Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
177152 | Dyes and Pigments | 2011 | 7 Pages |
An acetylene-linked porphyrin-perylene anhydride and an acetylene-linked porphyrin-naphthalic anhydride have been synthesized; the highly conjugated acetylenic bridge in these porpyrins efficiently mediates electronic interaction between the porphyrin and perylene units to extend the π-conjugation of the porphyrin dye and to cause both broadening and red shifts of both the Soret and Q absorption bands. This condition is a useful feature for efficient dye-sensitized solar cell applications. The optical, electrochemical and photovoltaic properties of the new linked anhydrides show that the HOMO–LUMO gap decreased upon extension of π-conjugation, indicating a strong electronic coupling between the porphyrin and the perylene or naphthalene unit.
► An acetylene-linked porphyrin-perylene anhydride and an acetylene-linked porphyrin-naphthalic anhydride behave as sensitizers. ► A strong electronic coupling exists between the porphyrin and the linker. ► The extended π-conjugation improves the light-harvesting capability of porphyrin dyes.