An Aqueous Exfoliation of WO3 as a Route for Counterions Fabrication—Improved Photocatalytic and Capacitive Properties of Polyaniline/WO3Composite

Abstract

In this paper, we demonstrate a novel, electrochemical route of polyaniline/tungsten oxide (PANI)/WO3) film preparation. Polyaniline composite film was electrodeposited on the FTO (fluorine-doped tin oxide) substrate from the aqueous electrolyte that contained aniline (monomer) and exfoliated WO3 as a source of counter ions. The chemical nature of WO3 incorporated in the polyaniline matrix was investigated using X-ray photoelectron spectroscopy. SEM (scanning electron microscopy) showed the impact of WO3 presence on the morphology of polyaniline film. PANI/WO3 film was tested as an electrode material in an acidic electrolyte. Performed measurements showed the electroactivity of both components and enhanced electrochemical stability of PANI/WO3 in comparison with PANI/Cl. Thus, PANI/WO3 electrodes were utilized to construct the symmetric supercapacitors. The impact of capacitive and diffusion-controlled processes on the mechanism of electrical energy storage was quantitatively determined. Devices exhibited high electrochemical capacity of 135 mF cm−2 (180 F g−1) and satisfactory retention rate of 70% after 10,000 cycles. The electrochemical energy storage device exhibited 1075.6 W kg−1 of power density and 12.25 Wh kg−1 of energy density. We also investigated the photocatalytic performance of the deposited film. Photodegradation efficiencies of methylene blue and methyl orange using PANI/WO3 and PANI/Cl were compared. The mechanism of dye degradation using WO3-containing films was investigated in the presence of scavengers. Significantly higher efficiency of photodecomposition of dyes was achieved for composite films (84% and 86%) in comparison with PANI/Cl (32% and 39%) for methylene blue and methyl orange, respectively.

The valance state of vanadium-key factor in the flexibility of potassium vanadates structure as cathode materials in Li-ion batteries

“…The total current response of an electrode is a mixture of these mechanisms: where k 1 ·v is the capacitance related process while k 2 ·v 1/2 is attributed to diffusion-controlled mechanism. One should take into account that in a real system simple mechanism does not occur 48 . To evaluate the charge storage contribution the analysis of the sweep-rate of voltammetric currents was performed, see Fig.…”