Small D–π–A Systems with o‐Phenylene‐Bridged Accepting Units as Active Materials for Organic Photovoltaics |
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Authors: | Dr. Antoine Leliège M. Sc. Jérémie Grolleau M. Sc. Magali Allain Dr. Philippe Blanchard Dr. Dora Demeter Dr. Théodulf Rousseau Dr. Jean Roncali |
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Affiliation: | LUNAM, University of Angers, CNRS UMR 6200, MOLTECH‐Anjou, Linear Conjugated Systems Group, 2 Bd Lavoisier, 49045 Angers (France) |
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Abstract: | Donor–acceptor (D–π–A) systems that combine triarylamine donor blocks and dicyanovinyl (DCV) acceptor groups have been synthesized. Starting from the triphenylamine (TPA)? thiophene? DCV compound ( 1 ) as a reference system, various synthetic approaches have been developed for controlling the light‐harvesting properties and energy levels of the frontier orbitals in this molecule. Thus, the introduction of methoxy groups onto TPA, the replacement of one phenyl ring of TPA by a thiophene ring, or the extension of the π‐conjugating spacer group lead to the modulation of the HOMO level. On the other hand, the fusion of the DCV group onto the vicinal thiophene ring by an ortho‐phenylene bridge allows for a specific fine‐tuning of the LUMO level. The electronic properties of the molecules were analyzed by using UV/Vis spectroscopy and cyclic voltammetry and the compounds were evaluated as donor materials in basic bilayer planar heterojunction solar cells by using C60 as acceptor material. The relationships between the electronic properties of the donors and the performance of the corresponding photovoltaic devices are discussed. Bilayer planar heterojunction solar cells that used reference compound 1 and C70 afforded power‐conversion efficiencies of up to 3.7 %. |
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Keywords: | bridging ligands chromophores cyclic voltammetry donor– acceptor systems solar cells |
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