@article{oai:nagoya.repo.nii.ac.jp:00024033,
 author = {Kimura, Yuki and Maeda, Takeshi and Iuchi, Satoru and Koga, Nobuaki and Murata, Yasujiro and Wakamiya, Atsushi and Yoshida, Kumi},
 journal = {Journal of Photochemistry and Photobiology A: Chemistry},
 month = {Feb},
 note = {Five anthocyanins, namely, pelargonidin, cyanidin, delphinidin, petunidin and malvidin 3-O-glucosides, possessing different substitution patterns in the B-ring of the anthocyanidin chromophore were isolated from various plant materials. Dye-sensitized solar cells (DSSCs) were fabricated using the pure pigments, and then their cell colors and conversion efficiencies (η%) were compared. After optimization of the fabrication conditions, all the cells showed 0.6–1.4% conversion efficiency under AM 1.5. Among them, petunidin 3-O-glucoside provided the highest efficiency of 1.42% following the addition of deoxycholic acid (DCA) as an additive; however, removal of the glucosyl unit decreased the efficiency. The cell colors of cyanidin, delphinidin, and petunidin 3-O-glucosides appeared bluer with relatively high η% (>1%) values compared with those of pelargonidin and malvidin 3-O-glucosides. These phenomena may indicate that the former three pigments may attach to TiO2 through the catechol moiety of the B-ring of the chromophores. Time-dependent density functional theory (TD-DFT) calculations were performed on model systems consisting of anthocyanidin dyes on a (TiO2)38 cluster to characterize the photo-absorption properties of DSSCs.},
 pages = {230--238},
 title = {Characterization of dye-sensitized solar cells using five pure anthocyanidin 3-O-glucosides possessing different chromophores},
 volume = {335},
 year = {2017}
}