Abstract

AbstractBoron subphthalocyanines (SubPcs) are attractive as light harvesting materials in photovoltaic devices. Here we present the synthesis, optical and electrochemical properties, and device performances of a series of donor−acceptor‐functionalized SubPc derivatives incorporating a carboxylic acid for anchoring onto TiO2. Liquid‐ and solid‐state dye‐sensitized solar cells (DSCs) were prepared from three compounds, and a triad system consisting of two aniline donor moieties and a benzothiadiazole acceptor moiety was found to exhibit the highest power conversion efficiency (PCE) in the series (PCE=1.54 %; solid‐state device). The compounds were prepared by stepwise acetylenic coupling reactions. In addition, we present the synthesis and optical properties of a SubPc derivative incorporating three anilino‐substituted 1,1,4,4‐tetracyanobutadiene units, prepared by the [2+2] cycloaddition between three ethynyl units at the SubPc periphery and three tetracyanoethylene molecules followed by electrocyclic ring‐opening reactions.

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