Issue 4, 2006

Retardation of interfacial charge recombination by addition of quaternary ammonium cation and its application to low temperature processed dye-sensitized solar cells

Abstract

Electron lifetime (τ) in dye-sensitized solar cells (DSC), using electrolytes containing I/I3 redox couple, was investigated with quaternary ammonium cations having various alkyl chain lengths, and it was found that the lifetime increased in the order τTPAτTBA < τTHAτTHpA, where τTPA, τTBA, τTHA and τTHpA were the lifetimes with tetra-propyl, butyl, hexyl and heptyl ammonium cations respectively. On the other hand, little influence of the cations on electron diffusion coefficients was observed, indicating that the DSCs using these cations have longer electron diffusion length (L). New electrolyte compositions for DSCs were sought with THA+ to increase the lifetime and L without compromising charge injection yield from the dye to TiO2. The electrolyte was applied for DSCs using TiO2 electrode prepared by 150 °C sintering. Under one-sun conditions (100 mW cm−2), newly prepared electrolytes showed at most 40% increase of energy conversion efficiency in comparison to conventional electrolytes and the highest value was 4.7%, which was the highest among the reported values of low temperature processed DSCs. The increase of the efficiency was achieved by higher short-circuit current induced by longer electron diffusion length and higher open-circuit voltage due to higher electron density.

Graphical abstract: Retardation of interfacial charge recombination by addition of quaternary ammonium cation and its application to low temperature processed dye-sensitized solar cells

Article information

Article type
Paper
Submitted
12 Dec 2005
Accepted
09 Jan 2006
First published
01 Feb 2006

Photochem. Photobiol. Sci., 2006,5, 389-394

Retardation of interfacial charge recombination by addition of quaternary ammonium cation and its application to low temperature processed dye-sensitized solar cells

T. Kanzaki, S. Nakade, Y. Wada and S. Yanagida, Photochem. Photobiol. Sci., 2006, 5, 389 DOI: 10.1039/B517588G

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