TY - JOUR
T1 - Donor−Acceptor-Functionalized Subphthalocyanines for Dye-Sensitized Solar Cells
AU - Gotfredsen, Henrik
AU - Neumann, Timo
AU - Storm, Freja Eilsø
AU - Muñoz, Alberto Viñas
AU - Jevric, Martyn
AU - Hammerich, Ole
AU - Mikkelsen, Kurt V.
AU - Freitag, Marina
AU - Boschloo, Gerrit
AU - Nielsen, Mogens Brøndsted
PY - 2018/11/1
Y1 - 2018/11/1
N2 - Boron 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.
AB - Boron 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.
U2 - 10.1002/cptc.201800135
DO - 10.1002/cptc.201800135
M3 - Journal article
SN - 2367-0932
VL - 2
SP - 976
EP - 985
JO - ChemPhotoChem
JF - ChemPhotoChem
IS - 11
ER -