Abstract
Uncovering the precise effect of the conjugated polymer chain length on the semiconducting properties in thin-film devices is confounded by the step-growth polymerization techniques typically used. Here, we use preparatory size exclusion chromatography to isolate fractions of two diketopyrrolopyrrole-thiophene based co-polymers with low molar-mass dispersity, ĐM, and number average molecular weights up to 180 kDa. We find that the charge carrier mobility can vary over three orders of magnitude in the range from 9 to 70 kDa, while a factor of 3–4 increase in photovoltaic performance was noted over the same range. The effect of ĐM was found to be most drastic when the largest chains were mixed with the shortest. The study of the thin-film morphology and crystallinity by GIWAXS give further insights into the origin of these effects. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016
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