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Conjugated Polymer-Based Organic Solar Cells
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Polymer-Fullerene Composite Solar Cell
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Cheng, Y.-J.1
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66149182663
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Donor-Acceptor Nanoarchitecture on Semiconducting Electrodes for Solar Energy Conversion
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Imahori, H.1
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One-Dimensional Nanostructured Semiconducting Materials for Organic Photovoltaics
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Sagawa, T.1
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7
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0038462260
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Molecular Photovoltaics
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Recent Advances in Sensitized Mesoscopic Solar Cells
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Grätzel, M.1
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11
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79951815918
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submitted
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2 Electrodes - the Key Role of Charge Recombination for Solar Cell Performance," submitted.
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2 Electrodes - The Key Role of Charge Recombination for Solar Cell Performance
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Imahori, H.1
Kang, S.2
Hayashi, H.3
Haruta, M.4
Kurata, H.5
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Canton, S.E.7
Infahsaeng, Y.8
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Pascher, T.10
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12
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70449579091
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2 Cells
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2 Cells," J. Phys. Chem. C, vol. 113, 18406-18413 (2009).
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Imahori, H.1
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Eu, S.5
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13
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72849147122
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Kinetic and Energetic Paradigms for Dye-Sensitized Solar Cells: Moving from the Ideal to the Real
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(e) B. C. O'Regan and J. R. Durrant, "Kinetic and Energetic Paradigms for Dye-Sensitized Solar Cells: Moving from the Ideal to the Real," Acc. Chem. Res., vol. 42, 1799-1808 (2009).
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O'Regan, B.C.1
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70349784869
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Metal-Free Organic Dyes for Dye-Sensitized Solar Cells: From Structure: Property Relationships to Design Rules
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54249084072
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2 Cells
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2 Cells," J. Phys. Chem. C, vol. 112, 15576-15585 (2008).
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Hayashi, S.1
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Imahori, H.8
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16
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34249275277
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Electron-Donating Perylene Tetracarboxylic Acid for Dye-Sensitized Solar Cells
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(c) Y. Shibano, T. Umeyama, Y. Matano, and H. Imahori, "Electron-Donating Perylene Tetracarboxylic Acid for Dye-Sensitized Solar Cells," Org. Lett., vol. 9, 1971-1974 (2007).
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Shibano, Y.1
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33746271910
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Optimizing Dyes for Dye-Sensitized Solar Cells
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(d) N. Robertson, "Optimizing Dyes for Dye-Sensitized Solar Cells," Angew. Chem. Int. Ed., vol. 45, 2338-2345 (2006).
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Robertson, N.1
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34249897581
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Phthalocyanines: Old Dyes, New Materials. Putting Color in Nanotechnology
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(a) G. de la Torre, C. G. Claessens, and T. Torres, " Phthalocyanines: Old Dyes, New Materials. Putting Color in Nanotechnology," Chem. Commun., 2000-2015 (2007).
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Chem. Commun.
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De La Torre, G.1
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19
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72849106770
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Large π Aromatic Molecules as Potential Sensitizers in Dye-Sensitized Solar Cells
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(b) H. Imahori, T. Umeyama, and S. Ito, "Large π Aromatic Molecules as Potential Sensitizers in Dye-Sensitized Solar Cells," Acc. Chem. Res. vol. 42, 1809-1818 (2009).
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Imahori, H.1
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20
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77953530970
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Effects of meso-Diarylamino Group of Porphyrins as Sensitizers in Dye-Sensitized Solar Cells on Optical, Electrochemical, and Photovoltaic Properties
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(c) H. Imahori, Y. Matsubara, H. Iijima, T. Umeyama, Y. Matano, S. Ito, M. Niemi, N. V. Tkachenko, and H. Lemmetyinen, "Effects of meso-Diarylamino Group of Porphyrins as Sensitizers in Dye-Sensitized Solar Cells on Optical, Electrochemical, and Photovoltaic Properties," J. Phys. Chem. C, vol. 114, 10656-10665 (2010).
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21
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42449151360
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Carboxyquinoxaline-Fused Porphyrins for Dye-Sensitized Solar Cells
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(d) S. Eu, S. Hayashi, T. Umeyama, Y. Matano, Y. Araki, and H. Imahori, "Carboxyquinoxaline-Fused Porphyrins for Dye-Sensitized Solar Cells," J. Phys. Chem. C, vol. 112, 4396-4405 (2008).
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Eu, S.1
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22
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77954061540
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Effects of π-Elongation and Fused Position of Quinoxaline-Fused Porphyrins as Sensitizers in Dye-Sensitized Solar Cells on Optical, Electrochemical, and Photovoltaic Properties
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in press
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(e) A. Kira, Y. Matsubara, H. Iijima, T. Umeyama, Y. Matano, S. Ito, M. Niemi, N. V. Tkachenko, H. Lemmetyinen, and H. Imahori, "Effects of π-Elongation and Fused Position of Quinoxaline-Fused Porphyrins as Sensitizers in Dye-Sensitized Solar Cells on Optical, Electrochemical, and Photovoltaic Properties," J. Phys. Chem. C, in press.
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J. Phys. Chem. C
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23
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34548202343
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Highly Efficient Porphyrin Sensitizers for Dye-Sensitized Solar Cells
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(f) W. M. Campbell, K. W. Jolley, P. Wagner, P. J. Walsh, K. C. Gordon, L. Schmidt-Mende, M. K. Nazeeruddin, Q. Wang, M. Grätzel, and D. Officer, "Highly Efficient Porphyrin Sensitizers for Dye-Sensitized Solar Cells," J. Phys. Chem. C, vol. 111, 11760-11762 (2007).
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Wang, Q.8
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24
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70449472907
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Design and Characterization of Highly Efficient Porphyrin Sensitizers for Green See-Through Dye-Sensitized Solar Cells
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(g) H.-P. Lu, C.-L. Mai, C.-Y. Tsia, S.-J. Hsu, C.-P. Hsieh, C.-L. Chiu, C.-Y. Yeh, and E. W.-G. Diau, "Design and Characterization of Highly Efficient Porphyrin Sensitizers for Green See-Through Dye-Sensitized Solar Cells," Phys. Chem. Chem. Phys., vol. 11, 10270-10274 (2009).
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25
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0036570053
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2 Electrode
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2 Electrode," J. Am. Chem. Soc., vol. 124, 4922-4932 (2002).
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He, J.1
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26
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33846443172
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2 Films by a Near-IR-Absorbing Unsymmetrical Zinc Phthalocyanine
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2 Films by a Near-IR-Absorbing Unsymmetrical Zinc Phthalocyanine," Angew. Chem. Int. Ed., vol. 46, 373-376 (2007).
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27
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36249026395
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Molecular Cosensitization for Efficient Panchromatic Dye-Sensitized Solar Cells
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(b) J.-J. Cíd, J.-H. Yum, S.-R. Jang, Md. K. Nazeeruddin, E. Martínez-Ferrero, E. Palomares, J. Ko, M. Grätzel, and T. Torres, "Molecular Cosensitization for Efficient Panchromatic Dye-Sensitized Solar Cells," Angew. Chem. Int. Ed., vol. 46, 8358-8362 (2007).
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28
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77950214390
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Enhancement of Incident-Photon-to-Current Conversion Efficiency for Phthalocyanine-Sensitized Solar Cells by 3D Molecular Structuralization
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(c) S. Mori, M. Nagata, Y. Nakahata, K. Yasuta, R. Goto, M. Kimura, and M. Taya, "Enhancement of Incident-Photon-to-Current Conversion Efficiency for Phthalocyanine-Sensitized Solar Cells by 3D Molecular Structuralization, ", J. Am. Chem. Soc., vol. 132, 4054-4055 (2010).
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29
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53449100945
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Synthesis of Sterically Hindered Phthalocyanines and Their Applications to Dye-Sensitized Solar Cells
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(d) S. Eu, T. Katoh, T. Umeyama, Y. Matano, and H. Imahori, "Synthesis of Sterically Hindered Phthalocyanines and Their Applications to Dye-Sensitized Solar Cells," Dalton Trans., 5476-5483 (2008).
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Eu, S.1
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Imahori, H.5
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30
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79951845769
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Synthesis and characterization of TTPc, BTPc, and HMPc will be reported elsewhere in details
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Synthesis and characterization of TTPc, BTPc, and HMPc will be reported elsewhere in details.
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