4.6 Article

Adamantyl Side Chains as Anti-Aggregating Moieties in Dyes for Dye-Sensitized Solar Cells

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 28, Issue 51, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202201726

Keywords

adamantane; anti-aggregation; anti-recombination; dye design; dye-sensitized solar cells; triarylamine dye

Funding

  1. Research Council of Norway [226244/F50, 245963/F50]

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A novel concept of tethering an anti-aggregation unit to dyes for dye-sensitized solar cells (DSSCs) was introduced. The study demonstrates the successful increase in photovoltages in devices employing copper-based electrolytes by decorating the donor dye with a steric ethyladamantyl moiety. The best photovoltaic performance was achieved by combining the adamantyl decorated donor dye with CDCA, showcasing the potential of ethyladamantyl side chains for surface protection of TiO2.
Designing and evaluating novel dye concepts is crucial for the development of the field of dye-sensitized solar cells (DSSCs). In our recent report, the novel concept of tethering the anti-aggregation additive chenodeoxycholic acid (CDCA) to dyes for DSSC was introduced. Based on the performance improvements seen for this modification, the aim of this study is to see if a simplified anti-aggregation unit could achieve similar results. The following study reports the synthesis and photovoltaic characterization of two novel dyes decorated with the steric ethyladamantyl moiety on the pi-spacer, and on the triarylamine donor. This modification is demonstrated to be successful in increasing the photovoltages in devices employing copper-based electrolytes compared to the non-modified reference dye. The best photovoltaic performance is achieved by a device prepared with the adamantyl decorated donor dye and CDCA, this device achieves a power conversion efficiency of 6.1 % (Short-circuit current=8.3 mA cm(-2), Open-circuit voltage=1054 mV, Fill factor=0.69). The improved photovoltaic performance seen for the adamantyl decorated donor demonstrate the potential of ethyladamantyl side chains as a tool to ensure surface protection of TiO2.

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