| Literature DB >> 25056642 |
Roberto Grisorio1, Luisa De Marco, Rita Agosta, Rosabianca Iacobellis, Roberto Giannuzzi, Michele Manca, Piero Mastrorilli, Giuseppe Gigli, Gian Paolo Suranna.
Abstract
This study deals with the synthesis and characterization of two π-extended organic sensitizers (G1 and G2) for applications in dye-sensitized solar cells. The materials are designed with a D-A-π-A structure constituted by i) a triarylamine group as the donor part, ii) a dithienyl-benzothiadiazole chromophore followed by iii) a further ethynylene-thiophene (G1) or ethynylene-benzene (G2) π-spacer and iv) a cyano-acrylic moiety as acceptor and anchoring part. An unusual structural extension of the π-bridge characterizes these structures. The so-configured sensitizers exhibit a broad absorption profile, the origin of which is supported by density functional theory. The absence of hypsochromic shifts as a consequence of deprotonation as well as notable optical and electrochemical stabilities are also observed. Concerning the performances in devices, electrochemical impedance spectroscopy indicates that the structural modification of the π-spacer mainly increases the electron lifetime of G2 with respect to G1. In devices, this feature translates into a superior power conversion efficiency of G2, reaching 8.1%. These results are comparable to those recorded for N719 and are higher with respect to literature congeners, supporting further structural engineering of the π-bridge extension in the search for better performing π-extended organic sensitizers.Entities:
Keywords: benzothiadiazole; dye sensitized solar cell; light-harvesting; structure-property relationship; π-extended organic sensitizer
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Year: 2014 PMID: 25056642 DOI: 10.1002/cssc.201402164
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928