Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
175567 | Dyes and Pigments | 2015 | 7 Pages |
•Tetraindole-based organic dyes have been synthesized for the first time.•The saddle-shaped structure is favourable for suppressing the dye aggregation.•The dye with a bithiophene as the π-bridge exhibited better performances.•An efficiency up to 6.46% has been achieved with a high Voc of 762 mV.
Two new metal-free organic dyes which consist of a saddle-shaped tetraindole donor, a cyanoacrylic acid acceptor/anchoring group and a thiophene or bithiophene π-bridge have been successfully designed and synthesized for dye-sensitized solar cells. The two dyes showed good photoelectric properties, and the saddle-shaped structure of the tetraindole unit was found to be favorable for preventing intermolecular aggregation and enhancing the photovoltage. The two tetraindole-based dyes exhibited good photovoltaic performances in solar cells. An efficiency up to 6.46% with a high open-circuit photovoltage of 762 mV was achieved for the dye JY15 with a 2,2′-bithiophene moiety as the π-bridge using an iodine electrolyte under standard conditions.
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