-
1
-
-
84895119853
-
Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers
-
S. Mathew, A. Yella, P. Gao, R. Humphry-Baker, B.F.E. Curchod, N. Ashari-Astani, I. Tavernelli, U. Rothlisberger, M.K. Nazeeruddin, and M. Grätzel Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers Nat. Chem. 6 2014 242 247
-
(2014)
Nat. Chem.
, vol.6
, pp. 242-247
-
-
Mathew, S.1
Yella, A.2
Gao, P.3
Humphry-Baker, R.4
Curchod, B.F.E.5
Ashari-Astani, N.6
Tavernelli, I.7
Rothlisberger, U.8
Nazeeruddin, M.K.9
Grätzel, M.10
-
2
-
-
84936987992
-
Fabrication of a high-performance dye-sensitized solar cell with 12.8% conversion efficiency using organic silyl-anchor dyes
-
K. Kakiage, Y. Aoyama, T. Yano, K. Oya, T. Kyomen, and M. Hanaya Fabrication of a high-performance dye-sensitized solar cell with 12.8% conversion efficiency using organic silyl-anchor dyes Chem. Commun. 51 2015 6315 6317
-
(2015)
Chem. Commun.
, vol.51
, pp. 6315-6317
-
-
Kakiage, K.1
Aoyama, Y.2
Yano, T.3
Oya, K.4
Kyomen, T.5
Hanaya, M.6
-
3
-
-
84926204303
-
Donor/acceptor indenoperylene dye for highly efficient organic dye-sensitized solar cells
-
Z. Yao, M. Zhang, H. Wu, L. Yang, R. Li, and P. Wang Donor/acceptor indenoperylene dye for highly efficient organic dye-sensitized solar cells J. Am. Chem. Soc. 137 2015 3799 3802
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 3799-3802
-
-
Yao, Z.1
Zhang, M.2
Wu, H.3
Yang, L.4
Li, R.5
Wang, P.6
-
4
-
-
70350679017
-
Highly efficient light-harvesting ruthenium sensitizer for thin-film dye-sensitized solar cells
-
J.-D. Decoppet, J.-H. Tsai, C. Grätzel, C.-G. Wu, S.M. Zakeeruddin, and M. Grätzel Highly efficient light-harvesting ruthenium sensitizer for thin-film dye-sensitized solar cells ACS Nano 3 2009 3103 3109
-
(2009)
ACS Nano
, vol.3
, pp. 3103-3109
-
-
Decoppet, J.-D.1
Tsai, J.-H.2
Grätzel, C.3
Wu, C.-G.4
Zakeeruddin, S.M.5
Grätzel, M.6
-
5
-
-
84897714086
-
Structural effect of donor in organic dye on recombination in dye-sensitized solar cells with cobalt complex electrolyte
-
T.N. Murakami, N. Koumura, M. Kimura, and S. Mori Structural effect of donor in organic dye on recombination in dye-sensitized solar cells with cobalt complex electrolyte Langmuir 30 2014 2274 2279
-
(2014)
Langmuir
, vol.30
, pp. 2274-2279
-
-
Murakami, T.N.1
Koumura, N.2
Kimura, M.3
Mori, S.4
-
6
-
-
84881419285
-
Novel D-π-A structured Zn(II)-porphyrin dyes with bulky fluorenyl substituted electron donor moieties for dye-sensitized solar cells
-
M.S. Kang, I.T. Choi, Y.W. Kim, B.S. You, S.H. Kang, J.Y. Hong, M.J. Ju, and H.K. Kim Novel D-π-A structured Zn(II)-porphyrin dyes with bulky fluorenyl substituted electron donor moieties for dye-sensitized solar cells J. Mater. Chem. A 1 2013 9848 9852
-
(2013)
J. Mater. Chem. A
, vol.1
, pp. 9848-9852
-
-
Kang, M.S.1
Choi, I.T.2
Kim, Y.W.3
You, B.S.4
Kang, S.H.5
Hong, J.Y.6
Ju, M.J.7
Kim, H.K.8
-
7
-
-
84870519758
-
Phenothiazine-sensitized organic solar cells: Effect of dye anchor group positioning on the cell performance
-
A.S. Hart, K.C. Bikram, N.K. Subbaiyan, P.A. Karr, and F. D'Souza Phenothiazine-sensitized organic solar cells: effect of dye anchor group positioning on the cell performance ACS Appl. Mater. Interfaces 4 2012 5813 5820
-
(2012)
ACS Appl. Mater. Interfaces
, vol.4
, pp. 5813-5820
-
-
Hart, A.S.1
Bikram, K.C.2
Subbaiyan, N.K.3
Karr, P.A.4
D'Souza, F.5
-
8
-
-
34548606026
-
Phenothiazine derivatives for efficient organic dye-sensitized solar cells
-
H. Tian, X. Yang, R. Chen, Y. Pan, L. Li, A. Hagfeldt, and L. Sun Phenothiazine derivatives for efficient organic dye-sensitized solar cells Chem. Commun. 2007 3741 3743
-
(2007)
Chem. Commun.
, pp. 3741-3743
-
-
Tian, H.1
Yang, X.2
Chen, R.3
Pan, Y.4
Li, L.5
Hagfeldt, A.6
Sun, L.7
-
9
-
-
84885471372
-
Influence of spatial arrangements of π-spacer and acceptor of phenothiazine based dyes on the performance of dye-sensitized solar cells
-
Z. Iqbal, W.-Q. Wu, H. Zhang, L. Han, X. Fang, L. Wang, D.-B. Kuang, H. Meier, and D. Cao Influence of spatial arrangements of π-spacer and acceptor of phenothiazine based dyes on the performance of dye-sensitized solar cells Org. Electron. 14 2013 2662 2672
-
(2013)
Org. Electron.
, vol.14
, pp. 2662-2672
-
-
Iqbal, Z.1
Wu, W.-Q.2
Zhang, H.3
Han, L.4
Fang, X.5
Wang, L.6
Kuang, D.-B.7
Meier, H.8
Cao, D.9
-
10
-
-
76949095788
-
Efficient and stable dye-sensitized solar cells based on phenothiazine sensitizers with thiophene units
-
W. Wu, J. Yang, J. Hua, J. Tang, L. Zhang, Y. Long, and H. Tian Efficient and stable dye-sensitized solar cells based on phenothiazine sensitizers with thiophene units J. Mater. Chem. 20 2010 1772 1779
-
(2010)
J. Mater. Chem.
, vol.20
, pp. 1772-1779
-
-
Wu, W.1
Yang, J.2
Hua, J.3
Tang, J.4
Zhang, L.5
Long, Y.6
Tian, H.7
-
11
-
-
60749123439
-
A light-resistant organic sensitizer for solar-cell applications
-
J.H. Yum, D.P. Hagberg, S.J. Moon, K.M. Karlsson, T. Marinado, L. Sun, A. Hagfeldt, M.K. Nazeeruddin, and M. Grätzel A light-resistant organic sensitizer for solar-cell applications Angew. Chem. Int. Ed. 48 2009 1576 1580
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 1576-1580
-
-
Yum, J.H.1
Hagberg, D.P.2
Moon, S.J.3
Karlsson, K.M.4
Marinado, T.5
Sun, L.6
Hagfeldt, A.7
Nazeeruddin, M.K.8
Grätzel, M.9
-
12
-
-
77958012358
-
Molecular design of organic dye toward retardation of charge recombination at semiconductor/dye/electrolyte interface: Introduction of twisted π-linker
-
J. Nishida, T. Masuko, Y. Cui, K. Hara, H. Shibuya, M. Ihara, T. Hosoyama, R. Goto, S. Mori, and Y. Yamashita Molecular design of organic dye toward retardation of charge recombination at semiconductor/dye/electrolyte interface: introduction of twisted π-linker J. Phys. Chem. C 114 2010 17920 17925
-
(2010)
J. Phys. Chem. C
, vol.114
, pp. 17920-17925
-
-
Nishida, J.1
Masuko, T.2
Cui, Y.3
Hara, K.4
Shibuya, H.5
Ihara, M.6
Hosoyama, T.7
Goto, R.8
Mori, S.9
Yamashita, Y.10
-
13
-
-
84865049165
-
An oligothiophene dye with triphenylamine as side chains for efficient dye-sensitized solar cells
-
H. Shang, K. Jiang, and X. Zhan An oligothiophene dye with triphenylamine as side chains for efficient dye-sensitized solar cells Org. Electron. 13 2012 2395 2400
-
(2012)
Org. Electron.
, vol.13
, pp. 2395-2400
-
-
Shang, H.1
Jiang, K.2
Zhan, X.3
-
14
-
-
77956831984
-
Bandgap modulation in efficient n-thiophene absorbers for dye solar cell sensitization
-
E.M. Barea, R. Caballero, F. Fabregat-Santiago, P.D.L. Cruz, F. Langa, and J. Bisquert Bandgap modulation in efficient n-thiophene absorbers for dye solar cell sensitization ChemPhysChem 11 2010 245 250
-
(2010)
ChemPhysChem
, vol.11
, pp. 245-250
-
-
Barea, E.M.1
Caballero, R.2
Fabregat-Santiago, F.3
Cruz, P.D.L.4
Langa, F.5
Bisquert, J.6
-
15
-
-
84879540494
-
Facile synthesis of a bulky BPTPA donor group suitable for cobalt electrolyte based dye sensitized solar cells
-
P. Gao, Y.J. Kim, J.-H. Yum, T.W. Holcombe, M.K. Nazeeruddin, and M. Grätzel Facile synthesis of a bulky BPTPA donor group suitable for cobalt electrolyte based dye sensitized solar cells J. Mater. Chem. A 1 2013 5535 5545
-
(2013)
J. Mater. Chem. A
, vol.1
, pp. 5535-5545
-
-
Gao, P.1
Kim, Y.J.2
Yum, J.-H.3
Holcombe, T.W.4
Nazeeruddin, M.K.5
Grätzel, M.6
-
16
-
-
67449119180
-
Syntheses and properties of cyano and dicyanovinyl-substituted oligomers as organic semiconductors
-
E. Wang, Q. Meng, C. Wang, L. Li, H. Li, and W. Hu Syntheses and properties of cyano and dicyanovinyl-substituted oligomers as organic semiconductors Synth. Met. 159 2009 1298 1301
-
(2009)
Synth. Met.
, vol.159
, pp. 1298-1301
-
-
Wang, E.1
Meng, Q.2
Wang, C.3
Li, L.4
Li, H.5
Hu, W.6
-
17
-
-
12844286241
-
Ab initio molecular dynamics for liquid metals
-
G. Kresse, and J. Hafner Ab initio molecular dynamics for liquid metals Phys. Rev. B 47 1993 558 561
-
(1993)
Phys. Rev. B
, vol.47
, pp. 558-561
-
-
Kresse, G.1
Hafner, J.2
-
18
-
-
2442537377
-
Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set
-
G. Kresse, and J. Furthmuller Efficient iterative schemes for ab initio total-energy calculations using a plane-wave basis set Phys. Rev. B 54 1996 11169 11186
-
(1996)
Phys. Rev. B
, vol.54
, pp. 11169-11186
-
-
Kresse, G.1
Furthmuller, J.2
-
19
-
-
79952130294
-
-
Gaussian Inc Wallingford, CT
-
M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G.A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H.P. Hratchian, A.F. Izmaylov, J. Bloino, G. Zheng, J.L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J.A. Montgomery Jr., J.E. Peralta, F. Ogliaro, M. Bearpark, J.J. Heyd, E. Brothers, K.N. Kudin, V.N. Staroverov, T. Keith, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J.C. Burant, S.S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J.M. Millam, M. Klene, J.E. Knox, J.B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, C. Pomelli, J.W. Ochterski, R.L. Martin, K. Morokuma, V.G. Zakrzewski, G.A. Voth, P. Salvador, J.J. Dannenberg, S. Dapprich, A.D. Daniels, O. Farkas, J.B. Foresman, J.V. Ortiz, J. Cioslowski, and D.J. Fox Gaussian 09 Revision B.01 2010 Gaussian Inc Wallingford, CT
-
(2010)
Gaussian 09, Revision B.01
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Scalmani, G.7
Barone, V.8
Mennucci, B.9
Petersson, G.A.10
Nakatsuji, H.11
Caricato, M.12
Li, X.13
Hratchian, H.P.14
Izmaylov, A.F.15
Bloino, J.16
Zheng, G.17
Sonnenberg, J.L.18
Hada, M.19
Ehara, M.20
Toyota, K.21
Fukuda, R.22
Hasegawa, J.23
Ishida, M.24
Nakajima, T.25
Honda, Y.26
Kitao, O.27
Nakai, H.28
Vreven, T.29
Montgomery, J.A.30
Peralta, J.E.31
Ogliaro, F.32
Bearpark, M.33
Heyd, J.J.34
Brothers, E.35
Kudin, K.N.36
Staroverov, V.N.37
Keith, T.38
Kobayashi, R.39
Normand, J.40
Raghavachari, K.41
Rendell, A.42
Burant, J.C.43
Iyengar, S.S.44
Tomasi, J.45
Cossi, M.46
Rega, N.47
Millam, J.M.48
Klene, M.49
Knox, J.E.50
Cross, J.B.51
Bakken, V.52
Adamo, C.53
Jaramillo, J.54
Gomperts, R.55
Stratmann, R.E.56
Yazyev, O.57
Austin, A.J.58
Cammi, R.59
Pomelli, C.60
Ochterski, J.W.61
Martin, R.L.62
Morokuma, K.63
Zakrzewski, V.G.64
Voth, G.A.65
Salvador, P.66
Dannenberg, J.J.67
Dapprich, S.68
Daniels, A.D.69
Farkas, O.70
Foresman, J.B.71
Ortiz, J.V.72
Cioslowski, J.73
Fox, D.J.74
more..
-
20
-
-
84902477632
-
Carbazole-dendrimer-based donor-π-acceptor type organic dyes for dye-sensitized solar cells: Effect of the size of the carbazole dendritic donor
-
P. Thongkasee, A. Thangthong, N. Janthasing, T. Sudyoadsuk, S. Namuangruk, T. Keawin, S. Jungsuttiwong, and V. Promarak Carbazole-dendrimer-based donor-π-acceptor type organic dyes for dye-sensitized solar cells: effect of the size of the carbazole dendritic donor ACS Appl. Mater. Interfaces 6 2014 8212 8222
-
(2014)
ACS Appl. Mater. Interfaces
, vol.6
, pp. 8212-8222
-
-
Thongkasee, P.1
Thangthong, A.2
Janthasing, N.3
Sudyoadsuk, T.4
Namuangruk, S.5
Keawin, T.6
Jungsuttiwong, S.7
Promarak, V.8
-
21
-
-
52649095220
-
The donor-acceptor approach allows a black-to-transmissive switching polymeric electrochrome
-
P.M. Beaujuge, S. Ellinger, and J.R. Reynolds The donor-acceptor approach allows a black-to-transmissive switching polymeric electrochrome Nat. Mater. 7 2008 795 799
-
(2008)
Nat. Mater.
, vol.7
, pp. 795-799
-
-
Beaujuge, P.M.1
Ellinger, S.2
Reynolds, J.R.3
-
22
-
-
11944264362
-
Light-induced redox reactions in nanocrystalline systems
-
A. Hagfeldt, and M. Grätzel Light-induced redox reactions in nanocrystalline systems Chem. Rev. 95 1995 49 68
-
(1995)
Chem. Rev.
, vol.95
, pp. 49-68
-
-
Hagfeldt, A.1
Grätzel, M.2
|