Synthesis of a hemicyanine dye bearing two carboxylic groups and its use as a photosensitizer in dye-sensitized photoelectrochemical cells

Citation
E. Stathatos et al., Synthesis of a hemicyanine dye bearing two carboxylic groups and its use as a photosensitizer in dye-sensitized photoelectrochemical cells, CHEM MATER, 13(11), 2001, pp. 3888-3892
Citations number
22
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
CHEMISTRY OF MATERIALS
ISSN journal
08974756 → ACNP
Volume
13
Issue
11
Year of publication
2001
Pages
3888 - 3892
Database
ISI
SICI code
0897-4756(200111)13:11<3888:SOAHDB>2.0.ZU;2-R
Abstract
Two hemicyanine (aminostilbazium) dyes, one bearing two carboxylic groups w hile the other being its ester analogue, were synthesized for use as photos ensitizers in dye-sensitized photoelectrochemical cells (DSPEC). Only the d ye with carboxylic groups is covalently attached on mesoporous TiO2 films. The ester analogue, however, is physically adsorbed and it is easily washed off by several solvents. DSPECs of the Graetzel type, made of mesoporous T iO2 films (in our case, synthesized through the reverse-micellar route), of the aminostilbazium. bicarboxylate photosensitizer and of a I-/I-3(-)/prop ylenecarbonate electrolyte were tested and were found to yield more than 45 % maximum photon to electron conversion efficiency and 0.72% overall photov oltaic efficiency. The cells yielded a linear response within a wide range of illumination intensities.