Charge separation and fullerene triplet formation in blend films of polyfluorene polymers with [6,6]-phenyl C61 butyric acid methyl ester.

Transient and steady state optical spectroscopies were used to study thin films made from a series of polyfluorene polymers blended with [6,6]-phenyl C61 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 DeltaE(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 DeltaE(CS) is greater than this threshold, PCBM triplet formation is observed in preference to charge pair generation. If DeltaE(CS) 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 DeltaE(CS) is found to be similar to the PCBM singlet energy.

Long-lived exciplex formation and delayed exciton emission in bulk heterojunction blends of silole derivative and polyfluorene copolymer: the role of morphology on exciplex formation and charge separation.

Long-lived exciplex emission is observed in blend films of poly[9,9-dioctylfluorene-co-N-(4-methoxy-phenyl)diphenylamine] (TFMO) and the soluble silole derivative 2,5-bis-(2,2-bipyridin-6-yl)-1,1-dimethyl-3,4-diphenylsilacyclopentadiene (PyPySPyPy). The exciplex is characterized by a long-lived (approximately 40-90 ns) component in both the photoluminescence and electroluminescence spectra, which is red-shifted relative to the emission of the pristine materials. In addition to exciplex emission, delayed fluorescence from the TFMO singlet state is observed and is attributed to exciton regeneration through the interfacial exciplex state. Comparing blend films made using chlorobenzene and p-xylene solvents, we find that exciplex lifetime and exciton regeneration in the blend film are sensitive to the choice of solvent and the resulting morphology of the blend film. The exciplex emissive lifetime can be correlated to changes in photoluminescence quenching and efficiency of light-emitting diodes.

Device Performance of APFO-3/PCBM Solar Cells with Controlled Morphology.

Polymer/fullerene solar cells with three different device structures: A) diffuse bilayer, B) spontaneously formed multilayer, and C) vertically homogenous thin films, are fabricated. The photocurrent/voltage performance is compared and it is found that the self-stratified structure (B) yields the highest energy conversion efficiency.