Abstract
Transient and steady state optical spectroscopies were used to study thin films made from a series of polyfluorene polymers blended with [6,6]-phenyl C-61 butyric acid methyl ester (PCBM) in order to determine the influence of polymer ionisation potential on photoinduced charge separation. We find that the energy of the charge separated state Delta E-CS, given by the energy difference between the ionisation potential of the polymer and the electron affinity of the fullerene, must be smaller than a threshold value of about 1.6 eV for charge separation to occur. When Delta E-CS is greater than this threshold, PCBM triplet formation is observed in preference to charge pair generation. If DECS is similar to the threshold value, both PCBM triplet formation and charge separation occur in the blend film, with a tendency for charge separation to dominate over PCBM triplet formation as PCBM concentration increases. The mechanism of triplet formation is believed to be energy transfer to the PCBM singlet state followed by intersystem crossing. The threshold value of Delta E-CS is found to be similar to the PCBM singlet energy.