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The emeraldine base (EB) form of polyaniline can be varied from insulating (o < 10-1°ohm-tcm l) to conducting (o-~ 10 + lohm-lcm -1) through protonation. That is, the number of electrons on the polymer backbone is constant while the number of protons is increased. We present here extensive magnetic, optical and transport data that demonstrate that the resulting emeraldine salt (ES) is metallic with axfinite density of states at the Fermi energy. The results are consistent with segregation into fully protonated emeraldine salt and unprotonated emeraldine base polymer regions. It is proposed that the observed transition is an isolated bipolaron-to-polaron lattice transition. The correspondence of this concept to the disproportionation between protonated imine plus amine to form two semiquinones is shown.

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In order to investigate the role of carbon nanotubes in a polymer matrix, organic light-emitting diodes were fabricated from a polymer composite composed of poly (m-phenylene vinylene-co-2,5-dioctoxy-p-phenylene) (PmPV) and dispersed single-wall carbon nanotubes (SWNTs). Tris-(8-hydroxyquinolinolato) aluminum (Alq3) doped by Nile Red was used as an emissive material between the polymer composite and cathode. The device fabricated without SWNTs dispersed in the PmPV shows a dominant emission near red at 600 nm, which is in the range of the characteristic emission of Nile Red-doped Alq3, with a small amount of green emission from the PmPV. However, the devices fabricated with the polymer composite show an increase in the oscillator strength of the green emission with a dominant emission peak near 500 nm, the characteristic emission of PmPV. This was observed for SWNT concentrations up to 0.1 wt %. The shift in the emission indicates that the SWNTs in the PmPV matrix act as a hole-blocking material that results in a shifting of the recombination region from the Nile Red-doped Alq3 layer to the PmPV composite layer.

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