Enhancing the Supercapacitive and Conductivity Properties of Polypyrrole via In-situ Polymerization with HY Zeolite Nanoparticles

Highly stable zeolite HY/polypyrrole composite material was successfully fabricated by applying in-situ chemical polymerization approach. The functional properties of the prepared zeolite HY particles/polypyrrole were systematically inspected using XRD and FT-IR characterization techniques. Thermal...

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Veröffentlicht in:Journal of inorganic and organometallic polymers and materials 2021-02, Vol.31 (2), p.704-715
Hauptverfasser: Hamidouche, Fahim, Ghebache, Zohra, Boudieb, Naima, Sanad, Moustafa M. S., Djelali, Nacer-Eddine
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Sprache:eng
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Zusammenfassung:Highly stable zeolite HY/polypyrrole composite material was successfully fabricated by applying in-situ chemical polymerization approach. The functional properties of the prepared zeolite HY particles/polypyrrole were systematically inspected using XRD and FT-IR characterization techniques. Thermal stability and optical properties were consistently studied using TGA and UV–Vis spectroscopy techniques. The value of band gap energy ( E g ) of the produced zeolite HY/polypyrrole nanocomposite was lower than the values of its individual components. Cyclic voltammetry studies concluded that HY/polypyrrole electrode material with mass ratio ~ 0.4 prepared at cold polymerization conditions ~ 0 °C exhibited the highest values of specific capacitance ~ 310 F g −1 and ionic conductivity ~ 1.7 S cm −1 . The fabricated zeolite HY/polypyrrole composite material at 0 °C revealed a capacitance retention ~ 93.4%, while the other composite prepared at 25 °C possessed a capacitance retention ~ 72.4% after 500 charge/discharge cycles. The electrochemical impedance spectroscopy (EIS) measurement for the optimized composite electrode materials confirmed the cyclic stability after long term cycling of about 5000 cycles as a result of higher ionic conductivity between active material and ionic species than that value before cycling.
ISSN:1574-1443
1574-1451
DOI:10.1007/s10904-020-01707-2