4.6 Article

Synthesis, optical, electrochemical and photovoltaic properties of a D-pi-A fluorescent dye with triazine ring as electron-withdrawing anchoring group for dye-sensitized solar cells

Journal

RSC ADVANCES
Volume 5, Issue 27, Pages 21012-21018

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra16399k

Keywords

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Funding

  1. Iwatani Naoji Foundation's Research Grant

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The D-pi-A fluorescent dye OUJ-1 with 1,3,5-triazine ring as electron-withdrawing anchoring group and (diphenylamino) carbazole containing a thiophene ring as D-pi moiety have been newly developed and their optical and electrochemical properties, adsorption states on TiO2 nanoparticles, and photovoltaic performance in dye-sensitized solar cell (DSSC) were investigated. The absorption maximum (lambda(abs)(max)) for the intramolecular charge-transfer (ICT) absorption band of the D-pi-A dye OUJ-1 occurs at a longer wavelength than those of D-pi-A dye NI-6 with a pyridyl group and D-pi-A dye OUK-1 with a pyrzayl group. Moreover, the dye OUJ-1 exhibits significant fluorescence solvatochromic properties, that is, a bathochromic shift of the fluorescence band and a decrease in the fluorescence quantum yield (Phi) due to a change from the (ICT)-I-1 excited state to the twisted intramolecular charge transfer (TICT) excited state with increasing solvent polarity were observed. The photovoltaic performance of a DSSC based on OUJ-1 is lower than those of NI-6 and OUK-1 due to the low dye loading of OUJ-1 on TiO2 electrode. It was found that the dye OUJ-1 is adsorbed onto the TiO2 surface through the formation of trizainium ions at the Bronsted acid sites (surface-bound hydroxyl groups, Ti-OH) on the TiO2 surface, although the dye NI-6 was predominantly adsorbed on the TiO2 through coordinate bonding between the pyridyl group of the dye and the Lewis acid sites (exposed Tin+ cations) on the TiO2 surface, and the dye OUK-1 was adsorbed on the TiO2 surface through both the formations of hydrogen bonding of pyrazyl groups and pyrazinium ions at Bronsted acid sites on the TiO2 surface. This work revealed that the binding mode of D-pi-A dye sensitizers with azine rings on the TiO2 surface can be changed by control of the basicity and electron density of the azine rings.

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