In recent years the use of solvent additives for fabrication of polymer-based solar cells has become an important procedure to induce morphological changes at the system nanoscale, a critical step to improve device performance. Yet the actual effects of those additives on the polymer’s backbone conformations (with coupled variations on the electronic structure) remain very elusive. By combining different experimental and theoretical techniques, we show that the use of the solvent additive 1,8-diiodooctane (DIO) might influence the conformation of poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-bithiophene] (F8T2) chains resulting in improved properties of the film. We correlate this conformational variation with the photovoltaic response of F8T2:fullerene(C60) devices prepared using different DIO concentrations. We find that the efficiency of the devices increases more than 100%, and the hole mobility in the F8T2 films increases almost 1 order of magnitude with the use of DIO. A comparison between experimental data and the properties of the calculated structures suggests that the additive induces a higher density of syn conformers in the bithiophene unit of the copolymer backbone, planarizing the polymer’s geometry. The simulations indicate that this transition is very likely mediated by the electrostatic interaction between the iodine atom of the DIO and the heteroatoms of the bithiophene moiety. The higher degree of electronic delocalization and the enhancement of the interchain interactions improve the transport and the photovoltaic features of F8T2 layers. The use of solvent additive treatments to control conformational variations of the backbone might be a promising strategy to improve the optoelectronic properties of polymer-based devices.
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