Structure-Function Relationships in Unsymmetrical Zinc Phthalocyanines for Dye-Sensitized Solar Cells

被引:165
作者
Cid, Juan-Jose [2 ]
Garcia-Iglesias, Miguel [2 ]
Yum, Jun-Ho [1 ]
Forneli, Amparo [3 ]
Albero, Josep [3 ]
Martinez-Ferrero, Eugenia [3 ]
Vazquez, Purificacion [2 ]
Graetzel, Michael [1 ]
Nazeeruddin, Mohammad K. [1 ]
Palomares, Emilio [3 ]
Torres, Tomas [2 ]
机构
[1] Swiss Fed Inst Technol, Sch Basic Sci, Inst Chem Sci & Engn, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[2] Univ Autonoma Madrid, Dept Quim Organ, E-28049 Madrid, Spain
[3] Inst Chem Res Catalonia ICIQ, Tarragona 43007, Spain
关键词
electron transfer; mesoporous materials; photochemistry; phthalocyanines; sensitizers; zinc; NANOCRYSTALLINE TIO2 FILMS; ELECTRON INJECTION; PHOTOPHYSICAL PROPERTIES; IR SENSITIZATION; EFFICIENT; DYADS; ACID;
D O I
10.1002/chem.200801778
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of unsymmetrical zinc phthalocyanines bearing an anchoring carboxylic function linked to the phthalocyanine ring through different spacers were designed for dye-sensitised solar cells (DSSC). The modification of the spacer group allows not only a variable distance between the dye and the nanocrystalline TiO2, but also a distinct orientation of the phthalocyanine on the semiconductor surface. The photovoltaic data show that the nature of the spacer group plays a significant role in the electron injection from the photo-excited dye into the nanocrystalline TiO2 semiconductor, the recombination rates and the efficiency of the cells. The incident monochromatic photon-to-current conversion efficiency (IPCE) for phthalocyanines bearing an insulating spacer is as low as 9%, whereas for those with a conducting spacer an outstanding IPCE 80% was obtained.
引用
收藏
页码:5130 / 5137
页数:8
相关论文
共 38 条
[1]   Dye-sensitized solar cell using a TiO2 nanocrystalline film electrode modified by an aluminum phthalocyanine and myristic acid coadsorption layer [J].
Amao, Y ;
Komori, T .
LANGMUIR, 2003, 19 (21) :8872-8875
[2]  
[Anonymous], 2007, ANGEW CHEM INT EDIT
[3]  
Aranyos V, 2001, J PORPHYR PHTHALOCYA, V5, P609, DOI 10.1002/jpp.371
[4]   Synthesis, characterization and photophysical properties of a SWNT-phthalocyanine hybrid [J].
Ballesteros, Beatriz ;
Campidelli, Stephane ;
de la Torre, Gema ;
Ehli, Christian ;
Guldi, Dirk M. ;
Prato, Maurizio ;
Torres, Tomas .
CHEMICAL COMMUNICATIONS, 2007, (28) :2950-2952
[5]   Intermittent single-molecule interfacial electron transfer dynamics [J].
Biju, V ;
Micic, M ;
Hu, DH ;
Lu, HP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (30) :9374-9381
[6]   Relaxation dynamics of ruthenium complexes in solution, PMMA and TiO2 films:: The roles of self-quenching and interfacial electron transfer [J].
Chang, Chih-Wei ;
Chou, Chung Kuang ;
Chang, I-Jy ;
Lee, Yuan-Pern ;
Diau, Eric Wei-Guang .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (35) :13288-13296
[7]   THE PHOTOPHYSICAL PROPERTIES OF A RUTHENIUM-SUBSTITUTED PHTHALOCYANINE [J].
CHARLESWORTH, P ;
TRUSCOTT, TG ;
BROOKS, RC ;
WILSON, BC .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1994, 26 (03) :277-282
[8]  
CID JJ, 2008, THESIS U AUTONOMA MA
[9]   Molecular cosensitization for efficient panchromatic dye-sensitized solar cells [J].
Cid, Juan-Jose ;
Yum, Jun-Ho ;
Jang, Song-Rim ;
Nazeeruddin, Mohammad K. ;
Ferrero, Eugenia Martinez ;
Palomares, Emilio ;
Ko, Jaejung ;
Graetzel, Michael ;
Torres, Tomas .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (44) :8358-8362
[10]   Photochemical energy conversion: from molecular dyads to solar cells [J].
Durrant, James R. ;
Haque, Saif A. ;
Palomares, Emilio .
CHEMICAL COMMUNICATIONS, 2006, (31) :3279-3289