, S.3    Takata, M.4    Sumioka, K.5    Liska, P.6
  • 12
    • 80052318280 scopus 로고    scopus 로고
    • Metal-free organic sensitizers with a sterically hindered thiophene unit for efficient dye-sensitized solar cells
    • E. Kozma, I. Concina, A. Braga, L. Borgese, L.E. Depero, and A. Vomiero et al. Metal-free organic sensitizers with a sterically hindered thiophene unit for efficient dye-sensitized solar cells J Mater Chem 21 2011 13785 13788
    • (2011) J Mater Chem , vol.21 , pp. 13785-13788
    • Kozma, E.1    Concina, I.2    Braga, A.3    Borgese, L.4    Depero, L.E.5    Vomiero, A.6
  • 13
    • 84870870175 scopus 로고    scopus 로고
    • Synthesis and applications of new triphenylamine dyes with donor-donor-(bridge)-acceptor structure for organic dye-sensitized solar cells
    • C. Sakong, H.-J. Kim, S.-H. Kim, J.-W. Namgoong, J.-H. Park, and J.-H. Ryu et al. Synthesis and applications of new triphenylamine dyes with donor-donor-(bridge)-acceptor structure for organic dye-sensitized solar cells New J Chem 36 2012 2025 2032
    • (2012) New J Chem , vol.36 , pp. 2025-2032
    • Sakong, C.1    Kim, H.-J.2    Kim, S.-H.3    Namgoong, J.-W.4    Park, J.-H.5    Ryu, J.-H.6
  • 14
    • 34548548752 scopus 로고    scopus 로고
    • Review of recent progress in dye-sensitized solar cells
    • F.-T. Kong, S.-Y. Dai, and K.-J. Wang Review of recent progress in dye-sensitized solar cells Adv OptoElectron 2007 2007 1 13
    • (2007) Adv OptoElectron , vol.2007 , pp. 1-13
    • Kong, F.-T.1    Dai, S.-Y.2    Wang, K.-J.3
  • 15
    • 70349784869 scopus 로고    scopus 로고
    • Metal-free organic dyes for dye-sensitized solar cells: From structure: Property relationships to design rules
    • A. Mishra, M.K. Fischer, and P. Bauerle Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationships to design rules Angew Chem Int Ed Engl 48 2009 2474 2499
    • (2009) Angew Chem Int Ed Engl , vol.48 , pp. 2474-2499
    • Mishra, A.1    Fischer, M.K.2    Bauerle, P.3
  • 16
    • 79951938063 scopus 로고    scopus 로고
    • Sensitizer molecular structure-device efficiency relationship in dye sensitized solar cells
    • J.N. Clifford, E. Martinez-Ferrero, A. Viterisi, and E. Palomares Sensitizer molecular structure-device efficiency relationship in dye sensitized solar cells Chem Soc Rev 40 2011 1635 1646
    • (2011) Chem Soc Rev , vol.40 , pp. 1635-1646
    • Clifford, J.N.1    Martinez-Ferrero, E.2    Viterisi, A.3    Palomares, E.4
  • 18
    • 84862584848 scopus 로고    scopus 로고
    • New D-π-A dyes for efficient dye-sensitized solar cells
    • S. Qu, J. Hua, and H. Tian New D-π-A dyes for efficient dye-sensitized solar cells Sci China Chem 55 2012 677 697
    • (2012) Sci China Chem , vol.55 , pp. 677-697
    • Qu, S.1    Hua, J.2    Tian, H.3
  • 19
    • 84865241564 scopus 로고    scopus 로고
    • Series of new D-A-π-A organic broadly absorbing sensitizers containing isoindigo unit for highly efficient dye-sensitized solar cells
    • W. Ying, F. Guo, J. Li, Q. Zhang, W. Wu, and H. Tian et al. Series of new D-A-π-A organic broadly absorbing sensitizers containing isoindigo unit for highly efficient dye-sensitized solar cells ACS Appl Mater Interfaces 4 2012 4215 4224
    • (2012) ACS Appl Mater Interfaces , vol.4 , pp. 4215-4224
    • Ying, W.1    Guo, F.2    Li, J.3    Zhang, Q.4    Wu, W.5    Tian, H.6
  • 20
    • 79951610276 scopus 로고    scopus 로고
    • Organic D-A-π-A solar cell sensitizers with improved stability and spectral response
    • W. Zhu, Y. Wu, S. Wang, W. Li, X. Li, and J. Chen et al. Organic D-A-π-A solar cell sensitizers with improved stability and spectral response Adv Funct Mater 21 2011 756 763
    • (2011) Adv Funct Mater , vol.21 , pp. 756-763
    • Zhu, W.1    Wu, Y.2    Wang, S.3    Li, W.4    Li, X.5    Chen, J.6
  • 21
    • 84873696574 scopus 로고    scopus 로고
    • Organic sensitizers from D-π-A to D-A-π-A: Effect of the internal electron-withdrawing units on molecular absorption, energy levels and photovoltaic performances
    • Y. Wu, and W. Zhu Organic sensitizers from D-π-A to D-A-π-A: effect of the internal electron-withdrawing units on molecular absorption, energy levels and photovoltaic performances Chem Soc Rev 42 2013 2039 2058
    • (2013) Chem Soc Rev , vol.42 , pp. 2039-2058
    • Wu, Y.1    Zhu, W.2
  • 22
    • 84862518920 scopus 로고    scopus 로고
    • Constructing organic D-A-π-A-featured sensitizers with a quinoxaline unit for high-efficiency solar cells: The effect of an auxiliary acceptor on the absorption and the energy level alignment
    • K. Pei, Y. Wu, W. Wu, Q. Zhang, B. Chen, and H. Tian et al. Constructing organic D-A-π-A-featured sensitizers with a quinoxaline unit for high-efficiency solar cells: the effect of an auxiliary acceptor on the absorption and the energy level alignment Chem Eur J 18 2012 8190 8200
    • (2012) Chem Eur J , vol.18 , pp. 8190-8200
    • Pei, K.1    Wu, Y.2    Wu, W.3    Zhang, Q.4    Chen, B.5    Tian, H.6
  • 23
    • 84883825134 scopus 로고    scopus 로고
    • Effects of the acceptors in triphenylamine-based D-A′-π-A dyes on photophysical, electrochemical, and photovoltaic properties
    • L. Wang, P. Shen, Z. Cao, X. Liu, Y. Huang, and C. Liu et al. Effects of the acceptors in triphenylamine-based D-A′-π-A dyes on photophysical, electrochemical, and photovoltaic properties J Power Sources 246 2013 831 839
    • (2013) J Power Sources , vol.246 , pp. 831-839
    • Wang, L.1    Shen, P.2    Cao, Z.3    Liu, X.4    Huang, Y.5    Liu, C.6
  • 24
    • 84877822098 scopus 로고    scopus 로고
    • D-A-π-A organic sensitizers containing a benzothiazole moiety as an additional acceptor for use in solar cells
    • J. Zeng, T. Zhang, X. Zang, D. Kuang, H. Meier, and D. Cao D-A-π-A organic sensitizers containing a benzothiazole moiety as an additional acceptor for use in solar cells Sci China Chem 56 2013 505 513
    • (2013) Sci China Chem , vol.56 , pp. 505-513
    • Zeng, J.1    Zhang, T.2    Zang, X.3    Kuang, D.4    Meier, H.5    Cao, D.6
  • 25
    • 80053523561 scopus 로고    scopus 로고
    • Incorporating benzotriazole moiety to construct D-A-π-A organic sensitizers for solar cells: Significant enhancement of open-circuit photovoltage with long alkyl group
    • Y. Cui, Y. Wu, X. Lu, X. Zhang, G. Zhou, and F.B. Miapeh et al. Incorporating benzotriazole moiety to construct D-A-π-A organic sensitizers for solar cells: significant enhancement of open-circuit photovoltage with long alkyl group Chem Mater 23 2011 4394 4401
    • (2011) Chem Mater , vol.23 , pp. 4394-4401
    • Cui, Y.1    Wu, Y.2    Lu, X.3    Zhang, X.4    Zhou, G.5    Miapeh, F.B.6
  • 26
    • 84879039387 scopus 로고    scopus 로고
    • New sensitizers bearing quinoxaline moieties as an auxiliary acceptor for dye-sensitized solar cells
    • J. Shi, Z. Chai, J. Su, J. Chen, R. Tang, and K. Fan et al. New sensitizers bearing quinoxaline moieties as an auxiliary acceptor for dye-sensitized solar cells Dye Pigment 98 2013 405 413
    • (2013) Dye Pigment , vol.98 , pp. 405-413
    • Shi, J.1    Chai, Z.2    Su, J.3    Chen, J.4    Tang, R.5    Fan, K.6
  • 27
    • 84879070259 scopus 로고    scopus 로고
    • Constructing high-efficiency D-A-π-A-featured solar cell sensitizers: A promising building block of 2,3-diphenylquinoxaline for antiaggregation and photostability
    • K. Pei, Y. Wu, A. Islam, Q. Zhang, L. Han, and H. Tian et al. Constructing high-efficiency D-A-π-A-featured solar cell sensitizers: a promising building block of 2,3-diphenylquinoxaline for antiaggregation and photostability ACS Appl Mater Interfaces 5 2013 4986 4995
    • (2013) ACS Appl Mater Interfaces , vol.5 , pp. 4986-4995
    • Pei, K.1    Wu, Y.2    Islam, A.3    Zhang, Q.4    Han, L.5    Tian, H.6
  • 28
    • 84859147773 scopus 로고    scopus 로고
    • D-A-π-A featured sensitizers bearing phthalimide and benzotriazole as auxiliary acceptor: Effect on absorption and charge recombination dynamics in dye-sensitized solar cells
    • W. Li, Y. Wu, Q. Zhang, H. Tian, and W. Zhu D-A-π-A featured sensitizers bearing phthalimide and benzotriazole as auxiliary acceptor: effect on absorption and charge recombination dynamics in dye-sensitized solar cells ACS Appl Mater Interfaces 4 2012 1822 1830
    • (2012) ACS Appl Mater Interfaces , vol.4 , pp. 1822-1830
    • Li, W.1    Wu, Y.2    Zhang, Q.3    Tian, H.4    Zhu, W.5
  • 29
    • 84890279710 scopus 로고    scopus 로고
    • Influence of conjugated π-linker in D-D-π-A indoline dyes: Towards long-term stable and efficient dye-sensitized solar cells with high photovoltage
    • B. Liu, B. Wang, R. Wang, L. Gao, S. Huo, and Q.L. Liu et al. Influence of conjugated π-linker in D-D-π-A indoline dyes: towards long-term stable and efficient dye-sensitized solar cells with high photovoltage J Mater Chem A 2 2014 804 812
    • (2014) J Mater Chem A , vol.2 , pp. 804-812
    • Liu, B.1    Wang, B.2    Wang, R.3    Gao, L.4    Huo, S.5    Liu, Q.L.6
  • 30
    • 84879080540 scopus 로고    scopus 로고
    • Theoretical insights into photoinduced charge transfer and catalysis at oxide interfaces
    • A.V. Akimov, A.J. Neukirch, and O.V. Prezhdo Theoretical insights into photoinduced charge transfer and catalysis at oxide interfaces Chem Rev 113 2013 4496 4565
    • (2013) Chem Rev , vol.113 , pp. 4496-4565
    • Akimov, A.V.1    Neukirch, A.J.2    Prezhdo, O.V.3
  • 31
    • 84874621761 scopus 로고    scopus 로고
    • First principles design of dye molecules with ullazine donor for dye sensitized solar cells
    • J. Feng, Y. Jiao, W. Ma, M.K. Nazeeruddin, M. Grätzel, and S. Meng First principles design of dye molecules with ullazine donor for dye sensitized solar cells J Phys Chem C 117 2013 3772 3778
    • (2013) J Phys Chem C , vol.117 , pp. 3772-3778
    • Feng, J.1    Jiao, Y.2    Ma, W.3    Nazeeruddin, M.K.4    Grätzel, M.5    Meng, S.6
  • 34
    • 77149163036 scopus 로고    scopus 로고
    • How the nature of triphenylamine-polyene dyes in dye-sensitized solar cells affects the open-circuit voltage and electron lifetimes
    • T. Marinado, K. Nonomura, J. Nissfolk, M.K. Karlsson, D.P. Hagberg, and L. Sun et al. How the nature of triphenylamine-polyene dyes in dye-sensitized solar cells affects the open-circuit voltage and electron lifetimes Langmuir 26 2009 2592 2598
    • (2009) Langmuir , vol.26 , pp. 2592-2598
    • Marinado, T.1    Nonomura, K.2    Nissfolk, J.3    Karlsson, M.K.4    Hagberg, D.P.5    Sun, L.6
  • 35
    • 66749171737 scopus 로고    scopus 로고
    • High open-circuit voltage solid-state dye-sensitized solar cells with organic dye
    • P. Chen, J.H. Yum, F.D. Angelis, E. Mosconi, S. Fantacci, and S.-J. Moon et al. High open-circuit voltage solid-state dye-sensitized solar cells with organic dye Nano Lett 9 2009 2487 2492
    • (2009) Nano Lett , vol.9 , pp. 2487-2492
    • Chen, P.1    Yum, J.H.2    Angelis, F.D.3    Mosconi, E.4    Fantacci, S.5    Moon, S.-J.6
  • 36
    • 84877652813 scopus 로고    scopus 로고
    • The effects of various anchoring groups on optical and electronic properties of dyes in dye-sensitized solar cells
    • L.-N. Yang, Z.-Z. Sun, S.-L. Chen, and Z.-S. Li The effects of various anchoring groups on optical and electronic properties of dyes in dye-sensitized solar cells Dye Pigment 99 2013 29 35
    • (2013) Dye Pigment , vol.99 , pp. 29-35
    • Yang, L.-N.1    Sun, Z.-Z.2    Chen, S.-L.3    Li, Z.-S.4
  • 37
    • 84867061520 scopus 로고    scopus 로고
    • How to design more efficient organic dyes for dye-sensitized solar cells? Adding more sp2-hybridized nitrogen in the triphenylamine donor
    • S.-L. Chen, L.-N. Yang, and Z.-S. Li How to design more efficient organic dyes for dye-sensitized solar cells? Adding more sp2-hybridized nitrogen in the triphenylamine donor J Power Sources 223 2013 86 93
    • (2013) J Power Sources , vol.223 , pp. 86-93
    • Chen, S.-L.1    Yang, L.-N.2    Li, Z.-S.3
  • 38
    • 36849118773 scopus 로고
    • On the theory of electron-transfer reactions. VI. Unified treatment for homogeneous and electrode reactions
    • R.A. Marcus On the theory of electron-transfer reactions. VI. Unified treatment for homogeneous and electrode reactions J Chem Phys 43 1965 679 701
    • (1965) J Chem Phys , vol.43 , pp. 679-701
    • Marcus, R.A.1
  • 39
    • 18944398055 scopus 로고    scopus 로고
    • Ultrafast electron transfer at the molecule-semiconductor nanoparticle interface
    • N.A. Anderson, and T. Lian Ultrafast electron transfer at the molecule-semiconductor nanoparticle interface Annu Rev Phys Chem 56 2005 491 519
    • (2005) Annu Rev Phys Chem , vol.56 , pp. 491-519
    • Anderson, N.A.1    Lian, T.2
  • 40
    • 68049129536 scopus 로고    scopus 로고
    • Structures and excitation energies of Zn-tetraarylporphyrin analogues: A theoretical study
    • M.P. Balanay, and D.H. Kim Structures and excitation energies of Zn-tetraarylporphyrin analogues: a theoretical study J Mol Struct Theochem 910 2009 20 26
    • (2009) J Mol Struct Theochem , vol.910 , pp. 20-26
    • Balanay, M.P.1    Kim, D.H.2
  • 41
    • 33744614883 scopus 로고
    • Natural hybrid orbitals
    • J.P. Foster, and F. Weinhold Natural hybrid orbitals J Am Chem Soc 102 1980 7211 7218
    • (1980) J Am Chem Soc , vol.102 , pp. 7211-7218
    • Foster, J.P.1    Weinhold, F.2
  • 43
    • 49649105201 scopus 로고    scopus 로고
    • Ion-pair charge transfer complexes with intense near IR absorption: Syntheses, crystal structures, electronic spectra and DFT calculations
    • B.-Q. Yao, J.-S. Sun, Z.-F. Tian, X.-M. Ren, D.-W. Gu, and L.-J. Shen et al. Ion-pair charge transfer complexes with intense near IR absorption: syntheses, crystal structures, electronic spectra and DFT calculations Polyhedron 27 2008 2833 2844
    • (2008) Polyhedron , vol.27 , pp. 2833-2844
    • Yao, B.-Q.1    Sun, J.-S.2    Tian, Z.-F.3    Ren, X.-M.4    Gu, D.-W.5    Shen, L.-J.6
  • 44
    • 33646377800 scopus 로고    scopus 로고
    • Evaluation of functionals O3LYP, KMLYP, and MPW1K in comparison to B3LYP for selected transition-metal compounds
    • T. Strassner, and M.A. Taige Evaluation of functionals O3LYP, KMLYP, and MPW1K in comparison to B3LYP for selected transition-metal compounds J Chem Theory Comput 1 2005 848 855
    • (2005) J Chem Theory Comput , vol.1 , pp. 848-855
    • Strassner, T.1    Taige, M.A.2
  • 45
    • 33746875442 scopus 로고    scopus 로고
    • MPW1K performs much better than B3LYP in DFT calculations on reactions that proceed by proton-coupled electron transfer (PCET)
    • M. Lingwood, J.R. Hammond, D.A. Hrovat, J.M. Mayer, and W.T. Borden MPW1K performs much better than B3LYP in DFT calculations on reactions that proceed by proton-coupled electron transfer (PCET) J Chem Theory Comput 2 2006 740 745
    • (2006) J Chem Theory Comput , vol.2 , pp. 740-745
    • Lingwood, M.1    Hammond, J.R.2    Hrovat, D.A.3    Mayer, J.M.4    Borden, W.T.5
  • 46
    • 84962349001 scopus 로고    scopus 로고
    • Energies, structures, and electronic properties of molecules in solution with the C-PCM solvation model
    • M. Cossi, N. Rega, G. Scalmani, and V. Barone Energies, structures, and electronic properties of molecules in solution with the C-PCM solvation model J Comput Chem 24 2003 669 681
    • (2003) J Comput Chem , vol.24 , pp. 669-681
    • Cossi, M.1    Rega, N.2    Scalmani, G.3    Barone, V.4
  • 47
    • 84856215640 scopus 로고    scopus 로고
    • Multiwfn: A multifunctional wavefunction analyzer
    • T. Lu, and F. Chen Multiwfn: a multifunctional wavefunction analyzer J Comput Chem 33 2012 580 592
    • (2012) J Comput Chem , vol.33 , pp. 580-592
    • Lu, T.1    Chen, F.2
  • 48
    • 84874941214 scopus 로고    scopus 로고
    • Density functional theory characterization and verification of high-performance indoline dyes with D-A-π-A architecture for dye-sensitized solar cells
    • W.-L. Ding, D.-M. Wang, Z.-Y. Geng, X.-L. Zhao, and W.-B. Xu Density functional theory characterization and verification of high-performance indoline dyes with D-A-π-A architecture for dye-sensitized solar cells Dye Pigment 98 2013 125 135
    • (2013) Dye Pigment , vol.98 , pp. 125-135
    • Ding, W.-L.1    Wang, D.-M.2    Geng, Z.-Y.3    Zhao, X.-L.4    Xu, W.-B.5
  • 50
    • 84859870050 scopus 로고    scopus 로고
    • Organic dye design tools for efficient photocurrent generation in dye-sensitized solar cells: Exciton binding energy and electron acceptors
    • B.-G. Kim, C.-G. Zhen, E.-J. Jeong, J. Kieffer, and J. Kim Organic dye design tools for efficient photocurrent generation in dye-sensitized solar cells: exciton binding energy and electron acceptors Adv Funct Mater 22 2012 1606 1612
    • (2012) Adv Funct Mater , vol.22 , pp. 1606-1612
    • Kim, B.-G.1    Zhen, C.-G.2    Jeong, E.-J.3    Kieffer, J.4    Kim, J.5
  • 51
    • 67649875709 scopus 로고    scopus 로고
    • Theoretical study on photophysical properties of ambipolar spirobifluorene derivatives as efficient blue-light-emitting materials
    • X.-Q. Ran, J.-K. Feng, A.-M. Ren, W.-C. Li, L.-Y. Zou, and C.-C. Sun Theoretical study on photophysical properties of ambipolar spirobifluorene derivatives as efficient blue-light-emitting materials J Phys Chem A 113 2009 7933 7939
    • (2009) J Phys Chem A , vol.113 , pp. 7933-7939
    • Ran, X.-Q.1    Feng, J.-K.2    Ren, A.-M.3    Li, W.-C.4    Zou, L.-Y.5    Sun, C.-C.6
  • 52
    • 76449087293 scopus 로고    scopus 로고
    • Percolation paths for charge transports in N,N′-diphenyl-N, N′-di(m-tolyl)benzidine (TPD)
    • T. Yamada, T. Sato, K. Tanaka, and H. Kaji Percolation paths for charge transports in N,N′-diphenyl-N,N′-di(m-tolyl)benzidine (TPD) Org Electron 11 2010 255 265
    • (2010) Org Electron , vol.11 , pp. 255-265
    • Yamada, T.1    Sato, T.2    Tanaka, K.3    Kaji, H.4
  • 54
    • 0037714218 scopus 로고    scopus 로고
    • Charge hopping in molecular wires as a sequence of electron-transfer reactions
    • Y.A. Berlin, G.R. Hutchison, P. Rempala, M.A. Ratner, and J. Michl Charge hopping in molecular wires as a sequence of electron-transfer reactions J Phys Chem A 107 2003 3970 3980
    • (2003) J Phys Chem A , vol.107 , pp. 3970-3980
    • Berlin, Y.A.1    Hutchison, G.R.2    Rempala, P.3    Ratner, M.A.4    Michl, J.5
  • 55
    • 63249133442 scopus 로고    scopus 로고
    • A density functional theory study on photophysical properties of red light-emitting materials: Meso-substituted porphyrins
    • X.-F. Ren, A.-M. Ren, J.-K. Feng, and C.-C. Sun A density functional theory study on photophysical properties of red light-emitting materials: meso-substituted porphyrins J Photochem Photobiol A 203 2009 92 99
    • (2009) J Photochem Photobiol A , vol.203 , pp. 92-99
    • Ren, X.-F.1    Ren, A.-M.2    Feng, J.-K.3    Sun, C.-C.4
  • 56
    • 70349866147 scopus 로고    scopus 로고
    • Enhanced efficiency of organic dye-sensitized solar cells: Triphenylamine derivatives
    • J. Preat, C. Michaux, D. Jacquemin, and E.A. Perpète Enhanced efficiency of organic dye-sensitized solar cells: triphenylamine derivatives J Phys Chem C 113 2009 16821 16833
    • (2009) J Phys Chem C , vol.113 , pp. 16821-16833
    • Preat, J.1    Michaux, C.2    Jacquemin, D.3    Perpète, E.A.4
  • 57
    • 84859517055 scopus 로고    scopus 로고
    • Density functional theory study on the electronic structure of monascus dyes as photosensitizer for dye-sensitized solar cells
    • W. Sang-aroon, S. Saekow, and V. Amornkitbamrung Density functional theory study on the electronic structure of monascus dyes as photosensitizer for dye-sensitized solar cells J Photochem Photobiol A 236 2012 35 40
    • (2012) J Photochem Photobiol A , vol.236 , pp. 35-40
    • Sang-Aroon, W.1    Saekow, S.2    Amornkitbamrung, V.3
  • 58
    • 84862314044 scopus 로고    scopus 로고
    • How to design proper π-spacer order of the D-π-A dyes for DSSCs? A density functional response
    • J. Zhang, Y.-H. Kan, H.-B. Li, Y. Geng, Y. Wu, and Z.-M. Su How to design proper π-spacer order of the D-π-A dyes for DSSCs? A density functional response Dye Pigment 95 2012 313 321
    • (2012) Dye Pigment , vol.95 , pp. 313-321
    • Zhang, J.1    Kan, Y.-H.2    Li, H.-B.3    Geng, Y.4    Wu, Y.5    Su, Z.-M.6
  • 59
    • 83455235315 scopus 로고    scopus 로고
    • Density functional theory characterization and design of high-performance diarylamine-fluorene dyes with different π spacers for dye-sensitized solar cells
    • J. Zhang, H.-B. Li, S.-L. Sun, Y. Geng, Y. Wu, and Z.-M. Su Density functional theory characterization and design of high-performance diarylamine-fluorene dyes with different π spacers for dye-sensitized solar cells J Mater Chem 22 2012 568 576
    • (2012) J Mater Chem , vol.22 , pp. 568-576
    • Zhang, J.1    Li, H.-B.2    Sun, S.-L.3    Geng, Y.4    Wu, Y.5    Su, Z.-M.6
  • 60
    • 0037448507 scopus 로고    scopus 로고
    • Molecular design of coumarin dyes for efficient dye-sensitized solar cells
    • K. Hara, T. Sato, R. Katoh, A. Furube, Y. Ohga, and A. Shinpo et al. Molecular design of coumarin dyes for efficient dye-sensitized solar cells J Phys Chem B 107 2003 597 606
    • (2003) J Phys Chem B , vol.107 , pp. 597-606
    • Hara, K.1    Sato, T.2    Katoh, R.3    Furube, A.4    Ohga, Y.5    Shinpo, A.6


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