The crystal structure, cohesive energy, and electronic properties of bulk phases of the fullerene derivative ͓6, 6͔-phenyl-C 61-butyric-acid-methyl-ester ͑PCBM͒ have been calculated using ab initio density-functional theory ͑DFT͒ techniques. We have only considered cubic and hexagonal crystal lattices with one PCBM molecule per primitive cell. It was found that the cohesive properties of these systems are determined mainly by two types of mechanisms, namely, the van der Waals interaction and the formation of weak hydrogen bonds. Among the considered crystal structures, the most stable one, which is also the most compact structure, is the simple cubic which has a cohesive energy difference of 1.27 eV with respect to the isolated PCBM molecule. Regarding the electronic properties, the simple-cubic PCBM crystal is found to be a semiconductor with an indirect band gap of 1.21 eV. In addition, we have also investigated the electronic contribution of the phenylbutyric-acid-methyl-ester tail to the electronic states of the entire system. By analyzing the projected density of states ͑DOS͒, we found that the states introduced by the tail are too far from the valence and conduction bands, so that the reduction of the band gap of bulk PCBM compared to PCBM molecule results only from the close packing. In addition, the tail introduces a splitting of the degenerate states of the molecule reducing the gap by about 0.2 eV compared to the C 60 molecule. On the other hand, it is shown that the simple hexagonal structure presents a layered structure with the separation between layers of 12.6 Å. Furthermore, in the cohesive curve, there is a nonvanishing cohesive energy for noninteracting layers. The study of the hexagonal monolayers shows a stable structure with a cohesive energy of 0.72 eV, which indicates that PCBM can form twodimensional systems when the PCBM molecules are deposited on the appropriate substrates. The results provided by this work may be important to improve our understanding concerning the mechanisms of formation of PCBM supramolecular structures, and how they can be modified to reach a desired particular property.

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Using transmission electron microscopy (TEM) and Z-contrast imaging we have demonstrated elongated nanostructure formation of fullerene derivative [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) within an organic host through annealing. The annealing provides an enhanced mobility of the PCBM molecules and, with good initial dispersion, allows for the formation of exaggerated grain growth within the polymer host. We have assembled these nanostructures within the regioregular conjugated polymer poly(3-hexylthiophene) (P3HT). This PCBM elongated nanostructure formation maybe responsible for the very high efficiencies observed, at very low loadings of PCBM (1:0.6, polymer to PCBM), in annealed photovoltaics. Moreover, our high resolution TEM and electron energy 2 loss spectroscopy studies clearly show that the PCBM crystals remain crystalline and are unaffected by the 200-keV electron beam.

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