Structural, optical and electrochemical properties of reduced graphene oxide-polyaniline composites for supercapacitor applications

In the present work, polyaniline-reduced graphene oxide (PANI-rGO) nanocomposite films were synthesized by varying their concentration in composites of rGO nanosheets, and ammonium sulfate (NH 4 ) 2 SO 4 was used as a catalyst. The microstructural, structural network, optical, compositional, and ele...

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Veröffentlicht in:Journal of materials science. Materials in electronics 2024-11, Vol.35 (31), p.2037, Article 2037
Hauptverfasser: Mustafa, Zeeshan, Kumar, Dhruva, Pradhan, B. B., Swain, Bibhu Prasad, Ghadai, Ranjan Kumar
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Sprache:eng
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Zusammenfassung:In the present work, polyaniline-reduced graphene oxide (PANI-rGO) nanocomposite films were synthesized by varying their concentration in composites of rGO nanosheets, and ammonium sulfate (NH 4 ) 2 SO 4 was used as a catalyst. The microstructural, structural network, optical, compositional, and electrochemical properties of rGO/PANI nanocomposites were investigated using scanning electron microscopy X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), UV–Vis spectroscopy, X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CV). The XRD peaks obtained for both PANI and G/PANI Nanocomposite at 14.5 ◦ , 19.87 ◦ , and 25.6 ◦ , with the corresponding planes of (011), (020), and (200), confirm the successful synthesis of both PANI and G/PANI nanocomposites, resulting in a more ordered structure with high crystallinity during polymerization. FTIR, UV–Vis, and Raman spectroscopy results show that strong π − π interactions aided in the uniform distribution of PANI on the rGO nanosheets. Furthermore, the XPS results demonstrate the presence of C-H, N–H, C–C, and C-O bonds, corroborating the FTIR and Raman spectroscopy findings. The electrochemical properties of the PANI-rGO confirm its possible applications as a promising electrode material for high-performance supercapacitors.
ISSN:0957-4522
1573-482X
DOI:10.1007/s10854-024-13806-8