Influence of benzimidazole additives in electrolytic solution on dye-sensitized solar cell performance was written by Kusama, Hitoshi;Arakawa, Hironori. And the article was included in Journal of Photochemistry and Photobiology, A: Chemistry in 2004.Related Products of 3012-80-4 This article mentions the following:
The influence of benzimidazole additives on the performance of a bis(tetrabutylammonium)-cis-bis(thiocyanato)bis(2,2′-bipyridine-4-carboxylic acid, 4′-carboxylate)ruthenium(II) dye-sensitized TiO2 solar cell with an I–/I3– redox electrolyte in acetonitrile was studied by measuring the current-voltage characteristics of >20 different benzimidazole derivatives under AM 1.5 (100 mW/cm2). The benzimidazole additives tested had varying effects on the cell performance. Adding benzimidazole drastically enhanced the open-circuit photovoltage (Voc) and the fill factor (ff), but reduced the short-circuit photocurrent d. (Jsc) of the solar cell. To determine the reasons for the additive effects on cell performance the phys. and chem. properties of the benzimidazoles were computationally calculated Consequently, the greater the calculated partial charge of the nitrogen atoms in position 3 of the benzimidazole groups, the larger the Voc, but the smaller the Jsc values. The Voc values also increased as the mol. size of the benzimidazole derivatives decreased. Also, the greater the absolute difference between the calculated dipole moment of the benzimidazole and acetonitrile, the larger the Jsc value. Probably these properties of the benzimidazoles influenced the extent of interaction between the TiO2 electrode and electrolyte solvent, which changed the dye-sensitized solar cell performance. In the experiment, the researchers used many compounds, for example, 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde (cas: 3012-80-4Related Products of 3012-80-4).
1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde (cas: 3012-80-4) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Related Products of 3012-80-4
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem