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Volumn 15, Issue 6, 2014, Pages 1205-1214

Design strategies of metal free-organic sensitizers for dye sensitized solar cells: Role of donor and acceptor monomers

Author keywords

Absorption spectra; DFT TDDFT; Donor acceptor; Dual band; Organic dyes

Indexed keywords

ABSORPTION SPECTRA; DENSITY FUNCTIONAL THEORY; DESIGN FOR TESTABILITY; MONOMERS; SOLAR CELLS;

EID: 84898609439     PISSN: 15661199     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.orgel.2014.03.022     Document Type: Article
Times cited : (45)

References (52)
  • 4
    • 34249800376 scopus 로고    scopus 로고
    • Thiophene-functionalized coumarin dye for efficient dye-sensitized solar cells: Electron lifetime improved by coadsorption of deoxycholic acid
    • DOI 10.1021/jp067872t
    • Z.S. Wang, Y. Cui, Y. Dan-Oh, C. Kasada, A. Shinpo, and K. Hara Thiophene-functionalized coumarin dye for efficient dye-sensitized solar cells: electron lifetime improved by coadsorption of deoxycholic acid J. Phys. Chem. C 111 2007 7224 7230 (Pubitemid 46854589)
    • (2007) Journal of Physical Chemistry C , vol.111 , Issue.19 , pp. 7224-7230
    • Wang, Z.-S.1    Cui, Y.2    Dan-oh, Y.3    Kasada, C.4    Shinpo, A.5    Hara, K.6
  • 5
    • 84879205509 scopus 로고    scopus 로고
    • Theoretical investigations of metal-free dyes for solar cells: Effects of electron donor and acceptor groups on sensitizers
    • N. Santhanamoorthi, K.H. Lai, F. Taufany, and J.C. Jiang Theoretical investigations of metal-free dyes for solar cells: effects of electron donor and acceptor groups on sensitizers J. Power Sources 242 2013 464 471
    • (2013) J. Power Sources , vol.242 , pp. 464-471
    • Santhanamoorthi, N.1    Lai, K.H.2    Taufany, F.3    Jiang, J.C.4
  • 6
    • 84873425052 scopus 로고    scopus 로고
    • Molecular design of porphyrins for dye-sensitized solar cells: A DFT/TDDFT study
    • N. Santhanamoorthi, C.M. Lo, and J.C. Jiang Molecular design of porphyrins for dye-sensitized solar cells: a DFT/TDDFT study J. Phys. Chem. Lett. 4 2013 524 530
    • (2013) J. Phys. Chem. Lett. , vol.4 , pp. 524-530
    • Santhanamoorthi, N.1    Lo, C.M.2    Jiang, J.C.3
  • 7
    • 0035132372 scopus 로고    scopus 로고
    • Electron transfer dynamics in nanocrystalline titanium dioxide solar cells sensitized with ruthenium or osmium polypyridyl complexes
    • D. Kuciauskas, M.S. Freund, H.B. Gray, J.R. Winkler, and N.S. Lewis Electron transfer dynamics in nanocrystalline titanium dioxide solar cells sensitized with ruthenium or osmium polypyridyl complexes J. Phys. Chem. B 105 2001 392 403
    • (2001) J. Phys. Chem. B , vol.105 , pp. 392-403
    • Kuciauskas, D.1    Freund, M.S.2    Gray, H.B.3    Winkler, J.R.4    Lewis, N.S.5
  • 8
    • 12344315646 scopus 로고    scopus 로고
    • Synthesis, structure, and properties of [Pt(II)(diimine)(dithiolate)] dyes with 3,3′-, 4,4′-, and 5,5′-disubstituted bipyridyl: Applications in dye-sensitized solar cells
    • DOI 10.1021/ic048799t
    • E.A.M. Geary, L.J. Yellowlees, L.A. Jack, I.D.H. Oswald, S. Parsons, N. Hirata, J.R. Durrant, and N. Robertson Synthesis, structure, and properties of [Pt(II)(diimine)(dithiolate)] dyes with 3,3′-,4,4′-, and 5,5′-disubstituted bipyridyl: applications in dye-sensitized solar cells Inorg. Chem. 44 2005 242 250 (Pubitemid 40129352)
    • (2005) Inorganic Chemistry , vol.44 , Issue.2 , pp. 242-250
    • Geary, E.A.M.1    Yellowlees, L.J.2    Jack, L.A.3    Oswald, I.D.H.4    Parsons, S.5    Hirata, N.6    Durrant, J.R.7    Robertson, N.8
  • 12
    • 44849127600 scopus 로고    scopus 로고
    • A new heteroleptic ruthenium sensitizer enhances the absorptivity of mesoporous titania film for a high efficiency dye-sensitized solar cell
    • DOI 10.1039/b802909a
    • F.F. Gao, Y. Wang, J. Zhang, D. Shi, M.K. Wang, R. Humphry-Baker, P. Wang, S.M. Zakeeruddin, and M. Gratzel A new heteroleptic ruthenium sensitizer enhances the absorptivity of mesoporous titania film for a high efficiency dye-sensitized solar cell Chem. Commun. 2008 2635 2637 (Pubitemid 351793829)
    • (2008) Chemical Communications , Issue.23 , pp. 2635-2637
    • Gao, F.1    Wang, Y.2    Zhang, J.3    Shi, D.4    Wang, M.5    Humphry-Baker, R.6    Wang, P.7    Zakeeruddin, S.M.8    Gratzel, M.9
  • 13
    • 0035891138 scopus 로고    scopus 로고
    • Photoelectrochemical cells
    • DOI 10.1038/35104607
    • M. Gratzel Photoelectrochemical cells Nature 414 2001 338 344 (Pubitemid 33097816)
    • (2001) Nature , vol.414 , Issue.6861 , pp. 338-344
    • Gratzel, M.1
  • 16
    • 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.R. Fischer, and P. Bauerle Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationships to design rules Angew. Chem., Int. Ed. 48 2009 2474 2499
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 2474-2499
    • Mishra, A.1    Fischer, M.K.R.2    Bauerle, P.3
  • 17
    • 56049092306 scopus 로고    scopus 로고
    • Molecular design of coumarin dyes for stable and efficient organic dye-sensitized solar cells
    • Z.S. Wang, Y. Cui, Y. Dan-Oh, C. Kasada, A. Shinpo, and K. Hara Molecular design of coumarin dyes for stable and efficient organic dye-sensitized solar cells J. Phys. Chem. C 112 2008 17011 17017
    • (2008) J. Phys. Chem. C , vol.112 , pp. 17011-17017
    • Wang, Z.S.1    Cui, Y.2    Dan-Oh, Y.3    Kasada, C.4    Shinpo, A.5    Hara, K.6
  • 18
    • 79953211839 scopus 로고    scopus 로고
    • Indoline dyes with various acceptors for dye-sensitized solar cells
    • J.Y. Kim, Y.H. Kim, and Y.S. Kim Indoline dyes with various acceptors for dye-sensitized solar cells Curr. Appl. Phys. 11 2011 S117 S121
    • (2011) Curr. Appl. Phys. , vol.11
    • Kim, J.Y.1    Kim, Y.H.2    Kim, Y.S.3
  • 21
    • 48249133983 scopus 로고    scopus 로고
    • (2) rationalized by ab initio time-domain density functional theory
    • (2) rationalized by ab initio time-domain density functional theory J. Am. Chem. Soc. 130 2008 9756 9762
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 9756-9762
    • Duncan, W.R.1    Prezhdo, O.V.2
  • 22
    • 58549109182 scopus 로고    scopus 로고
    • Controlled electron injection and transport at materials interfaces in dye sensitized solar cells
    • V. Thavasi, V. Renugopalakrishnan, R. Jose, and S. Ramakrishna Controlled electron injection and transport at materials interfaces in dye sensitized solar cells Mater. Sci. Eng. R 63 2009 81 99
    • (2009) Mater. Sci. Eng. R , vol.63 , pp. 81-99
    • Thavasi, V.1    Renugopalakrishnan, V.2    Jose, R.3    Ramakrishna, S.4
  • 23
    • 78649306747 scopus 로고    scopus 로고
    • Spectral engineering in pi-conjugated polymers with intramolecular donor-acceptor interactions
    • P.M. Beaujuge, C.M. Amb, and J.R. Reynolds Spectral engineering in pi-conjugated polymers with intramolecular donor-acceptor interactions Acc. Chem. Res. 43 2010 1396 1407
    • (2010) Acc. Chem. Res. , vol.43 , pp. 1396-1407
    • Beaujuge, P.M.1    Amb, C.M.2    Reynolds, J.R.3
  • 24
    • 84855712079 scopus 로고    scopus 로고
    • Atomistic band gap engineering in donor-acceptor polymers
    • G.L. Gibson, T.M. McCormick, and D.S. Seferos Atomistic band gap engineering in donor-acceptor polymers J. Am. Chem. Soc. 134 2012 539 547
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 539-547
    • Gibson, G.L.1    McCormick, T.M.2    Seferos, D.S.3
  • 25
    • 47749138832 scopus 로고    scopus 로고
    • New ambipolar organic semiconductors. 1. Synthesis, single-crystal structures, redox properties, and photophysics of phenoxazine-based donor-acceptor molecules
    • Y. Zhu, A.P. Kulkarni, P.T. Wu, and S.A. Jenekhe New ambipolar organic semiconductors. 1. Synthesis, single-crystal structures, redox properties, and photophysics of phenoxazine-based donor-acceptor molecules Chem. Mater. 20 2008 4200 4211
    • (2008) Chem. Mater. , vol.20 , pp. 4200-4211
    • Zhu, Y.1    Kulkarni, A.P.2    Wu, P.T.3    Jenekhe, S.A.4
  • 26
    • 0035833878 scopus 로고    scopus 로고
    • New conjugated polymers with donor-acceptor architectures: Synthesis and photophysics of carbazole-quinoline and phenothiazine-quinoline copolymers and oligomers exhibiting large intramolecular charge transfer
    • DOI 10.1021/ma0100448
    • S.A. Jenekhe, L.D. Lu, and M.M. Alam New conjugated polymers with donor-acceptor architectures: synthesis and photophysics of carbazole-quinoline and phenothiazine-quinoline copolymers and oligomers exhibiting large intramolecular charge transfer Macromolecules 34 2001 7315 7324 (Pubitemid 33025854)
    • (2001) Macromolecules , vol.34 , Issue.21 , pp. 7315-7324
    • Jenekhe, S.A.1    Lu, L.2    Alam, M.M.3
  • 27
    • 0037068838 scopus 로고    scopus 로고
    • Does the donor-acceptor concept work for designing synthetic metals? 1. Theoretical investigation of poly(3-cyano-3′-hydroxybithiophene
    • DOI 10.1021/jp020141i
    • U. Salzner Does the donor-acceptor concept work for designing synthetic metals? 1. Theoretical investigation of poly(3-cyano-3′- hydroxybithiophene) J. Phys. Chem. B 106 2002 9214 9220 (Pubitemid 35390057)
    • (2002) Journal of Physical Chemistry B , vol.106 , Issue.36 , pp. 9214-9220
    • Salzner, U.1
  • 28
    • 0037068877 scopus 로고    scopus 로고
    • Does the donor-acceptor concept work for designing synthetic metals? 2. Theoretical investigation of copolymers of 4-(dicyanomethylene)-4H-cyclopenta[2, 1-b:3,4-b′]dithiophene and 3,4-(ethylenedioxy)thiophene
    • DOI 10.1021/jp020142a
    • U. Salzner, and M.E. Kose Does the donor-acceptor concept work for designing synthetic metals? 2. Theoretical investigation of copolymers of 4-(dicyanomethylene)-4H-cyclopenta[2,1-b: 3,4-b ']dithiophene and 3,4-(ethylenedioxy)thiophene J. Phys. Chem. B 106 2002 9221 9226 (Pubitemid 35390058)
    • (2002) Journal of Physical Chemistry B , vol.106 , Issue.36 , pp. 9221-9226
    • Salzner, U.1    Kose, M.E.2
  • 29
    • 33746506728 scopus 로고    scopus 로고
    • Does the donor-acceptor concept work for designing synthetic metals? III. Theoretical investigation of copolymers between quinoid acceptors and aromatic donors
    • DOI 10.1007/s00894-005-0046-2
    • U. Salzner, O. Karalti, and S. Durdagi Does the donor-acceptor concept work for designing synthetic metals? III. Theoretical investigation of copolymers between quinoid acceptors and aromatic donors J. Mol. Model. 12 2006 687 701 (Pubitemid 44130386)
    • (2006) Journal of Molecular Modeling , vol.12 , Issue.5 , pp. 687-701
    • Salzner, U.1    Karalti, O.2    Durdagi, S.3
  • 32
    • 0000189651 scopus 로고
    • Density-functional thermochemistry. III. The role of exact exchange
    • A.D. Becke Density-functional thermochemistry. III. The role of exact exchange J. Chem. Phys. 98 1993 5648 5652
    • (1993) J. Chem. Phys. , vol.98 , pp. 5648-5652
    • Becke, A.D.1
  • 34
    • 38849172435 scopus 로고    scopus 로고
    • New triphenylamine-based dyes for dye-sensitized solar cells
    • DOI 10.1021/jp076992d
    • W. Xu, B. Peng, J. Chen, M. Liang, and F. Cai New triphenylamine-based dyes for dye-sensitized solar cells J. Phys. Chem. C 112 2008 874 880 (Pubitemid 351206064)
    • (2008) Journal of Physical Chemistry C , vol.112 , Issue.3 , pp. 874-880
    • Xu, W.1    Peng, B.2    Chen, J.3    Liang, M.4    Cai, F.5
  • 35
    • 2442673073 scopus 로고    scopus 로고
    • Highly efficient metal-free organic dyes for dye-sensitized solar cells
    • T. Horiuchi, H. Miura, and S. Uchida Highly efficient metal-free organic dyes for dye-sensitized solar cells J. Photochem. Photobiol., A 164 2004 29 32
    • (2004) J. Photochem. Photobiol., A , vol.164 , pp. 29-32
    • Horiuchi, T.1    Miura, H.2    Uchida, S.3
  • 37
    • 0001694717 scopus 로고    scopus 로고
    • Electronic structure and spectra of ruthenium diimine complexes by density functional theory and INDO/S. Comparison of the two methods
    • DOI 10.1016/S0022-328X(01)01079-8, PII S0022328X01010798
    • S.I. Gorelsky, and A.B.P. Lever Electronic structure and spectral, of ruthenium diimine complexes by density functional theory and INDO/S. Comparison of the two methods J. Organomet. Chem. 635 2001 187 196 (Pubitemid 33618338)
    • (2001) Journal of Organometallic Chemistry , vol.635 , Issue.1-2 , pp. 187-196
    • Gorelsky, S.I.1    Lever, A.B.P.2
  • 38
    • 14944352006 scopus 로고    scopus 로고
    • University of Ottawa, Ottawa, Canada
    • S.I. Gorelsky, SWizard program, in: < http://www.sg-chem.net/ >, University of Ottawa, Ottawa, Canada, 2013.
    • (2013) SWizard Program
    • Gorelsky, S.I.1
  • 39
    • 0038281434 scopus 로고    scopus 로고
    • Ionization potential, electron affinity, electronegativity, hardness, and electron excitation energy: Molecular properties from density functional theory orbital energies
    • C.G. Zhan, J.A. Nichols, and D.A. Dixon Ionization potential, electron affinity, electronegativity, hardness, and electron excitation energy: molecular properties from density functional theory orbital energies J. Phys. Chem. A 107 2003 4184 4195
    • (2003) J. Phys. Chem. A , vol.107 , pp. 4184-4195
    • Zhan, C.G.1    Nichols, J.A.2    Dixon, D.A.3
  • 41
    • 38049057789 scopus 로고    scopus 로고
    • Highly efficient and thermally stable organic sensitizers for solvent-free dye-sensitized solar cells
    • H. Choi, C. Baik, S.O. Kang, J. Ko, M.S. Kang, M.K. Nazeeruddin, and M. Gratzel Highly efficient and thermally stable organic sensitizers for solvent-free dye-sensitized solar cells Angew. Chem., Int. Ed. 47 2008 327 330
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 327-330
    • Choi, H.1    Baik, C.2    Kang, S.O.3    Ko, J.4    Kang, M.S.5    Nazeeruddin, M.K.6    Gratzel, M.7
  • 42
    • 84861185628 scopus 로고    scopus 로고
    • The effect of conjugated spacer on novel carbazole derivatives for dye-sensitized solar cells: Density functional theory/time-dependent density functional theory study
    • S. Jungsuttiwong, T. Yakhanthip, Y. Surakhot, J. Khunchalee, T. Sudyoadsuk, V. Promarak, N. Kungwan, and S. Namuangruk The effect of conjugated spacer on novel carbazole derivatives for dye-sensitized solar cells: density functional theory/time-dependent density functional theory study J. Comput. Chem. 33 2012 1517 1523
    • (2012) J. Comput. Chem. , vol.33 , pp. 1517-1523
    • Jungsuttiwong, S.1    Yakhanthip, T.2    Surakhot, Y.3    Khunchalee, J.4    Sudyoadsuk, T.5    Promarak, V.6    Kungwan, N.7    Namuangruk, S.8
  • 44
    • 62149100634 scopus 로고    scopus 로고
    • Structurally simple dipolar organic dyes featuring 1,3-cyclohexadiene conjugated unit for dye-sensitized solar cells
    • K.F. Chen, Y.C. Hsu, Q.Y. Wu, M.C.P. Yeh, and S.S. Sun Structurally simple dipolar organic dyes featuring 1,3-cyclohexadiene conjugated unit for dye-sensitized solar cells Org. Lett. 11 2009 377 380
    • (2009) Org. Lett. , vol.11 , pp. 377-380
    • Chen, K.F.1    Hsu, Y.C.2    Wu, Q.Y.3    Yeh, M.C.P.4    Sun, S.S.5
  • 46
    • 77950587669 scopus 로고    scopus 로고
    • Synchronously reduced surface states, charge recombination, and light absorption length for high-performance organic dye-sensitized solar cells
    • R.Z. Li, J.Y. Liu, N. Cai, M. Zhang, and P. Wang Synchronously reduced surface states, charge recombination, and light absorption length for high-performance organic dye-sensitized solar cells J. Phys. Chem. B 114 2010 4461 4464
    • (2010) J. Phys. Chem. B , vol.114 , pp. 4461-4464
    • Li, R.Z.1    Liu, J.Y.2    Cai, N.3    Zhang, M.4    Wang, P.5
  • 47
    • 47649107749 scopus 로고    scopus 로고
    • Hexylthiophene-functionalized carbazole dyes for efficient molecular photovoltaics: Tuning of solar-cell performance by structural modification
    • Z.S. Wang, N. Koumura, Y. Cui, M. Takahashi, H. Sekiguchi, A. Mori, T. Kubo, A. Furube, and K. Hara Hexylthiophene-functionalized carbazole dyes for efficient molecular photovoltaics: tuning of solar-cell performance by structural modification Chem. Mater. 20 2008 3993 4003
    • (2008) Chem. Mater. , vol.20 , pp. 3993-4003
    • Wang, Z.S.1    Koumura, N.2    Cui, Y.3    Takahashi, M.4    Sekiguchi, H.5    Mori, A.6    Kubo, T.7    Furube, A.8    Hara, K.9
  • 49
    • 0001320022 scopus 로고    scopus 로고
    • Acid-base equilibria of (2,2′-bipyridyl-4,4′-dicarboxylic acid)ruthenium(II) complexes and the effect of protonation on charge-transfer sensitization of nanocrystalline titania
    • M.K. Nazeeruddin, S.M. Zakeeruddin, R. Humphry-Baker, M. Jirousek, P. Liska, N. Vlachopoulos, V. Shklover, C.H. Fischer, and M. Gratzel Acid-base equilibria of (2,2′-bipyridyl-4,4′-dicarboxylic acid)ruthenium(II) complexes and the effect of protonation on charge-transfer sensitization of nanocrystalline titania Inorg. Chem. 38 1999 6298 6305
    • (1999) Inorg. Chem. , vol.38 , pp. 6298-6305
    • Nazeeruddin, M.K.1    Zakeeruddin, S.M.2    Humphry-Baker, R.3    Jirousek, M.4    Liska, P.5    Vlachopoulos, N.6    Shklover, V.7    Fischer, C.H.8    Gratzel, M.9
  • 51
    • 65249130669 scopus 로고    scopus 로고
    • Dye-sensitized solar cells with a high absorptivity ruthenium sensitizer featuring a 2-(hexylthio)thiophene conjugated bipyridine
    • Y.M. Cao, Y. Bai, Q.J. Yu, Y.M. Cheng, S. Liu, D. Shi, F.F. Gao, and P. Wang Dye-sensitized solar cells with a high absorptivity ruthenium sensitizer featuring a 2-(hexylthio)thiophene conjugated bipyridine J. Phys. Chem. C 113 2009 6290 6297
    • (2009) J. Phys. Chem. C , vol.113 , pp. 6290-6297
    • Cao, Y.M.1    Bai, Y.2    Yu, Q.J.3    Cheng, Y.M.4    Liu, S.5    Shi, D.6    Gao, F.F.7    Wang, P.8


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