4.6 Article

Development of D-pi-Cat fluorescent dyes with a catechol group for dye-sensitized solar cells based on dye-to-TiO2 charge transfer

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 2, Issue 22, Pages 8500-8511

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ta01286k

Keywords

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Funding

  1. Japan Society for the Promotion of Science (JSPS) [24550225]
  2. Tokuyama Science Foundation

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D-pi-Cat fluorescent dyes YM-1 and YM-2 with a diphenylamine moiety as the electron-donating group, a catechol (Cat) unit as the anchoring group and fluorene or carbazole as the pi-conjugated system were designed and developed as a photosensitizer for type-II dye-sensitized solar cells (DSSCs), which have a direct electron-injection pathway from the dye to the conduction band (CB) of the TiO2 electrode by photoexcitation of the dye-to-TiO2 charge transfer (DTCT) bands. Furthermore, not only to gain insight into the influence of the molecular structure of D-pi-Cat dyes on the appearance of a DTCT band and the electron-injection mechanism, but also to investigate the impacts of the DTCT characteristics of D-pi-Cat dyes on the photovoltaic performances of DSSCs, a D-pi-Cat fluorescent dye YM-3 with carbazole-terthiophene as the pi-conjugated system was also synthesized. It was found that the D-pi-Cat dyes possess a good light-harvesting efficiency (LHE) in the visible region due to a broad absorption band corresponding to DTCT upon binding to a TiO2 film. The incident photon-to-current conversion efficiency (IPCE) corresponding to the DTCT band for DSSCs based on YM-1 and YM-2 is higher than that for YM-3. This work indicates that the stabilization of the LUMO level and the expansion of the pi-conjugated system by the introduction of a long pi-bridge such as terthiophene on the Cat moiety can lead to an increase in the intramolecular charge transfer (ICT) excitation based on pi -> pi* transition with a decrease in the DTCT characteristics, resulting in enhancement of an indirect electron-injection pathway from the excited dye to the CB of TiO2 by photoexcitation of the local band of the adsorbed dye on TiO2.

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