-
1
-
-
72849124207
-
Recent advances in sensitized mesoscopic solar cells
-
M. Grätzel Recent advances in sensitized mesoscopic solar cells Acc. Chem. Res. 42 2009 1788 1798
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 1788-1798
-
-
Grätzel, M.1
-
3
-
-
78449308548
-
Dye-sensitized solar cells
-
A. Hagfeldt, G. Boschloo, L. Sun, L. Kloo, and H. Pettersson Dye-sensitized solar cells Chem. Rev. 110 2010 6595 6663
-
(2010)
Chem. Rev.
, vol.110
, pp. 6595-6663
-
-
Hagfeldt, A.1
Boschloo, G.2
Sun, L.3
Kloo, L.4
Pettersson, H.5
-
4
-
-
84865339877
-
First-principles modeling of dye-sensitized solar cells: Challenges and perspectives
-
F.d.r. Labat, T. Le Bahers, I. Ciofini, and C. Adamo First-principles modeling of dye-sensitized solar cells: challenges and perspectives Acc. Chem. Res. 45 2012 1268 1277
-
(2012)
Acc. Chem. Res.
, vol.45
, pp. 1268-1277
-
-
Labat, F.D.R.1
Le Bahers, T.2
Ciofini, I.3
Adamo, C.4
-
5
-
-
84864242870
-
Cyclometalated ruthenium(II) complexes as near-IR sensitizers for high efficiency dye-sensitized solar cells
-
T. Funaki, H. Funakoshi, O. Kitao, N. Onozawa-Komatsuzaki, K. Kasuga, K. Sayama, and H. Sugihara Cyclometalated ruthenium(II) complexes as near-IR sensitizers for high efficiency dye-sensitized solar cells Angew. Chem. Int. Ed. 51 2012 7528 7531
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 7528-7531
-
-
Funaki, T.1
Funakoshi, H.2
Kitao, O.3
Onozawa-Komatsuzaki, N.4
Kasuga, K.5
Sayama, K.6
Sugihara, H.7
-
6
-
-
70349270760
-
Triarylamine: A promising core unit for efficient photovoltaic materials
-
Z. Ning, and H. Tian Triarylamine: a promising core unit for efficient photovoltaic materials Chem. Commun. 2009 5483 5495
-
(2009)
Chem. Commun.
, pp. 5483-5495
-
-
Ning, Z.1
Tian, H.2
-
7
-
-
34548214690
-
2 films by an unsymmetrical squaraine dye
-
DOI 10.1021/ja0731470
-
2 films by an unsymmetrical squaraine dye J. Am. Chem. Soc. 129 2007 10320 10321 (Pubitemid 47330234)
-
(2007)
Journal of the American Chemical Society
, vol.129
, Issue.34
, pp. 10320-10321
-
-
Yum, J.-H.1
Walter, P.2
Huber, S.3
Rentsch, D.4
Geiger, T.5
Nuesch, F.6
De Angelis, F.7
Gratzel, M.8
Nazeeruddin, M.K.9
-
8
-
-
79956105189
-
Dithienothiophene (DTT)-based dyes for dye-sensitized solar cells: Synthesis of 2,6-dibromo-DTT
-
T.-H. Kwon, V. Armel, A. Nattestad, D.R. MacFarlane, U. Bach, S.J. Lind, K.C. Gordon, W. Tang, D.J. Jones, and A.B. Holmes Dithienothiophene (DTT)-based dyes for dye-sensitized solar cells: synthesis of 2,6-dibromo-DTT J. Org. Chem. 76 2011 4088 4093
-
(2011)
J. Org. Chem.
, vol.76
, pp. 4088-4093
-
-
Kwon, T.-H.1
Armel, V.2
Nattestad, A.3
Macfarlane, D.R.4
Bach, U.5
Lind, S.J.6
Gordon, K.C.7
Tang, W.8
Jones, D.J.9
Holmes, A.B.10
-
9
-
-
84860629481
-
Dithiafulvenyl unit as a new donor for high-efficiency dye-sensitized solar cells: Synthesis and demonstration of a family of metal-free organic sensitizers
-
K. Guo, K. Yan, X. Lu, Y. Qiu, Z. Liu, J. Sun, F. Yan, W. Guo, and S. Yang Dithiafulvenyl unit as a new donor for high-efficiency dye-sensitized solar cells: synthesis and demonstration of a family of metal-free organic sensitizers Org. Lett. 14 2012 2214 2217
-
(2012)
Org. Lett.
, vol.14
, pp. 2214-2217
-
-
Guo, K.1
Yan, K.2
Lu, X.3
Qiu, Y.4
Liu, Z.5
Sun, J.6
Yan, F.7
Guo, W.8
Yang, S.9
-
10
-
-
72849106770
-
Large ϊ-Aromatic molecules as potential sensitizers for highly efficient dye-sensitized solar cells
-
H. Imahori, T. Umeyama, and S. Ito Large π-Aromatic molecules as potential sensitizers for highly efficient dye-sensitized solar cells Acc. Chem. Res. 42 2009 1809 1818
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 1809-1818
-
-
Imahori, H.1
Umeyama, T.2
Ito, S.3
-
11
-
-
80555157669
-
Porphyrin-sensitized solar cells with cobalt (II/III) based redox electrolyte exceed 12 percent efficiency
-
A. Yella, H.-W. Lee, H.N. Tsao, C. Yi, A.K. Chandiran, M.K. Nazeeruddin, E.W.-G. Diau, C.-Y. Yeh, S.M. Zakeeruddin, and M. Grätzel Porphyrin-sensitized solar cells with cobalt (II/III) based redox electrolyte exceed 12 percent efficiency Science 334 2011 629 634
-
(2011)
Science
, vol.334
, pp. 629-634
-
-
Yella, A.1
Lee, H.-W.2
Tsao, H.N.3
Yi, C.4
Chandiran, A.K.5
Nazeeruddin, M.K.6
Diau, E.W.-G.7
Yeh, C.-Y.8
Zakeeruddin, S.M.9
Grätzel, M.10
-
12
-
-
77953107732
-
Efficient electron transfer and sensitizer regeneration in stable π-extended tetrathiafulvalene-sensitized solar cells
-
S. Wenger, P.-A. Bouit, Q. Chen, J.l. Teuscher, D.D. Censo, R. Humphry-Baker, J.-E. Moser, J.L. Delgado, N. Marín, S.M. Zakeeruddin, and M. Grätzel Efficient electron transfer and sensitizer regeneration in stable π-extended tetrathiafulvalene-sensitized solar cells J. Am. Chem. Soc. 132 2010 5164 5169
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 5164-5169
-
-
Wenger, S.1
Bouit, P.-A.2
Chen, Q.3
Teuscher, J.L.4
Censo, D.D.5
Humphry-Baker, R.6
Moser, J.-E.7
Delgado, J.L.8
Marín, N.9
Zakeeruddin, S.M.10
Grätzel, M.11
-
13
-
-
83455235315
-
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
-
14
-
-
79958776457
-
2,7-Diaminofluorene-based organic dyes for dye-sensitized solar cells: Effect of auxiliary donor on optical and electrochemical properties
-
A. Baheti, P. Singh, C.-P. Lee, K.R.J. Thomas, and K.-C. Ho 2,7-Diaminofluorene-based organic dyes for dye-sensitized solar cells: effect of auxiliary donor on optical and electrochemical properties J. Org. Chem. 76 2011 4910 4920
-
(2011)
J. Org. Chem.
, vol.76
, pp. 4910-4920
-
-
Baheti, A.1
Singh, P.2
Lee, C.-P.3
Thomas, K.R.J.4
Ho, K.-C.5
-
15
-
-
18444402587
-
Synthesis, characterisation and optical spectroscopy of diynes and poly-ynes containing derivatised fluorenes in the backbone
-
DOI 10.1039/b208963g
-
M.S. Khan, M.R.A. Al-Mandhary, M.K. Al-Suti, B. Ahrens, M.F. Mahon, L. Male, P.R. Raithby, C.E. Boothby, and A. Kohler Synthesis, characterisation and optical spectroscopy of diynes and poly-ynes containing derivatised fluorenes in the backbone Dalton Trans. 2003 74 84 (Pubitemid 41542192)
-
(2003)
Dalton Transactions
, Issue.1
, pp. 74-84
-
-
Khan, M.S.1
Al-Mandhary, M.R.A.2
Al-Suti, M.K.3
Ahrens, B.4
Mahon, M.F.5
Male, L.6
Raithby, P.R.7
Boothby, C.E.8
Kohler, A.9
-
16
-
-
79955548398
-
Vinyl spacers-tuning electron transfer through fluorene-based molecular wires
-
M. Wielopolski, J. Santos, B.M. Illescas, A. Ortiz, B. Insuasty, T. Bauer, T. Clark, D.M. Guldi, and N. Martin Vinyl spacers-tuning electron transfer through fluorene-based molecular wires Energy Environ. Sci. 4 2011 765 771
-
(2011)
Energy Environ. Sci.
, vol.4
, pp. 765-771
-
-
Wielopolski, M.1
Santos, J.2
Illescas, B.M.3
Ortiz, A.4
Insuasty, B.5
Bauer, T.6
Clark, T.7
Guldi, D.M.8
Martin, N.9
-
17
-
-
72849130701
-
Alternating polyfluorenes collect solar light in polymer photovoltaics
-
O. Ingañas, F. Zhang, and M.R. Andersson Alternating polyfluorenes collect solar light in polymer photovoltaics Acc. Chem. Res. 42 2009 1731 1739
-
(2009)
Acc. Chem. Res.
, vol.42
, pp. 1731-1739
-
-
Ingañas, O.1
Zhang, F.2
Andersson, M.R.3
-
18
-
-
84859577885
-
A fluorene-modified porphyrin for efficient dye-sensitized solar cells
-
C.-H. Wu, T.-Y. Pan, S.-H. Hong, C.-L. Wang, H.-H. Kuo, Y.-Y. Chu, E.W.-G. Diau, and C.-Y. Lin A fluorene-modified porphyrin for efficient dye-sensitized solar cells Chem. Commun. 48 2012 4329 4331
-
(2012)
Chem. Commun.
, vol.48
, pp. 4329-4331
-
-
Wu, C.-H.1
Pan, T.-Y.2
Hong, S.-H.3
Wang, C.-L.4
Kuo, H.-H.5
Chu, Y.-Y.6
Diau, E.W.-G.7
Lin, C.-Y.8
-
19
-
-
78449249576
-
Efficient triphenylamine-based dyes featuring dual-role carbazole, fluorene and spirobifluorene moieties
-
P. Shen, Y. Tang, S. Jiang, H. Chen, X. Zheng, X. Wang, B. Zhao, and S. Tan Efficient triphenylamine-based dyes featuring dual-role carbazole, fluorene and spirobifluorene moieties Org. Electron. 12 2011 125 135
-
(2011)
Org. Electron.
, vol.12
, pp. 125-135
-
-
Shen, P.1
Tang, Y.2
Jiang, S.3
Chen, H.4
Zheng, X.5
Wang, X.6
Zhao, B.7
Tan, S.8
-
20
-
-
38049057789
-
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. Grätzel 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
Grätzel, M.7
-
21
-
-
33845932597
-
Molecular engineering of organic sensitizers for solar cell applications
-
DOI 10.1021/ja066376f
-
S. Kim, J.K. Lee, S.O. Kang, J. Ko, J.H. Yum, S. Fantacci, F. De Angelis, D. Di Censo, M.K. Nazeeruddin, and M. Grätzel Molecular engineering of organic sensitizers for solar cell applications J. Am. Chem. Soc. 128 2006 16701 16707 (Pubitemid 46032749)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.51
, pp. 16701-16707
-
-
Kim, S.1
Lee, J.K.2
Kang, S.O.3
Ko, J.4
Yum, J.-H.5
Fantacci, S.6
De Angelis, F.7
Di Censo, D.8
Nazeeruddin, K.9
Gratzel, M.10
-
22
-
-
77951883486
-
Acetylene-based materials in organic photovoltaics
-
A.M.Fabio Silvestri Acetylene-based materials in organic photovoltaics Int. J. Mol. Sci. 11 2010 1471 1508
-
(2010)
Int. J. Mol. Sci.
, vol.11
, pp. 1471-1508
-
-
Silvestri, A.M.F.1
-
23
-
-
81855191934
-
Geometrical effect of stilbene on the performance of organic dye-sensitized solar cells
-
Y.-D. Lin, and T.J. Chow Geometrical effect of stilbene on the performance of organic dye-sensitized solar cells J. Mater. Chem. 21 2011 14907 14916
-
(2011)
J. Mater. Chem.
, vol.21
, pp. 14907-14916
-
-
Lin, Y.-D.1
Chow, T.J.2
-
24
-
-
79960367442
-
D-π-M-π-A structured platinum acetylide sensitizer for dye-sensitized solar cells
-
W. Wu, X. Xu, H. Yang, J. Hua, X. Zhang, L. Zhang, Y. Long, and H. Tian D-π-M-π-A structured platinum acetylide sensitizer for dye-sensitized solar cells J. Mater. Chem. 21 2011 10666 10671
-
(2011)
J. Mater. Chem.
, vol.21
, pp. 10666-10671
-
-
Wu, W.1
Xu, X.2
Yang, H.3
Hua, J.4
Zhang, X.5
Zhang, L.6
Long, Y.7
Tian, H.8
-
25
-
-
84863230153
-
Narrowing band gap of platinum acetylide dye-sensitized solar cell sensitizers with thiophene π-bridges
-
W. Wu, J. Zhang, H. Yang, B. Jin, Y. Hu, J. Hua, C. Jing, Y. Long, and H. Tian Narrowing band gap of platinum acetylide dye-sensitized solar cell sensitizers with thiophene π-bridges J. Mater. Chem. 22 2012 5382 5389
-
(2012)
J. Mater. Chem.
, vol.22
, pp. 5382-5389
-
-
Wu, W.1
Zhang, J.2
Yang, H.3
Jin, B.4
Hu, Y.5
Hua, J.6
Jing, C.7
Long, Y.8
Tian, H.9
-
26
-
-
77950825027
-
Solution-processable crystalline platinum-acetylide oligomers with broadband absorption for photovoltaic cells
-
X. Zhao, C. Piliego, B. Kim, D.A. Poulsen, B. Ma, D.A. Unruh, and J.M.J. Frechet Solution-processable crystalline platinum-acetylide oligomers with broadband absorption for photovoltaic cells Chem. Mater. 22 2010 2325 2332
-
(2010)
Chem. Mater.
, vol.22
, pp. 2325-2332
-
-
Zhao, X.1
Piliego, C.2
Kim, B.3
Poulsen, D.A.4
Ma, B.5
Unruh, D.A.6
Frechet, J.M.J.7
-
27
-
-
1942504121
-
Light-Emitting Tridentate Cyclometalated Platinum(II) Complexes Containing σ-Alkynyl Auxiliaries: Tuning of Photo- and Electrophosphorescence
-
DOI 10.1021/ja0317776
-
W. Lu, B.-X. Mi, M.C.W. Chan, Z. Hui, C.-M. Che, N. Zhu, and S.-T. Lee Light-emitting tridentate cyclometalated platinum(II) complexes containing σ-alkynyl auxiliaries: tuning of photo- and electrophosphorescence J. Am. Chem. Soc. 126 2004 4958 4971 (Pubitemid 38495789)
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.15
, pp. 4958-4971
-
-
Lu, W.1
Mi, B.-X.2
Chan, M.C.W.3
Hui, Z.4
Che, C.-M.5
Zhu, N.6
Lee, S.-T.7
-
28
-
-
84855173191
-
Free-base tetraarylporphyrin covalently linked to [60]fullerene through ethynylfluorene spacer
-
C.A. Echeverry, A. Tigreros, A. Ortiz, B. Insuasty, and N. Martín Free-base tetraarylporphyrin covalently linked to [60]fullerene through ethynylfluorene spacer J. Porphyrins Phthalocyanines 15 2011 1231 1238
-
(2011)
J. Porphyrins Phthalocyanines
, vol.15
, pp. 1231-1238
-
-
Echeverry, C.A.1
Tigreros, A.2
Ortiz, A.3
Insuasty, B.4
Martín, N.5
-
29
-
-
84855898519
-
Synthesis, two-photon absorption and optical limiting properties of new linear and multi-branched bithiazole-based derivatives
-
N. He, B. Li, H. Zhang, J. Hua, and S. Jiang Synthesis, two-photon absorption and optical limiting properties of new linear and multi-branched bithiazole-based derivatives Synth. Met. 162 2012 217 224
-
(2012)
Synth. Met.
, vol.162
, pp. 217-224
-
-
He, N.1
Li, B.2
Zhang, H.3
Hua, J.4
Jiang, S.5
-
30
-
-
78649612214
-
Control over charge transfer through molecular wires by temperature and chemical structure modifications
-
M. Wielopolski, G. de Miguel Rojas, C. van der Pol, L. Brinkhaus, G. Katsukis, M.R. Bryce, T. Clark, and D.M. Guldi Control over charge transfer through molecular wires by temperature and chemical structure modifications ACS Nano 4 2010 6449 6462
-
(2010)
ACS Nano
, vol.4
, pp. 6449-6462
-
-
Wielopolski, M.1
De Miguel Rojas, G.2
Van Der Pol, C.3
Brinkhaus, L.4
Katsukis, G.5
Bryce, M.R.6
Clark, T.7
Guldi, D.M.8
-
31
-
-
33746443466
-
Synthesis and redox properties of trinuclear ruthenium-acetylide complexes with tri(ethynylphenyl)amine bridge
-
DOI 10.1039/b600736h
-
K. Onitsuka, N. Ohara, F. Takei, and S. Takahashi Synthesis and redox properties of trinuclear ruthenium-acetylide complexes with tri(ethynylphenyl) amine bridge Dalton Trans. 2006 3693 3698 (Pubitemid 44121456)
-
(2006)
Dalton Transactions
, Issue.30
, pp. 3693-3698
-
-
Onitsuka, K.1
Ohara, N.2
Takei, F.3
Takahashi, S.4
-
32
-
-
78650123346
-
Photoinduced charge separation in platinum acetylide oligomersâ €š Ć
-
C. Liao, J.E. Yarnell, K.D. Glusac, and K.S. Schanze Photoinduced charge separation in platinum acetylide oligomers‚ Ć J. Phys. Chem. B 114 2010 14763 14771
-
(2010)
J. Phys. Chem. B
, vol.114
, pp. 14763-14771
-
-
Liao, C.1
Yarnell, J.E.2
Glusac, K.D.3
Schanze, K.S.4
-
33
-
-
84864040406
-
Fluorene-based organic dyes containing acetylene linkage for dye-sensitized solar cells
-
P. Singh, A. Baheti, K.R.J. Thomas, C.-P. Lee, and K.-C. Ho Fluorene-based organic dyes containing acetylene linkage for dye-sensitized solar cells Dyes Pigm. 95 2012 523 533
-
(2012)
Dyes Pigm.
, vol.95
, pp. 523-533
-
-
Singh, P.1
Baheti, A.2
Thomas, K.R.J.3
Lee, C.-P.4
Ho, K.-C.5
-
34
-
-
80054053516
-
Organic dyes incorporating the cyclopentadithiophene moiety for efficient dye-sensitized solar cells
-
X. Cheng, S. Sun, M. Liang, Y. Shi, Z. Sun, and S. Xue Organic dyes incorporating the cyclopentadithiophene moiety for efficient dye-sensitized solar cells Dyes Pigm. 92 2012 1292 1299
-
(2012)
Dyes Pigm.
, vol.92
, pp. 1292-1299
-
-
Cheng, X.1
Sun, S.2
Liang, M.3
Shi, Y.4
Sun, Z.5
Xue, S.6
-
35
-
-
84885488558
-
A comparative study on properties of two phenoxazine-based dyes for dye-sensitized solar cells
-
H. Tan, C. Pan, G. Wang, Y. Wu, Y. Zhang, G. Yu, and M. Zhang A comparative study on properties of two phenoxazine-based dyes for dye-sensitized solar cells Dyes Pigm. 101 2014 67 73
-
(2014)
Dyes Pigm.
, vol.101
, pp. 67-73
-
-
Tan, H.1
Pan, C.2
Wang, G.3
Wu, Y.4
Zhang, Y.5
Yu, G.6
Zhang, M.7
-
36
-
-
84859903770
-
Influence of different arylamine electron donors in organic sensitizers for dye-sensitized solar cells
-
Z. Wan, C. Jia, L. Zhou, W. Huo, X. Yao, and Y. Shi Influence of different arylamine electron donors in organic sensitizers for dye-sensitized solar cells Dyes Pigm. 95 2012 41 46
-
(2012)
Dyes Pigm.
, vol.95
, pp. 41-46
-
-
Wan, Z.1
Jia, C.2
Zhou, L.3
Huo, W.4
Yao, X.5
Shi, Y.6
-
37
-
-
11944264362
-
Light-induced redox reactions in nanocrystalline systems
-
A. Hagfeldt, and M. Graetzel Light-induced redox reactions in nanocrystalline systems Chem. Rev. 95 1995 49 68
-
(1995)
Chem. Rev.
, vol.95
, pp. 49-68
-
-
Hagfeldt, A.1
Graetzel, M.2
|