參考文獻 |
1. Jaeger-Waldau, A., Photovoltaics and renewable energies in Europe. Renewable & Sustainable Energy Reviews 2007, 11 (7), 1414-1437.
2. 黃建昇, 工業材料雜誌, 2003, 11月, 150.
3. Green, M. A.; Emery, K.; Hishikawa, Y.; Warta, W., Solar cell efficiency tables (version 37). Progress in Photovoltaics 2011, 19 (1), 84-92.
4. 太陽電池 總編輯:黃惠良、曾百亨
5. Guha, S.; Yang, J.; Williamson, D. L.; Lubianiker, Y.; Cohen, J. D.; Mahan, A. H., Structural, defect, and device behavior of hydrogenated amorphous Si near and above the onset of microcrystallinity. Applied Physics Letters 1999, 74 (13), 1860-1862.
6. http://www.solar-sse.com/cts.htm
7. http://www.moneydj.com/KMDJ
8. http://pvlab.ioffe.ru/about/single_junction_solar_cells.html
9. http://sharp-world.com/corporate/news/120531.html
10. Cheng, Y.-J.; Yang, S.-H.; Hsu, C.-S., Synthesis of Conjugated Polymers for Organic Solar Cell Applications. Chem Rev 2009, 109 (11), 5868-5923.
11. Forrest, S. R., The limits to organic photovoltaic cell efficiency. Mrs Bulletin 2005, 30 (1), 28-32.
12. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search-c/view_etd?URN=etd-0719106-233414
13. Tsubomura, H.; Matsumura, M.; Nomura, Y.; Amamiya, T., DYE SENSITIZED ZINC-OXIDE - AQUEOUS-ELECTROLYTE - PLATINUM PHOTOCELL. Nature 1976, 261 (5559), 402-403.
14. Oregan, B.; Gratzel, M., A LOW-COST, HIGH-EFFICIENCY SOLAR-CELL BASED ON DYE-SENSITIZED COLLOIDAL TIO2 FILMS. Nature 1991, 353 (6346), 737-740.
15. (a) Nazeeruddin, M. K.; Kay, A.; Rodicio, I.; Humphrybaker, R.; Muller, E.; Liska, P.; Vlachopoulos, N.; Gratzel, M., CONVERSION OF LIGHT TO ELECTRICITY BY CIS-X2BIS(2,2’’-BIPYRIDYL-4,4’’-DICARBOXYLATE)RUTHENIUM(II) CHARGE-TRANSFER SENSITIZERS (X = CL-, BR-, I-, CN-, AND SCN-) ON NANOCRYSTALLINE TIO2 ELECTRODES. Journal of the American Chemical Society 1993, 115 (14), 6382-6390; (b) Gratzel, M., Conversion of sunlight to electric power by nanocrystalline dye-sensitized solar cells. Journal of Photochemistry and Photobiology a-Chemistry 2004, 164 (1-3), 3-14.
16. (a) Nazeeruddin, M. K.; Pechy, P.; Renouard, T.; Zakeeruddin, S. M.; Humphry-Baker, R.; Comte, P.; Liska, P.; Cevey, L.; Costa, E.; Shklover, V.; Spiccia, L.; Deacon, G. B.; Bignozzi, C. A.; Gratzel, M., Engineering of efficient panchromatic sensitizers for nanocrystalline TiO2-based solar cells. Journal of the American Chemical Society 2001, 123 (8), 1613-1624; (b) Chiba, Y.; Islam, A.; Watanabe, Y.; Komiya, R.; Koide, N.; Han, L., Dye-sensitized solar cells with conversion efficiency of 11.1%. Japanese Journal of Applied Physics Part 2-Letters & Express Letters 2006, 45 (24-28), L638-L640.
17. (a) Nazeeruddin, M. K.; Splivallo, R.; Liska, P.; Comte, P.; Gratzel, M., A swift dye uptake procedure for dye sensitized solar cells. Chemical Communications 2003, (12), 1456-1457; (b) Nazeeruddin, M. K.; De Angelis, F.; Fantacci, S.; Selloni, A.; Viscardi, G.; Liska, P.; Ito, S.; Bessho, T.; Gratzel, M., Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers. Journal of the American Chemical Society 2005, 127 (48), 16835-16847.
18. Yella, A.; Lee, H.-W.; Tsao, H. N.; Yi, C.; Chandiran, A. K.; Nazeeruddin, M. K.; Diau, E. W.-G.; Yeh, C.-Y.; Zakeeruddin, S. M.; Graetzel, M., Porphyrin-Sensitized Solar Cells with Cobalt (II/III)-Based Redox Electrolyte Exceed 12 Percent Efficiency. Science 2011, 334 (6056), 629-634.
19. http://www.worldscibooks.com/etextbook/p217/p217_chap08.pdf
20. Gratzel, M., Photoelectrochemical cells. Nature 2001, 414 (6861), 338-344.
21. Bach, U.; Lupo, D.; Comte, P.; Moser, J. E.; Weissortel, F.; Salbeck, J.; Spreitzer, H.; Gratzel, M., Solid-state dye-sensitized mesoporous TiO2 solar cells with high photon-to-electron conversion efficiencies. Nature 1998, 395 (6702), 583-585.
22. Martinson, A. B. F.; Hamann, T. W.; Pellin, M. J.; Hupp, J. T., New architectures for dye-senstized solar cells. Chemistry-a European Journal 2008, 14 (15), 4458-4467.
23. Hoppe, H.; Sariciftci, N. S., Organic solar cells: An overview. Journal of Materials Research 2004, 19 (7), 1924-1945.
24. Campbell, W. M.; Burrell, A. K.; Officer, D. L.; Jolley, K. W., Porphyrins as light harvesters in the dye-sensitised TiO2 solar cell. Coordination Chemistry Reviews 2004, 248 (13-14), 1363-1379.
25. 童永樑, 釕金屬染料在染料敏化太陽能電池的演進, 工業材料雜誌,2008, 255(3), 109.
26. (a) Neale, N. R.; Kopidakis, N.; van de Lagemaat, J.; Gratzel, M.; Frank, A. J., Effect of a coadsorbent on the performance of dye-sensitized TiO2 solar cells: Shielding versus band-edge movement. Journal of Physical Chemistry B 2005, 109 (49), 23183-23189; (b) Zhang, Z.; Evans, N.; Zakeeruddin, S. M.; Humphry-Baker, R.; Graetzel, M., Effects of omega-guanidinoalkyl acids as coadsorbents in dye-sensitized solar cells. Journal of Physical Chemistry C 2007, 111 (1), 398-403; (c) Wang, P.; Zakeeruddin, S. M.; Comte, P.; Charvet, R.; Humphry-Baker, R.; Gratzel, M., Enhance the performance of dye-sensitized solar cells by Co-grafting amphiphilic sensitizer and hexadecylmalonic acid on TiO2 nanocrystals. Journal of Physical Chemistry B 2003, 107 (51), 14336-14341.
27. Wang, P.; Zakeeruddin, S. M.; Humphry-Baker, R.; Moser, J. E.; Gratzel, M., Molecular-scale interface engineering of TiO2 nanocrystals: Improving the efficiency and stability of dye-sensitized solar cells. Advanced Materials 2003, 15 (24), 2101-+.
28. Kuang, D. B.; Ito, S.; Wenger, B.; Klein, C.; Moser, J. E.; Humphry-Baker, R.; Zakeeruddin, S. M.; Gratzel, M., High molar extinction coefficient heteroleptic ruthenium complexes for thin film dye-sensitized solar cells. Journal of the American Chemical Society 2006, 128 (12), 4146-4154.
29. Kuang, D.; Klein, C.; Ito, S.; Moser, J.-E.; Humphry-Baker, R.; Zakeeruddin, S. M.; Graetzel, M., High molar extinction coefficient ion-coordinating ruthenium sensitizer for efficient and stable mesoscopic dye-sensitized solar cells. Advanced Functional Materials 2007, 17 (1), 154-160.
30. Klein, C.; Nazeeruddin, M. K.; Liska, P.; Di Censo, D.; Hirata, N.; Palomares, E.; Durrant, J. R.; Gratzel, M., Engineering of a novel ruthenium sensitizer and its application in dye-sensitized solar cells for conversion of sunlight into electricity. Inorganic Chemistry 2005, 44 (2), 178-180.
31. Chen, C.-Y.; Wu, S.-J.; Wu, C.-G.; Chen, J.-G.; Ho, K.-C., A ruthenium complex with superhigh light-harvesting capacity for dye-sensitized solar cells. Angewandte Chemie-International Edition 2006, 45 (35), 5822-5825.
32. Chen, C.-Y.; Lu, H.-C.; Wu, C.-G.; Chen, J.-G.; Ho, K.-C., New ruthenium complexes containing oligoalkylthiophene-substituted 1,10-phenanthroline for nanocrystalline dye-sensitized solar cells. Advanced Functional Materials 2007, 17 (1), 29-36.
33. Jiang, K. J.; Masaki, N.; Xia, J. B.; Noda, S.; Yanagida, S., A novel ruthenium sensitizer with a hydrophobic 2-thiophen-2-yl-vinyl-conjugated bipyridyl ligand for effective dye sensitized TiO2 solar cells. Chemical Communications 2006, (23), 2460-2462.
34. Hara, K.; Tachibana, Y.; Ohga, Y.; Shinpo, A.; Suga, S.; Sayama, K.; Sugihara, H.; Arakawa, H., Dye-sensitized nanocrystalline TiO2 solar cells based on novel coumarin dyes. Solar Energy Materials and Solar Cells 2003, 77 (1), 89-103.
35. a) 葉素敏, 太陽電池之有機材料介紹(上), 工業材料雜誌 2007, 248(8), 162. b) 葉素敏, 太陽電池之有機材料介紹(下), 工業材料雜誌 2007, 249(9), 182.
36. Hara, K.; Sayama, K.; Ohga, Y.; Shinpo, A.; Suga, S.; Arakawa, H., A coumarin-derivative dye sensitized nanocrystalline TiO2 solar cell having a high solar-energy conversion efficiency up to 5.6%. Chemical Communications 2001, (6), 569-570.
37. Hara, K.; Kurashige, M.; Dan-oh, Y.; Kasada, C.; Shinpo, A.; Suga, S.; Sayama, K.; Arakawa, H., Design of new coumarin dyes having thiophene moieties for highly efficient organic-dye-sensitized solar cells. New Journal of Chemistry 2003, 27 (5), 783-785.
38. Wang, Z.-S.; Cui, Y.; Dan-oh, Y.; Kasada, C.; Shinpo, A.; Hara, K., Thiophene-functionalized coumarin dye for efficient dye-sensitized solar cells: Electron lifetime improved by coadsorption of deoxycholic acid. Journal of Physical Chemistry C 2007, 111 (19), 7224-7230.
39. Wang, Z.-S.; Cui, Y.; Dan-oh, Y.; Kasada, C.; Shinpo, A.; Hara, K., Molecular Design of Coumarin Dyes for Stable and Efficient Organic Dye-Sensitized Solar Cells. Journal of Physical Chemistry C 2008, 112 (43), 17011-17017.
40. (a) Hara, K.; Sato, T.; Katoh, R.; Furube, A.; Yoshihara, T.; Murai, M.; Kurashige, M.; Ito, S.; Shinpo, A.; Suga, S.; Arakawa, H., Novel conjugated organic dyes for efficient dye-sensitized solar cells. Advanced Functional Materials 2005, 15 (2), 246-252; (b) Hara, K.; Kurashige, M.; Ito, S.; Shinpo, A.; Suga, S.; Sayama, K.; Arakawa, H., Novel polyene dyes for highly efficient dye-sensitized solar cells. Chemical Communications 2003, (2), 252-253.
41. (a) Hagberg, D. P.; Edvinsson, T.; Marinado, T.; Boschloo, G.; Hagfeldt, A.; Sun, L., A novel organic chromophore for dye-sensitized nanostructured solar cells. Chemical Communications 2006, (21), 2245-2247; (b) Hagberg, D. P.; Yum, J.-H.; Lee, H.; De Angelis, F.; Marinado, T.; Karlsson, K. M.; Humphry-Baker, R.; Sun, L.; Hagfeldt, A.; Graetzel, M.; Nazeeruddin, M. K., Molecular engineering of organic sensitizers for dye-sensitized solar cell applications. Journal of the American Chemical Society 2008, 130 (19), 6259-6266.
42. Tian, H.; Yang, X.; Chen, R.; Zhang, R.; Hagfeldt, A.; Sunt, L., Effect of different dye baths and dye-structures on the performance of dye-sensitized solar cells based on triphenylamine dyes. Journal of Physical Chemistry C 2008, 112 (29), 11023-11033.
43. (a) Kim, C.; Choi, H.; Kim, S.; Baik, C.; Song, K.; Kang, M.-S.; Kang, S. O.; Ko, J., Molecular engineering of organic sensitizers containing p-phenylene vinylene unit for dye-sensitized solar cells. Journal of Organic Chemistry 2008, 73 (18), 7072-7079; (b) Kim, S.; Choi, H.; Baik, C.; Song, K.; Kang, S. O.; Ko, J., Synthesis of conjugated organic dyes containing alkyl substituted thiophene for solar cell. Tetrahedron 2007, 63 (46), 11436-11443.
44. Tanaka, K.; Takimiya, K.; Otsubo, T.; Kawabuchi, K.; Kajihara, S.; Harima, Y., Development and photovoltaic performance of oligothiophene-sensitized TiO2 solar cells. Chemistry Letters 2006, 35 (6), 592-593.
45. Tan, S. X.; Zhai, J.; Fang, H. J.; Jiu, T. G.; Ge, J.; Li, Y. L.; Jiang, L.; Zhu, D. B., Novel carboxylated oligothiophenes as sensitizers in photoelectric conversion systems. Chemistry-a European Journal 2005, 11 (21), 6272-6276.
46. Ooyama, Y.; Harima, Y., Molecular Designs and Syntheses of Organic Dyes for Dye-Sensitized Solar Cells. European Journal of Organic Chemistry 2009, (18), 2903-2934.
47. Koumura, N.; Wang, Z.-S.; Mori, S.; Miyashita, M.; Suzuki, E.; Hara, K., Alkyl-functionalized organic dyes for efficient molecular photovoltaics. Journal of the American Chemical Society 2006, 128 (44), 14256-14257.
48. Choi, H.; Baik, C.; Kang, S. O.; Ko, J.; Kang, M.-S.; Nazeeruddin, M. K.; Graetzel, M., Highly efficient and thermally stable organic sensitizers for solvent-free dye-sensitized solar cells. Angewandte Chemie-International Edition 2008, 47 (2), 327-330.
49. Kim, S.; Kim, D.; Choi, H.; Kang, M.-S.; Song, K.; Kang, S. O.; Ko, J., Enhanced photovoltaic performance and long-term stability of quasi-solid-state dye-sensitized solar cells via molecular engineering. Chemical Communications 2008, (40), 4951-4953.
50. Liu, W.-H.; Wu, I. C.; Lai, C.-H.; Lai, C.-H.; Chou, P.-T.; Li, Y.-T.; Chen, C.-L.; Hsu, Y.-Y.; Chi, Y., Simple organic molecules bearing a 3,4-ethylenedioxythiophene linker for efficient dye-sensitized solar cells. Chemical Communications 2008, (41), 5152-5154.
51. Thomas, K. R. J.; Hsu, Y.-C.; Lin, J. T.; Lee, K.-M.; Ho, K.-C.; Lai, C.-H.; Cheng, Y.-M.; Chou, P.-T., 2,3-disubstituted thiophene-based organic dyes for solar cells. Chemistry of Materials 2008, 20 (5), 1830-1840.
52. (a) Horiuchi, T.; Miura, H.; Uchida, S., Highly efficient metal-free organic dyes for dye-sensitized solar cells. Journal of Photochemistry and Photobiology a-Chemistry 2004, 164 (1-3), 29-32; (b) Horiuchi, T.; Miura, H.; Sumioka, K.; Uchida, S., High efficiency of dye-sensitized solar cells based on metal-free indoline dyes. Journal of the American Chemical Society 2004, 126 (39), 12218-12219; (c) Schmidt-Mende, L.; Bach, U.; Humphry-Baker, R.; Horiuchi, T.; Miura, H.; Ito, S.; Uchida, S.; Gratzel, M., Organic dye for highly efficient solid-state dye-sensitized solar cells. Advanced Materials 2005, 17 (7), 813-+; (d) Ito, S.; Zakeeruddin, S. M.; Humphry-Baker, R.; Liska, P.; Charvet, R.; Comte, P.; Nazeeruddin, M. K.; Pechy, P.; Takata, M.; Miura, H.; Uchida, S.; Gratzel, M., High-efficiency organic-dye-sensitized solar cells controlled by nanocrystalline-TiO2 electrode thickness. Advanced Materials 2006, 18 (9), 1202-+.
53. Kuang, D.; Uchida, S.; Humphry-Baker, R.; Zakeeruddin, S. M.; Graetzel, M., Organic dye-sensitized ionic liquid based solar cells: Remarkable enhancement in performance through molecular design of indoline sensitizers. Angewandte Chemie-International Edition 2008, 47 (10), 1923-1927.
54. Zeng, W.; Cao, Y.; Bai, Y.; Wang, Y.; Shi, Y.; Zhang, M.; Wang, F.; Pan, C.; Wang, P., Efficient Dye-Sensitized Solar Cells with an Organic Photosensitizer Featuring Orderly Conjugated Ethylenedioxythiophene and Dithienosilole Blocks. Chemistry of Materials 2010, 22 (5), 1915-1925.
55. Karolin, J.; Johansson, L. B. A.; Strandberg, L.; Ny, T., FLUORESCENCE AND ABSORPTION SPECTROSCOPIC PROPERTIES OF DIPYRROMETHENEBORON DIFLUORIDE (BODIPY) DERIVATIVES IN LIQUIDS, LIPID-MEMBRANES, AND PROTEINS. Journal of the American Chemical Society 1994, 116 (17), 7801-7806.
56. (a) Xie, S.-X.; Petrache, G.; Schneider, E.; Ye, Q.-Z.; Bernhardt, G.; Seifert, R.; Buschauer, A., Synthesis and pharmacological characterization of novel fluorescent histamine H-2-receptor ligands derived from aminopotentidine. Bioorganic & medicinal chemistry letters 2006, 16 (15), 3886-3890; (b) Daly, C. J.; McGrath, J. C., Fluorescent ligands, antibodies, and proteins for the study of receptors. Pharmacology & Therapeutics 2003, 100 (2), 101-118.
57. (a) Coskun, A.; Akkaya, E. U., Ion sensing coupled to resonance energy transfer: A highly selective and sensitive ratiometric fluorescent chemosensor for Ag(I) by a modular approach. Journal of the American Chemical Society 2005, 127 (30), 10464-10465; (b) Zeng, L.; Miller, E. W.; Pralle, A.; Isacoff, E. Y.; Chang, C. J., A selective turn-on fluorescent sensor for imaging copper in living cells. Journal of the American Chemical Society 2006, 128 (1), 10-11.
58. Coskun, A.; Deniz, E.; Akkaya, E. U., Effective PET and ICT switching of boradiazaindacene emission: A unimolecular, emission-mode, molecular half-subtractor with reconfigurable logic gates. Organic letters 2005, 7 (23), 5187-5189.
59. (a) Golovkova, T. A.; Kozlov, D. V.; Neckers, D. C., Synthesis and properties of novel fluorescent switches. Journal of Organic Chemistry 2005, 70 (14), 5545-5549; (b) Trieflinger, C.; Rurack, K.; Daub, M., "Turn ON/OFF your LOV light": Boron-dipyrromethene-flavin dyads as biomimetic switches derived from the LOV domain. Angewandte Chemie-International Edition 2005, 44 (15), 2288-2291.
60. Ulrich, G.; Ziessel, R.; Harriman, A., The chemistry of fluorescent bodipy dyes: Versatility unsurpassed. Angewandte Chemie-International Edition 2008, 47 (7), 1184-1201.
61. (a) Arroyo, I. J.; Hu, R.; Merino, G.; Tang, B. Z.; Pena-Cabrera, E., The Smallest and One of the Brightest. Efficient Preparation and Optical Description of the Parent Borondipyrromethene System. Journal of Organic Chemistry 2009, 74 (15), 5719-5722; (b) Tram, K.; Yan, H.; Jenkins, H. A.; Vassiliev, S.; Brucec, D., The synthesis and crystal structure of unsubstituted 4,4-difluoro-4-bora-3a, 4a-diaza-s-indacene (BODIPY). Dyes and Pigments 2009, 82 (3), 392-395; (c) Schmitt, A.; Hinkeldey, B.; Wild, M.; Jung, G., Synthesis of the Core Compound of the BODIPY Dye Class: 4,4’’-Difluoro-4-bora-(3a,4a)-diaza-s-indacene. Journal of fluorescence 2009, 19 (4), 755-758.
62. Loudet, A.; Burgess, K., BODIPY dyes and their derivatives: Syntheses and spectroscopic properties. Chem Rev 2007, 107 (11), 4891-4932.
63. Bandichhor, R.; Thivierge, C.; Bhuvanesh, N. S. P.; Burgess, K., 4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene. Acta Crystallographica Section E-Structure Reports Online 2006, 62, O4310-O4311.
64. (a) Van Patten, P. G.; Shreve, A. P.; Lindsey, J. S.; Donohoe, R. J., Energy-transfer modeling for the rational design of multiporphyrin light-harvesting arrays. Journal of Physical Chemistry B 1998, 102 (21), 4209-4216; (b) Li, F. R.; Yang, S. I.; Ciringh, Y. Z.; Seth, J.; Martin, C. H.; Singh, D. L.; Kim, D. H.; Birge, R. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S., Design, synthesis, and photodynamics of light-harvesting arrays comprised of a porphyrin and one, two, or eight boron-dipyrrin accessory pigments. Journal of the American Chemical Society 1998, 120 (39), 10001-10017; (c) Kumaresan, D.; Datta, A.; Ravikanth, A., Photophysical properties of boron-dipyrrin appended porphyrins with heteroatom cores. Chemical Physics Letters 2004, 395 (1-3), 87-91; (d) Wagner, R. W.; Lindsey, J. S.; Seth, J.; Palaniappan, V.; Bocian, D. F., Molecular optoelectronic gates. Journal of the American Chemical Society 1996, 118 (16), 3996-3997; (e) Lee, C. Y.; Hupp, J. T., Dye Sensitized Solar Cells: TiO2 Sensitization with a Bodipy-Porphyrin Antenna System. Langmuir 2010, 26 (5), 3760-3765.
65. Imahori, H.; Norieda, H.; Yamada, H.; Nishimura, Y.; Yamazaki, I.; Sakata, Y.; Fukuzumi, S., Light-harvesting and photocurrent generation by cold electrodes modified with mixed self-assembled monolayers of boron-dipyrrin and ferrocene-porphyrin-fullerene triad. Journal of the American Chemical Society 2001, 123 (1), 100-110.
66. Hattori, S.; Ohkubo, K.; Urano, Y.; Sunahara, H.; Nagano, T.; Wada, Y.; Tkachenko, N. V.; Lemmetyinen, H.; Fukuzumi, S., Charge separation in a nonfluorescent donor-acceptor dyad derived from boron dipyrromethene dye, leading to photocurrent generation. Journal of Physical Chemistry B 2005, 109 (32), 15368-15375.
67. Gabe, Y.; Urano, Y.; Kikuchi, K.; Kojima, H.; Nagano, T., Highly sensitive fluorescence probes for nitric oxide based on boron dipyrromethene chromophore-rational design of potentially useful bioimaging fluorescence probe. Journal of the American Chemical Society 2004, 126 (10), 3357-3367.
68. Erten-Ela, S.; Yilmaz, M. D.; Icli, B.; Dede, Y.; Icli, S.; Akkaya, E. U., A panchromatic boradiazaindacene (BODIPY) sensitizer for dye-sensitized solar cells. Organic letters 2008, 10 (15), 3299-3302.
69. Kolemen, S.; Cakmak, Y.; Erten-Ela, S.; Altay, Y.; Brendel, J.; Thelakkat, M.; Akkaya, E. U., Solid-State Dye-Sensitized Solar Cells Using Red and Near-IR Absorbing Bodipy Sensitizers. Organic letters 2010, 12 (17), 3812-3815.
70. Kolemen, S.; Bozdemir, O. A.; Cakmak, Y.; Barin, G.; Erten-Ela, S.; Marszalek, M.; Yum, J.-H.; Zakeeruddin, S. M.; Nazeeruddin, M. K.; Graetzel, M.; Akkaya, E. U., Optimization of distyryl-Bodipy chromophores for efficient panchromatic sensitization in dye sensitized solar cells. Chemical Science 2011, 2 (5), 949-954.
71. http://www.uni-leipzig.de/poc/
72. (a) Rousseau, T.; Cravino, A.; Bura, T.; Ulrich, G.; Ziessel, R.; Roncali, J., BODIPY derivatives as donor materials for bulk heterojunction solar cells. Chemical Communications 2009, (13), 1673-1675; (b) Rousseau, T.; Cravino, A.; Bura, T.; Ulrich, G.; Ziessel, R.; Roncali, J., Multi-donor molecular bulk heterojunction solar cells: improving conversion efficiency by synergistic dye combinations. Journal of Materials Chemistry 2009, 19 (16), 2298-2300.
73. Kumaresan, D.; Thummel, R. P.; Bura, T.; Ulrich, G.; Ziessel, R., Color Tuning in New Metal-Free Organic Sensitizers (Bodipys) for Dye-Sensitized Solar Cells. Chemistry-a European Journal 2009, 15 (26), 6335-6339.
74. Wang, J.-B.; Fang, X.-Q.; Pan, X.; Dai, S.-Y.; Song, Q.-H., New 2, 6-Modified Bodipy Sensitizers for Dye-Sensitized Solar Cells. Chemistry-an Asian Journal 2012, 7 (4), 696-700.
75. Mao, M.; Wang, J.-B.; Xiao, Z.-F.; Dai, S.-Y.; Song, Q.-H., New 2,6-modified BODIPY sensitizers for dye-sensitized solar cells. Dyes and Pigments 2012, 94 (2), 224-232.
76. Rousseau, T.; Cravino, A.; Ripaud, E.; Leriche, P.; Rihn, S.; De Nicola, A.; Ziessel, R.; Roncali, J., A tailored hybrid BODIPY-oligothiophene donor for molecular bulk heterojunction solar cells with improved performances. Chemical Communications 2010, 46 (28), 5082-5084.
77. Chi, C.-C.; Huang, Y.-J.; Chen, C.-T., Synthesis and Spectroscopic Characterization of Dual Absorption BODIPY Type Dyes and their Light Harvesting Application in Polymer-Based Bulk Hetrojunction Organic Photovoltaics. Journal of the Chinese Chemical Society 2012, 59 (3), 305-316.
78. Ito, S.; Murakami, T. N.; Comte, P.; Liska, P.; Graetzel, C.; Nazeeruddin, M. K.; Graetzel, M., Fabrication of thin film dye sensitized solar cells with solar to electric power conversion efficiency over 10%. Thin Solid Films 2008, 516 (14), 4613-4619.
79. (a) Huang, S.-T.; Hsu, Y.-C.; Yen, Y.-S.; Chou, H. H.; Lin, J. T.; Chang, C.-W.; Hsu, C.-P.; Tsai, C.; Yin, D.-J., Organic Dyes Containing a Cyanovinyl Entity in the Spacer for Solar Cells Applications. Journal of Physical Chemistry C 2008, 112 (49), 19739-19747; (b) Mo, Y.; Bai, M., Preparation and adhesion of a dual-component self-assembled dual-layer film on silicon by a dip-coating nanoparticles method. Journal of Physical Chemistry C 2008, 112 (30), 11257-11264.
80. Jones, G.; Jackson, W. R.; Choi, C.; Bergmark, W. R., SOLVENT EFFECTS ON EMISSION YIELD AND LIFETIME FOR COUMARIN LASER-DYES - REQUIREMENTS FOR A ROTATORY DECAY MECHANISM. Journal of Physical Chemistry 1985, 89 (2), 294-300.
81. Wang, P.; Zakeeruddin, S. M.; Moser, J. E.; Gratzel, M., A new ionic liquid electrolyte enhances the conversion efficiency of dye-sensitized solar cells. Journal of Physical Chemistry B 2003, 107 (48), 13280-13285.
82. www.rkiinstruments.com/pdf/ac2.pps
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