Abstract
Poly (3-hexylthiophene) (P3HT) was an early frontrunner in the development of donor polymers to be used in organic photovoltaics. A relatively straightforward and inexpensive synthesis suggests that it may be the most viable donor polymer to use in large-scale commercial organic solar cells. Replacing fullerenes with new electron acceptors has led to significant improvements in device performance and stability, with devices now able to exceed an efficiency of 7%. Past studies have reported a dependence of device performance on the molecular weight of the polymer in fullerene-containing blends, however, with nonfullerene acceptors now showing promise a similar study was needed. P3HT blends, with two nonfullerene acceptors (O-IDTBR and EH-IDTBR), were probed using a number of polymer batches with varying molecular weights. O-IDTBR was shown to exhibit a dependence on the polymer molecular weight, with optimal performance achieved with a 34 kDa polymer, while EH-IDTBR displayed an independence in performance with varying polymer molecular weight. Probing the thermal and morphological behavior of the P3HT:O-IDTBR blends suggests that an optimal morphology with pronounced donor and acceptor domains was only achieved with the 34 kDa polymer, and a greater degree of mixing was exhibited in the other blends, likely leading to poorer device performance.