Hybrid materials composed of n-doped fullerene/transition metal complex polymers and polypyrrole were formed under electrochemical or chemical conditions. The electrochemically synthesis, bilayers of both materials exhibit rectifying characteristics and can serve as a charge trapping system.
The core shell nanoparticles, i.e., poly-Pd3C60@polypyrrole (Figure 1), were prepared by sequential chemical polymerization of both components. These systems can be used for the modeling of the charge transfer processes in bulk-heterojunction solar devices. The outer polypyrrole layer is easily oxidized at potentials corresponding to the potentials of pure polypyrrole oxidation. The poly-Pd3C60 core reduction is shifted toward more negative potentials in comparison to the potential of reduction of pure poly-Pd3C60. The electrochemical measurements reveal that poly-Pd3C60@polypyrrole with outer polypyrrole layer doped with light harvesting molecules and thinner than about 20 nm can be potentially used in solar energy conversion electrochemical devices. The small thickness of the outer layer prevents free charge carriers recombination. The large area of p-n nanojunction in nanostructured material should increase efficiency of solar energy conversion. The electric charge formed at the p-n nanojunction can be also transferred from poly-Pd3C60inner sphere to the metallic collector.