Effect of Flank Rotation on the Photovoltaic Properties of Dithieno[2,3-:2',3'-']benzo[1,2-:4,5-']dithiophene-Based Narrow Band Gap Copolymers.

Side chain engineering has been an effective approach to modulate the solution processability, optoelectronic properties and miscibility of conjugated polymers (CPs) for organic/polymeric photovoltaic cells (PVCs). As compared with the most commonly used method of introducing alkyl chains, the employment of alkyl-substituted aryl flanks would provide two-dimensional (2-D) CPs having solution processability alongside additional merits like deepened highest occupied molecular orbital (HOMO) energy levels, increased absorption coefficient and charger transporting, etc. In this paper, the triple C≡C bond was used as conjugated linker to decrease the steric hindrance between the flanks of 4,5-didecylthien-2-yl (T) and dithieno[2,3-:2',3'-']benzo[1,2-:4,5-']dithiophene (DTBDT) core.