Thieno[3,4-b]pyrazine as an Electron Deficient π-Bridge in D-A-π-A DSCs.
Liyanage NPDepartment of Chemistry and Biochemistry, University of Mississippi , University, Mississippi 38677, United States.
Yella ALaboratory of Photonics and Interfaces, Institution of Chemical Sciences and Engineering, School of Basic Sciences, Swiss Federal Institute of Technology , CH-1015, Lausanne, Switzerland.
Nazeeruddin MLaboratory of Photonics and Interfaces, Institution of Chemical Sciences and Engineering, School of Basic Sciences, Swiss Federal Institute of Technology , CH-1015, Lausanne, Switzerland.
Grätzel MLaboratory of Photonics and Interfaces, Institution of Chemical Sciences and Engineering, School of Basic Sciences, Swiss Federal Institute of Technology , CH-1015, Lausanne, Switzerland.
Delcamp JHDepartment of Chemistry and Biochemistry, University of Mississippi , University, Mississippi 38677, United States.
English
Thieno[3,4-b]pyrazine (TPz) is examined as an electron deficient π-bridge enabling near-infrared (NIR) spectral access in dye-sensitized solar cells (DSCs). Seven dissymmetric dyes for DSCs were synthesized (NL2-NL8) with TPz as the π-bridge utilizing palladium catalyzed C-H activation methodology. C-H bond cross-coupling was uniquely effective among the cross-couplings and electrophilic aromatic substitution reactions analyzed in monofunctionalizing the TPz building block. The TPz-based NL2-NL8 dyes examine the effects of various donors, π-spacers, and acceptors within the donor-π bridge-acceptor (D-π-A) dye design. Proaromatic TPz stabilizes the excited-state oxidation potential (E(s+/s*)) of the dyes by maintaining aromaticity upon excitation of the dye molecule. This leads to concise conjugated systems capable of accessing the NIR region. Through judicious structural modifications, dye band gaps were reduced to 1.48 eV, and power conversion efficiencies (PCEs) reached 7.1% in this first generation TPz-dye series.