This analysis discovers how varying graphene oxide sizes influence polyaniline synthesis in electrochemical applications, indicating potential for advanced material designs.
In this work, the effect of aqueous dispersions of graphene oxide (GO) and nanosized graphene oxide (nGO) on the enzymatic polymerization of polyaniline (PANI) was studied. The enzymatic polymerization of PANI was carried out in aqueous medium using toluenesulfonic acid (TSA) as the dopant, horseradish peroxidase (HRP) as the catalyst, and hydrogen peroxide (H2O2) as the oxidant, using 1.0, 2.5, and 5.0 wt% of GO and nGO. The morphology of PANI-GO/nGO composites was studied by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Further characterization was performed by thermogravimetric analysis (TGA) and spectroscopic techniques such as ultraviolet–visible (UV–Vis), Fourier-transform infrared (FTIR), Raman and X-ray photoelectronics (XPS). SEM images showed that during enzymatic polymerization, PANI completely covers the GO/nGO sheets. Furthermore, physicochemical results confirmed the production of a hybrid PANI-GO/nGO material with Van der Waals-type interactions between the oxygen-based functional groups of GO and the secondary amino bond (-NH-) of PANI. Also, cyclic voltammetry experiments were carried out in situ during the polymerization of PANI-GO/nGO films. The electrochemical response of PANI-GO/nGO composites reflects two broad oxidation peaks around 300 mV and 500 mV during anodic scanning, with reversible oxidation during cathodic scanning. Classical molecular dynamics simulations were used to understand the mechanism of the composite film’s growth.
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Guerrero-Bermea et al. (2025) studied this question.
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