4.5 Article

Unsymmetrical squarylium dyes with π-extended heterocyclic components and their application to organic dye-sensitized solar cells

Journal

SYNTHETIC METALS
Volume 161, Issue 21-22, Pages 2481-2487

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.synthmet.2011.09.035

Keywords

Squarylium dye; Near-infrared; Dye-sensitized solar cells; Nanocrystalline TiO(2)

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan [22750180]
  2. Inamori Foundation
  3. Grants-in-Aid for Scientific Research [22750180] Funding Source: KAKEN

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Novel pi-extended squarylium dyes have been synthesized as sensitizers for use in dye-sensitized solar cells (DSSCs). Four quaternary salts with extended pi-systems, quinolinium, benz[c,d]indolium, benzopyrylium, and benzo-1-thiopyrylium, were selected as electron-rich heterocyclic components and condensed with indole-based semisquarylium bearing a carboxyl group as an anchor for their immobilization on TiO(2) to obtain four unsymmetrical squarylium dyes (SQ1-4). They exhibited intense absorption in the near-infrared region in solution and on the TiO(2) surface (absorption edge: approximately 900 nm). Investigation of their electrochemical properties revealed that electron injection from the excited dyes to the TiO(2) conduction band was thermodynamically permitted. A molecular-orbital calculation indicated that the electron distribution moved from the cyclobutene core to the heterocyclic components bearing the carboxyl group by photoexcitation of SQ1-4. The photovoltaic performances of DSSCs based on the squarylium dyes significantly depended on the structure of heterocyclic components. Among the series of squarylium dyes, SQ2-4 achieved comparatively high performance in metal-free NIR sensitizers (eta = 1.1-1.6%), in accordance with the calculation results. These results suggest that the structure of heterocyclic components strongly affects not only the absorption properties of the dyes but also the photovoltaic performances of DSSCs based on these dyes. (C) 2011 Elsevier B.V. All rights reserved.

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