4.4 Article

Synthetic analogues of anthocyanins as sensitizers for dye-sensitized solar cells

Journal

PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES
Volume 12, Issue 5, Pages 883-894

Publisher

SPRINGERNATURE
DOI: 10.1039/c3pp25347c

Keywords

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Funding

  1. EFOR Project
  2. CNR
  3. Project SAGRO
  4. Regione Siciliana (Assessorato Regionale Attivita Produttive progetti PO FESR linea d'intervento) [4.1.1.1]
  5. Fundacao para a Ciencia e Tecnologia through the National Portuguese NMR Network [C/EQB/LA0006/2011, PTDC/QUI-QUI/119932/2010]
  6. Programma Operativo Nazionale Ricerca e Competitivita [PON 01_02257 FOTORIDUCO2]
  7. Fundação para a Ciência e a Tecnologia [PTDC/QUI-QUI/119932/2010] Funding Source: FCT

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Seven flavylium salt dyes were employed for the first time as sensitizers for dye-sensitized solar cells (DSSCs). The theoretical and experimental wavelengths of the maximum absorbances, the HOMO and LUMO energy levels, the coefficients, the oscillator strengths and the dipole moments are calculated for these synthetic dyes. The introduction of a donor group in the flavylium molecular structure was investigated. Photophysical and photoelectrochemical measurements showed that some of these synthetic analogues of anthocyanins are very promising for DSSC applications. The best performance was obtained by a DSSC based on the novel compound 7-(N,N-diethylamino)-3',4'-dihydroxyflavylium which produced a 2.15% solar energy-to-electricity conversion efficiency, under AM 1.5 irradiation (100 mW cm(-2)) with a short-circuit current density (J(sc)) of 12.0 mA cm(-2), a fill factor of 0.5 and an open-circuit voltage (V-oc) of 0.355 V; its incident photocurrent efficiency of 51% at the peak of the visible absorption band of the dye is remarkable. Our results demonstrated that the substitution of a hydroxylic group with a diethylamine unit in position 7 of ring A of the flavylium backbone expanded the pi-conjugation in the dye and thus resulted in a higher absorption in the visible region and is advantageous for effective electron injection from the dye into the conduction band of TiO2.

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