Electric field assisted charge carrier photogeneration in poly(spirobifluorene-co-benzothiadiazole).

The dynamics of charge carrier generation in poly(spirobifluorene-co-benzothiadiazole) was investigated by electric field-induced fluorescence quenching and differential absorption measurements. Three different time domains of carrier generation have been identified: an ultrafast phase, a subnanosecond phase, and an entire lifetime phase. The charge generation efficiencies during the first and second phases were found to be almost independent of temperature, being about 25% and 10%, respectively, at an applied electric field of 1.3×10(6) V/cm, while the generation efficiency during the third phase increases from 2% at 80 K to 10% at room temperature. The results of transient spectroscopy measurements and quantum chemical calculations suggest an intramolecular charge transfer for about 1 ps from the alkoxy-substituted fluorene side group to the benzothiadiazole subunit of the main chain. The formation and evolution of the resulting charge transfer states determine the way of charge carrier generation.

Ultrafast dynamics of carrier mobility in a conjugated polymer probed at molecular and microscopic length scales.

We used time-resolved electric-field-induced second-harmonic generation to probe the charge-carrier-mobility dynamics in amorphous organic materials on an ultrafast time scale. We were able to show that the mobility in poly-spiro-bifluorene-co-benzothiadiazol decreases from 0.1 cm 2/V s at 1 ps to 10-6 cm2/V s within 1 mus. We attribute this dramatic decrease to the relaxation of the charge carriers within the density of states, clearly demonstrating the impact of disorder on the nanoscale charge transport in amorphous semiconductors.