Sensitization of TiO2 by polypyridine dyes -: Role of the electron donor

被引:103
作者
Bernard, MC [1 ]
Cachet, H
Falaras, P
Hugot-Le Goff, A
Kalbac, M
Lukes, I
Oanh, NT
Stergiopoulos, T
Arabatzis, I
机构
[1] UPMC, CNRS, UPR 15, F-75252 Paris 05, France
[2] NCSR Demokritos, Inst Phys Chem, Athens, Greece
[3] Charles Univ Prague, Dept Chem, CZ-12840 Prague 2, Czech Republic
[4] INCST, Inst Mat Sci, Hanoi, Vietnam
关键词
D O I
10.1149/1.1543951
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Dye-sensitized photoelectrochemical cells (DSSC) are characterized by electrochemical impedance spectroscopy (EIS) and Raman spectroscopy during their polarization. Cells realized with a dye recently synthesized in one of our laboratories, containing two terpyridyl (terpy) ligands, are compared with cells using commercial dyes (Ru535 and Ru620) containing isothiocyanates and either bipyridyl (bpy) or terpy ligands. Here, two points are emphasized, first, the role of the functional group (carboxylate or phosphonate) which ensures the linkage to TiO2 and, second, the role of the redox couple (I-/I-3(-)) present in the electrolyte which can react with the dye D to give unwanted intermediate species. Two species, each of them giving a characteristic Raman band in the low wavenumber range, are characterized by Raman spectroscopy. The first of these species is triiodide; the nature of the second one, which directly implies the oxidized form of dye, D+, is discussed. During the DSSC functioning, EIS allows one to discriminate three potential ranges, the photocurrent plateau, the recombination range, and the direct current range when the voltage decreases from anodic to cathodic. The second intermediate exists only in the photocurrent plateau, while I-3(-) exists also in the recombination range. These results do not depend on the nature (bpy or terpy) of the ligand. (C) 2003 The Electrochemical Society.
引用
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页码:E155 / E164
页数:10
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