Pseudo-doping effect on structural and electrical properties of polyaniline-camphorsulfonic acid
Fábio F. F. Garrudo, L.F. Vieira Ferreira, Ana M. Ferraria, A.M. Botelho do Rego, Ana Charas, Vânia André, M. Teresa Duarte, Robert J. Linhardt, Frederico Castelo Ferreira, Jorge Morgado
Abstract
Electroconductive polymers (ECP) are critical for the design of soft electronic and bioelectronic devices. Polyaniline:camphorsulfonic acid (PANI:CSA) is an example of a biocompatible and affordable ECP, whose electroconductivity is highly dependent on chain organization/conformation. PANI:CSA aggregation ordering is overlooked in most works, but it can greatly impact the performance of PANI:CSA-based devices and limit their applicability. A simple and cheap method to avoid random coil aggregation of PANI:CSA is to select solvents with pseudo-doping properties. This work presents a novel alternative solvent system, based on trifluoroethanol (TFE) and hexafluoropropanol (HFP) mixtures, capable of being removed without hampering the structural and electrical properties of PANI:CSA. For the first time, we present a systematic study that compares the performance of solvent systems containing different amounts of TFE and HFP, which, unlike m-cresol, the golden-standard of pseudo-doping, are easy to remove without compromising the ECP’s electroconductivity and biocompatibility. We also evaluate the influence of the processing method, drop-casting vs spin-coating, on the structural and electrical properties of the obtained samples. Samples obtained by spin-coating show a more consistent improvement in electroconductivity (σ(TFE) = 61 S cm-1, σ(TFE:HFP (50:50 vol)) = 70 S cm-1) and more intense near-infrared (NIR) absorption bands. Atomic force microscopy (AFM), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) indicate that samples processed with HFP and m-cresol have higher benzenoid content, lower random coil aggregation and more efficient CSA doping. The solvent system comprised of equal parts of TFE and HFP was found to simultaneously enhance the electrical properties and structural ordering of PANI:CSA. We believe our results are critical for the fabrication of PANI-based next generation bioelectronic devices.