Porphyrin dyes for TiO2 sensitization

被引:218
作者
Odobel, F
Blart, E
Lagrée, M
Villieras, M
Boujtita, H
El Murr, N
Caramori, S
Bignozzi, CA
机构
[1] Fac Sci & Tech, Organ Synth Lab, UMR 6513, CNRS, F-44322 Nantes 3, France
[2] Fac Sci & Tech, Lab Anal Isotop & Electrochim Metab, UMR 6006, F-44322 Nantes 3, France
[3] Univ Ferrara, Dipartimento Chim, I-44100 Ferrara, Italy
关键词
D O I
10.1039/b210674d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of six new free base porphyrins were synthesized for use as photosensitizers in TiO2 dye-sensitized photo-electrochemical cells. The porphyrin sensitizers are attached to the TiO2 photoelectrode by phosphonic or carboxylic acid anchoring groups. These anchoring groups were placed on different substitution positions on the porphyrin moiety. The new dyes were fully characterized by absorption and emission spectroscopies, electrochemistry and photo-electrochemical spectroscopy. The photo-electrochemical performances of the sensitizers are discussed and compared to the known 5,10,15,20-tetra(4-carboxyphenyl)porphyrin sensitizer. In this study, we show that the nature of the anchoring group (phosphonic or carboxylic acids) has little impact on the photo-electrochemical performance of the cell. However, the substitution position of the anchoring group on the porphyrin strongly influences the monochromatic photon-to-electron conversion efficiency of the resulting cell. The results indicate that the electronic coupling of this type of dye with the d-band of the semiconductor is one of the key parameters in the design of efficient sensitizers.
引用
收藏
页码:502 / 510
页数:9
相关论文
共 55 条
[11]   SPECTROSCOPIC DETERMINATION OF FLAT-BAND POTENTIALS FOR POLYCRYSTALLINE TIO2 ELECTRODES IN MIXED-SOLVENT SYSTEMS [J].
ENRIGHT, B ;
REDMOND, G ;
FITZMAURICE, D .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (24) :6195-6200
[12]  
FELTON RH, 1978, PORPHYRINS, V5, pCH3
[13]   Dye sensitization of nanocrystalline tin oxide by perylene derivatives [J].
Ferrere, S ;
Zaban, A ;
Gregg, BA .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (23) :4490-4493
[14]  
FUHRHOP JH, 1973, J AM CHEM SOC, V95, P5140
[15]   Synthesis of porphyrin dyads with potential use in solar energy conversion [J].
Fungo, F ;
Otero, LA ;
Sereno, L ;
Silber, JJ ;
Durantini, EN .
JOURNAL OF MATERIALS CHEMISTRY, 2000, 10 (03) :645-650
[16]   Photosensitization of thin SnO2 nanocrystalline semiconductor film electrodes with metallodiporphyrin [J].
Fungo, F ;
Otero, L ;
Durantini, EN ;
Silber, JJ ;
Sereno, LE .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (32) :7644-7651
[17]   Phosphonate-based bipyridine dyes for stable photovoltaic devices [J].
Gillaizeau-Gauthier, I ;
Odobel, F ;
Alebbi, M ;
Argazzi, R ;
Costa, E ;
Bignozzi, CA ;
Qu, P ;
Meyer, GJ .
INORGANIC CHEMISTRY, 2001, 40 (23) :6073-6079
[18]   LIGHT-INDUCED REDOX REACTIONS IN NANOCRYSTALLINE SYSTEMS [J].
HAGFELDT, A ;
GRATZEL, M .
CHEMICAL REVIEWS, 1995, 95 (01) :49-68
[19]   Parameters influencing charge recombination kinetics in dye-sensitized nanocrystalline titanium dioxide films [J].
Haque, SA ;
Tachibana, Y ;
Willis, RL ;
Moser, JE ;
Grätzel, M ;
Klug, DR ;
Durrant, JR .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (03) :538-547
[20]   Modified phthalocyanines for efficient near-IR sensitization of nanostructured TiO2 electrode [J].
He, JJ ;
Benkö, G ;
Korodi, F ;
Polívka, T ;
Lomoth, R ;
Åkermark, B ;
Sun, LC ;
Hagfeldt, A ;
Sundström, V .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (17) :4922-4932