Synthesis and supercapacitor performance of polyaniline-titanium dioxide-samarium oxide (PANI/TiO2-Sm2O3) nanocomposite
TiO 2 -Sm 2 O 3 binary oxide has been successfully synthesized using a two steps photolysis method with UV-irradiation (15 W and 256 nm) as a power source of irradiation system, and it modified PANI during simple oxidative polymerization route to get polyaniline/Sm 2 O 3 -TiO 2 nanocomposite. The st...
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Veröffentlicht in: | Chemical papers 2022-03, Vol.76 (3), p.1401-1412 |
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Sprache: | eng |
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Zusammenfassung: | TiO
2
-Sm
2
O
3
binary oxide has been successfully synthesized using a two steps photolysis method with UV-irradiation (15 W and 256 nm) as a power source of irradiation system, and it modified PANI during simple oxidative polymerization route to get polyaniline/Sm
2
O
3
-TiO
2
nanocomposite. The structural, morphology and electrochemical properties of as-synthesized polyaniline /Sm
2
O
3
-TiO
2
nanocomposite have been estimated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), Field Emission scanning electron microscope (FE-SEM), Chronopotentiometry (CP), Cyclic voltammetry (CV) and Electrochemical Impedance spectroscopy (EIS). The measurements from XRD exhibit synthesis anatase TiO
2
phase with tetragonal structure and (monoclinic and cubic) mixture structure of Sm
2
O
3
. The FE-SEM images display prepare spherical nanoparticles that covered fiber morphology of polyaniline. Interestingly the synthesized polyaniline/Sm
2
O
3
-TiO
2
nanocomposite demonstrates supercapacitance properties with value 881F/g and 141wh/kg, which observed to be larger than pure polyaniline and polyaniline/Sm
2
O
3
. In addition to, the galvanostatic charge–discharge (GCD) properties obtained the nature of pseudocapacitive for PANI/Sm
2
O
3
-TiO
2
nanocomposite. The EIS results exhibit the superior electrochemical behavior for PANI/TiO
2
-Sm
2
O
3
compared with PANI and TiO
2
-Sm
2
O
3
. |
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ISSN: | 0366-6352 1336-9075 2585-7290 |
DOI: | 10.1007/s11696-021-01948-6 |