메뉴 건너뛰기




Volumn 6, Issue 5, 2014, Pages 3742-3749

TiO2-assisted photoisomerization of azo dyes using self-assembled monolayers: Case study on para -methyl red towards solar-cell applications

Author keywords

azo dye; dye sensitized solar cells; optoelectronic materials; photoisomerization; smart surface design

Indexed keywords

DENSITY FUNCTIONAL THEORY; ELECTRONIC PROPERTIES; NANOPARTICLES; OPTOELECTRONIC DEVICES; PHOTOELECTROCHEMICAL CELLS; PHOTOISOMERIZATION; SELF ASSEMBLED MONOLAYERS; SOLAR CELLS; TITANIUM DIOXIDE;

EID: 84962393605     PISSN: 19448244     EISSN: 19448252     Source Type: Journal    
DOI: 10.1021/am500308d     Document Type: Article
Times cited : (48)

References (44)
  • 1
    • 77952829313 scopus 로고    scopus 로고
    • Nanoparticles Functionalised with Reversible Molecular and Supramolecular Switches
    • Klajn, R.; Stoddart, J. F.; Grzybowski, B. A. Nanoparticles Functionalised with Reversible Molecular and Supramolecular Switches Chem. Soc. Rev. 2010, 39, 2203-2237
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 2203-2237
    • Klajn, R.1    Stoddart, J.F.2    Grzybowski, B.A.3
  • 2
    • 77952379661 scopus 로고    scopus 로고
    • Light-Driven Molecular Switches in Azobenzene Self-Assembled Monolayers: Effect of Molecular Structure on Reversible Photoisomerization and Stable Cis State
    • Han, M.; Ishikawa, D.; Honda, T.; Ito, E.; Hara, M. Light-Driven Molecular Switches in Azobenzene Self-Assembled Monolayers: Effect of Molecular Structure on Reversible Photoisomerization and Stable Cis State Chem. Commun. 2010, 46, 3598-3600
    • (2010) Chem. Commun. , vol.46 , pp. 3598-3600
    • Han, M.1    Ishikawa, D.2    Honda, T.3    Ito, E.4    Hara, M.5
  • 3
    • 77956364497 scopus 로고    scopus 로고
    • Synthesis of Functionalized Triazatriangulenes for Application in Photo-Switchable Self-Assembled Monolayers
    • Kubitschke, J.; Näther, C.; Herges, R. Synthesis of Functionalized Triazatriangulenes for Application in Photo-Switchable Self-Assembled Monolayers Eur. J. Org. Chem. 2010, 2010, 5041-5055
    • (2010) Eur. J. Org. Chem. , vol.2010 , pp. 5041-5055
    • Kubitschke, J.1    Näther, C.2    Herges, R.3
  • 4
    • 0036856343 scopus 로고    scopus 로고
    • Photoinduced Motions in Azo-Containing Polymers
    • Natansohn, A.; Rochon, P. Photoinduced Motions in Azo-Containing Polymers Chem. Rev. 2002, 102, 4139-4176
    • (2002) Chem. Rev. , vol.102 , pp. 4139-4176
    • Natansohn, A.1    Rochon, P.2
  • 5
    • 67449104979 scopus 로고    scopus 로고
    • Light Switching of Molecules on Surfaces
    • Browne, W. R.; Feringa, B. L. Light Switching of Molecules on Surfaces Annu. Rev. Phys. Chem. 2009, 60, 407-428
    • (2009) Annu. Rev. Phys. Chem. , vol.60 , pp. 407-428
    • Browne, W.R.1    Feringa, B.L.2
  • 6
    • 84855463497 scopus 로고    scopus 로고
    • Photoisomerization in Different Classes of Azobenzene
    • Bandara, H. M. D.; Burdette, S. C. Photoisomerization in Different Classes of Azobenzene Chem. Soc. Rev. 2012, 41, 1809-1825
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 1809-1825
    • Bandara, H.M.D.1    Burdette, S.C.2
  • 7
    • 0034850065 scopus 로고    scopus 로고
    • Photoreactivity of Self-Assembled Monolayers of Azobenzene or Stilbene Derivatives Capped on Colloidal Gold Clusters
    • Zhang, J.; Whitesell, J. K.; Fox, M. A. Photoreactivity of Self-Assembled Monolayers of Azobenzene or Stilbene Derivatives Capped on Colloidal Gold Clusters Chem. Mater. 2001, 13, 2323-2331
    • (2001) Chem. Mater. , vol.13 , pp. 2323-2331
    • Zhang, J.1    Whitesell, J.K.2    Fox, M.A.3
  • 10
    • 67649183443 scopus 로고    scopus 로고
    • Isomerization Reactions on Single Adsorbed Molecules
    • Morgenstern, K. Isomerization Reactions on Single Adsorbed Molecules Acc. Chem. Res. 2009, 42, 213-223
    • (2009) Acc. Chem. Res. , vol.42 , pp. 213-223
    • Morgenstern, K.1
  • 11
    • 33845779407 scopus 로고    scopus 로고
    • Photo-Driven Molecular Devices
    • Saha, S.; Stoddart, J. F. Photo-Driven Molecular Devices Chem. Soc. Rev. 2007, 36, 77-92
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 77-92
    • Saha, S.1    Stoddart, J.F.2
  • 14
    • 84857820566 scopus 로고    scopus 로고
    • The Renaissance of Dye-Sensitized Solar Cells
    • Hardin, B. E.; Snaith, H. J.; McGehee, M. D. The Renaissance of Dye-Sensitized Solar Cells Nat. Photonics 2012, 6, 162-169
    • (2012) Nat. Photonics , vol.6 , pp. 162-169
    • Hardin, B.E.1    Snaith, H.J.2    McGehee, M.D.3
  • 15
    • 0035891138 scopus 로고    scopus 로고
    • Photoelectrochemical Cells
    • Grätzel, M. Photoelectrochemical Cells Nature 2001, 414, 338-344
    • (2001) Nature , vol.414 , pp. 338-344
    • Grätzel, M.1
  • 18
    • 84962426609 scopus 로고    scopus 로고
    • Relating Electron Donor and Carboxylic Acid Anchoring Substitution Effects in Azo Dyes to Dye-Sensitized Solar Cell Performance
    • Zhang, L.; Cole, J. M.; Waddell, P. G.; Low, K. S.; Liu, X. Relating Electron Donor and Carboxylic Acid Anchoring Substitution Effects in Azo Dyes to Dye-Sensitized Solar Cell Performance ACS Sustain. Chem. Eng. 2013, 1, 1440-1452
    • (2013) ACS Sustain. Chem. Eng. , vol.1 , pp. 1440-1452
    • Zhang, L.1    Cole, J.M.2    Waddell, P.G.3    Low, K.S.4    Liu, X.5
  • 19
    • 84871530805 scopus 로고    scopus 로고
    • Isomerization and Aggregation of the Solar Cell Dye D149
    • El-Zohry, A.; Orthaber, A.; Zietz, B. Isomerization and Aggregation of the Solar Cell Dye D149 J. Phys. Chem. C 2012, 116, 26144-26153
    • (2012) J. Phys. Chem. C , vol.116 , pp. 26144-26153
    • El-Zohry, A.1    Orthaber, A.2    Zietz, B.3
  • 20
    • 4744373603 scopus 로고    scopus 로고
    • Linkers for Anchoring Sensitizers to Semiconductor Nanoparticles
    • Galoppini, E. Linkers for Anchoring Sensitizers to Semiconductor Nanoparticles Coord. Chem. Rev. 2004, 248, 1283-1297
    • (2004) Coord. Chem. Rev. , vol.248 , pp. 1283-1297
    • Galoppini, E.1
  • 22
    • 79960911211 scopus 로고    scopus 로고
    • Dye-Sensitized Solar Cells Based on Donor-Acceptor π-Conjugated Fluorescent Dyes with a Pyridine Ring as an Electron-Withdrawing Anchoring Group
    • Ooyama, Y.; Inoue, S.; Nagano, T.; Kushimoto, K.; Ohshita, J.; Imae, I.; Komaguchi, K.; Harima, Y. Dye-Sensitized Solar Cells Based on Donor-Acceptor π-Conjugated Fluorescent Dyes with a Pyridine Ring as an Electron-Withdrawing Anchoring Group Angew. Chem. Int. Ed. 2011, 123, 7567-7571
    • (2011) Angew. Chem. Int. Ed. , vol.123 , pp. 7567-7571
    • Ooyama, Y.1    Inoue, S.2    Nagano, T.3    Kushimoto, K.4    Ohshita, J.5    Imae, I.6    Komaguchi, K.7    Harima, Y.8
  • 23
    • 84866516675 scopus 로고    scopus 로고
    • Stable Dyes Containing Double Acceptors Without COOH as Anchors for Highly Efficient Dye-Sensitized Solar Cells
    • Mao, J.; He, N.; Ning, Z.; Zhang, Q.; Guo, F.; Chen, L.; Wu, W.; Hua, J.; Tian, H. Stable Dyes Containing Double Acceptors Without COOH as Anchors for Highly Efficient Dye-Sensitized Solar Cells Angew. Chem., Int. Ed. 2012, 51, 9873-9876
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 9873-9876
    • Mao, J.1    He, N.2    Ning, Z.3    Zhang, Q.4    Guo, F.5    Chen, L.6    Wu, W.7    Hua, J.8    Tian, H.9
  • 24
    • 0348110656 scopus 로고    scopus 로고
    • Assembly of an Electronically Switchable Rotaxane on the Surface of a Titanium Dioxide Nanoparticle
    • Long, B.; Nikitin, K.; Fitzmaurice, D. Assembly of an Electronically Switchable Rotaxane on the Surface of a Titanium Dioxide Nanoparticle J. Am. Chem. Soc. 2003, 125, 15490-15498
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 15490-15498
    • Long, B.1    Nikitin, K.2    Fitzmaurice, D.3
  • 28
    • 0000189651 scopus 로고
    • Density-Functional Thermochemistry. III. the Role of Exact Exchange
    • Becke, A. D. Density-Functional Thermochemistry. III. The Role of Exact Exchange J. Chem. Phys. 1993, 7, 5648-5652
    • (1993) J. Chem. Phys. , vol.7 , pp. 5648-5652
    • Becke, A.D.1
  • 29
    • 33845555195 scopus 로고
    • Self-Consistent Molecular-Orbital Methods. 22. Small Split-Valence Basis Sets for Second-Row Elements
    • Gordon, M. S.; Binkley, J. S.; Pople, J. A.; Pietro, W. J.; Hehre, W. J. Self-Consistent Molecular-Orbital Methods. 22. Small Split-Valence Basis Sets for Second-Row Elements J. Am. Chem. Soc. 1982, 104, 2797-2803
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 2797-2803
    • Gordon, M.S.1    Binkley, J.S.2    Pople, J.A.3    Pietro, W.J.4    Hehre, W.J.5
  • 35
    • 22944471420 scopus 로고    scopus 로고
    • Photoisomerization of Azobenzene from First-Principles Constrained Density-Functional Calculations
    • Tiago, M. L.; Ismail-Beigi, S.; Louie, S. G. Photoisomerization of Azobenzene from First-Principles Constrained Density-Functional Calculations J. Chem. Phys. 2005, 122, 094311
    • (2005) J. Chem. Phys. , vol.122 , pp. 094311
    • Tiago, M.L.1    Ismail-Beigi, S.2    Louie, S.G.3
  • 37
    • 84885119611 scopus 로고    scopus 로고
    • Light- and Electric-Field-Induced Switching of Thiolated Azobenzene Self-Assembled Monolayer
    • Wen, J.; Tian, Z.; Ma, J. Light- and Electric-Field-Induced Switching of Thiolated Azobenzene Self-Assembled Monolayer J. Phys. Chem. C 2013, 117, 19934-19944
    • (2013) J. Phys. Chem. C , vol.117 , pp. 19934-19944
    • Wen, J.1    Tian, Z.2    Ma, J.3
  • 38
    • 84946893847 scopus 로고
    • Electrostatic Interaction of a Solute with a Continuum. A Direct Utilizaion of Ab Initio Molecular Potentials for the Prevision of Solvent Effects
    • Miertuš, S.; Scrocco, E.; Tomasi, J. Electrostatic Interaction of a Solute with a Continuum. A Direct Utilizaion of Ab Initio Molecular Potentials for the Prevision of Solvent Effects Chem. Phys. 1981, 55, 117-129
    • (1981) Chem. Phys. , vol.55 , pp. 117-129
    • Miertuš, S.1    Scrocco, E.2    Tomasi, J.3
  • 39
    • 80053442907 scopus 로고    scopus 로고
    • Comparisons between Azo Dyes and Schiff Bases Having the Same Benzothiazole/phenol Skeleton: Syntheses, Crystal Structures and Spectroscopic Properties
    • Tao, T.; Xu, F.; Chen, X.-C.; Liu, Q.-Q.; Huang, W.; You, X.-Z. Comparisons Between Azo Dyes and Schiff Bases Having the Same Benzothiazole/phenol Skeleton: Syntheses, Crystal Structures and Spectroscopic Properties Dyes Pigm. 2012, 92, 916-922
    • (2012) Dyes Pigm. , vol.92 , pp. 916-922
    • Tao, T.1    Xu, F.2    Chen, X.-C.3    Liu, Q.-Q.4    Huang, W.5    You, X.-Z.6
  • 41
    • 84864191010 scopus 로고    scopus 로고
    • High-Conversion-Efficiency Organic Dye-Sensitized Solar Cells: Molecular Engineering on D-A-π-A Featured Organic Indoline Dyes
    • Wu, Y.; Marszalek, M.; Zakeeruddin, S. M.; Zhang, Q.; Tian, H.; Grätzel, M.; Zhu, W. High-Conversion-Efficiency Organic Dye-Sensitized Solar Cells: Molecular Engineering on D-A-π-A Featured Organic Indoline Dyes Energy Environ. Sci. 2012, 5, 8261
    • (2012) Energy Environ. Sci. , vol.5 , pp. 8261
    • Wu, Y.1    Marszalek, M.2    Zakeeruddin, S.M.3    Zhang, Q.4    Tian, H.5    Grätzel, M.6    Zhu, W.7
  • 44
    • 81855191934 scopus 로고    scopus 로고
    • Geometrical Effect of Stilbene on the Performance of Organic Dye-Sensitized Solar Cells
    • Lin, Y.-D.; Chow, T. J. Geometrical Effect of Stilbene on the Performance of Organic Dye-Sensitized Solar Cells J. Mater. Chem. 2011, 21, 14907
    • (2011) J. Mater. Chem. , vol.21 , pp. 14907
    • Lin, Y.-D.1    Chow, T.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.