Abstract
We report that exciton dissociation occurs within 150 fs during ultrafast photoexcitation at moderately high fluence, with $\ensuremath{\sim}10%$ quantum efficiency, in a model electroluminescent $\ensuremath{\pi}$-conjugated polymer. This is apparently inconsistent with the otherwise well-supported view that spin-singlet electron-hole pairs (excitons) are the primary photoexcitations. However, we demonstrate that resonant sequential transitions account quantitatively for the photoinduced polaron-pair yield, with the lowest ${(1B}_{u})$ exciton as an intermediate. Efficient exciton dissociation occurs either from the resulting high-energy, even-parity ${(A}_{g})$ states, or during ultrafast thermalization. The yield of photoinduced polarons, on the other hand, is $<0.1%$ under continuous-wave excitation, where access to high-energy states by sequential excitation is not significant.
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