Doping-Induced Conductivity Transitions in Molecular Layers of Polyaniline: Detailed Structural Study

We report detailed structural investigations, by synchrotron X-ray reflectivity (XRR), grazing incidence diffraction (GID), and space-resolved grazing incidence X-ray-induced fluorescence (GIXF), on the structure of molecular layers of polyaniline (PANI) that can be converted from insulating to conducting state simply by doping. We first address the simpler, but more intriguing, system, i.e., a floating monolayer of PANI on different subphases, for which we found a typical thickness of 28(1) angstrom, not much affected by the doping process. For the doped film we also found all internal lateral structure, with in-plane spacing of 3.5 angstrom-albeit with a small coherence of 3-4 repeat units only-compatible with face-to-face interchain stacking of phenyl rings, in agreement with the literature. By GIXF we could confirm the crucial role of Cl(-) intercalation in the doping process of the PANI film: under doping conditions (0.1 M HCl subphase) the Cl(-) intake is 8 times larger than in nondoping conditions (0.1 M KCl subphase). Multilayers transferred onto solid substrate were studied also as a function of the applied voltage, as this system constitutes the core of an electrochemically controlled device whose strongly nonlinear characteristic make it useful for applications to adaptive networks for complex information processing. By the application of all electrostatic field of 140 V/m, Cl ionic migration was observed confined to the polymeric film surface.