Synthesis and characterization of trivalent metal porphyrin with NCS ligand for application in dye-sensitized solar cells

Solar Energy Materials and Solar Cells

Volumn 95, Issue 4, 2011, Pages 1174-1181

  Xiang, Na ^a   Zhou, Weiping ^a   Jiang, Shenghui ^a   Deng, Lijun ^a   Liu, Yijiang ^a   Tan, Zhuo ^a   Zhao, Bin ^a   Shen, Ping ^a   Tan, Songting ^a  

^a XIANGTAN UNIVERSITY   (China)

Author keywords

Dye sensitized solar cells; Gallium (III); Manganese (III); Photovoltaic performances; Porphyrin derivative

Indexed keywords

ADSORPTION BEHAVIOR; DYE-SENSITIZED SOLAR CELL; DYE-SENSITIZED SOLAR CELLS; ELECTRON-ACCEPTING MOIETIES; FILL FACTOR; METAL PORPHYRINS; OPEN-CIRCUIT PHOTOVOLTAGE; PHOTOVOLTAIC PERFORMANCE; PORPHYRIN DERIVATIVE; SECOND LIGAND; SHORT-CIRCUIT PHOTOCURRENT; TIO;

ADSORPTION; CHELATION; CONVERSION EFFICIENCY; LIGANDS; MANGANESE; PHOTOELECTROCHEMICAL CELLS; PHOTOVOLTAIC EFFECTS; PORPHYRINS; SOLAR POWER GENERATION;

SOLAR CELLS;

EID: 79951850383     PISSN: 09270248     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.solmat.2010.12.051     Document Type: Article

References (27)

1. M.A. Green The path to 25% silicon solar cell efficiency: history of silicon cell evolution Prog. Photovolt: Res. Appl. 17 2009 183 189
2. N. Robertson Optimizing dyes for dye-sensitized solar cells Angew. Chem. Int. Ed. 45 2006 2338 2345 (Pubitemid 44105108)
3. M. Grtzel Molecular photovoltaics that mimic photosynthesis Pure Appl. Chem. 73 2001 459 467
4. Y. Chiba, A. Islam, Y. Watanabe, R. Komiya, N. Koide, and L. Han Dye-sensitized solar cells with conversion efficiency of 11.1% Jpn. J. Appl. Phys. 45 2006 638 640
5. M.K. Nazeeruddin, F.D. Angelis, S. Fantacci, A. Selloni, G. Viscardi, P. Liska, S. Ito, B. Takeru, and M. Grtzel Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers J. Am. Chem. Soc. 127 2005 16835 16847 (Pubitemid 41772844)
6. 2 film J. Phys. Chem. B 106 2002 1363 1371 (Pubitemid 35276101)
7. 2 electrodes sensitized with hemicyanine derivatives J. Phys. Chem. B 104 2000 7682 9676
8. 2 nanocrystalline electrodes with aggregated cyanine dyes J. Phys. Chem. B 105 2001 9960 9965 (Pubitemid 35338606)
9. K. Hara, T. Sato, R. Katoh, A. Furube, Y. Ohga, A. Shinpo, S. Suga, K. Sayama, H. Sugihara, and H. Arakawa Molecular design of coumarin dyes for efficient dye-sensitized solar cells J. Phys. Chem. B. 107 2003 597 606
10. 2 New J. Chem. 26 2002 1155 1160 (Pubitemid 35034647)
11. 2 electrode thickness Adv. Mater. 18 2006 1202 1205
12. W.M. Campbell, K.W. Jolley, P. Wagner, K. Wagner, P.J. Walsh, K.C. Gordon, L. Schmidt-Mende, M.K. Nazeeruddin, Q. Wang, M. Grtzel, and D.L. Officer Highly efficient porphyrin sensitizers for dye-sensitized solar cells J. Phys. Chem. C. 111 2007 11760 11762 (Pubitemid 47325747)
13. Y. Liu, N. Xiang, X. Feng, P. Shen, W. Zhou, C. Weng, B. Zhao, and S.T. Tan Thiophene-linked porphyrin derivatives for dye-sensitized solar cell Chem. Commun. 2009 2499 2501
14. 2 cells J. Phys. Chem. C 113 2009 18406 18413
15. 2 films J. Phys. Chem. B 109 2005 15397 15409
16. M.K. Nazeeruddin, R.H. Baker, D.L. Officer, W.M. Campbell, A.K. Burrell, and M. Grtzel Application of metalloporphyrins in nanocrystalline dye sensitized solar cells for conversion of sunlight into electricity Langmuir 20 2004 6514 6517
17. 2 cells Chem. Commun. 20 2007 2069 2071 (Pubitemid 46959492)
18. S. Eu, S. Hayashi, T. Umeyama, Y. Matano, Y. Araki, and H. Imahori Quinoxaline fused porphyrins for dye-sensitized solar cells J. Phys. Chem. C 112 2008 4396 4405
19. T. Bessho, S.M. Zakeeruddin, C.Y. Yeh, E.W.G. Diau, and M. Grtzel Highly efficient mesoscopic dye-sensitized solar cells based on donoracceptor- substituted porphyrins Angew. Chem. Int. Ed. 49 2010 6646 6649
20. F.C. Krebs, and H. Spanggaard Antibatic photovoltaic response in zinc porphyrin linked oligothiophenes Sol. Energy Mater. Sol. Cells 88 2005 363 375 (Pubitemid 40940694)
21. J. Ikemoto, K. Takimiya, Y. Aso, T. Otsubo, M. Fujitsuka, and O. Ito Porphyrin oligothiophene fullerene triads as an efficient intramolecular electron transfer system Org. Lett. 4 2002 309 311
22. K.R.J. Thomas, Y.C. Hsu, J.T. Lin, K.M. Lee, K.C. Ho, C.H. Lai, Y.M. Cheng, and P.T. Chou 2, 3-Disubstituted thiophene-based organic dyes for solar cells Chem. Mater. 20 2008 1830 1840 (Pubitemid 351560844)
23. Z. Wang, N. Koumura, Y. Cui, M. Takahashi, H. Sekiguchi, A. Mori, T. Kubo, A. Furube, and K. Hara Hexylthiophene-functionalized carbazole dyes for efficient molecular photovoltaics: tuning of solar-cell performance by structural modification Chem. Mater. 20 2008 3993 4003
24. X.F. Wang, O. Kitao, H. Zhou, H. Tamiaki, and S. Sasaki Efficient dye sensitized solar cell based on oxo-bacteriochlorin sensitizers with broadband absorption capability J. Phys. Chem. C 113 2009 7954 7961
25. 60 cluster as an electron shuttle in a Ru(II)-polypyridyl sensitizer-based photochemical solar cell J. Phys. Chem. B 108 2004 5166 5170
26. D.P. Hagberg, T. Marinado, K.M. Karlsson, K. Nonomura, P. Qin, G. Boschloo, T. Brinck, A. Hagfeldt, and L. Sun Tuning the HOMO and LUMO energy levels of organic chromophores for dye sensitized solar cells J. Org. Chem. 72 2007 9550 9556 (Pubitemid 350231800)
27. 2 electrodes J. Phys. Chem. B 109 2005 23776 23778 (Pubitemid 43081425)