Electrochemical behavior of polyaniline: A study by electrochemical impedance spectroscopy (EIS) in low-frequency

Conducting polymers are increasingly attracting the interest of many researchers in different areas due to their good conductivity, stability and easy preparation. Polyaniline is heavily studied in sensors, corrosion protection, electrochromic devices, and supercapacitors, however, even with numerou...

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Veröffentlicht in:Solid state ionics 2020-03, Vol.346, p.115198, Article 115198
Hauptverfasser: Martins, João C., de M. Neto, José C., Passos, Raimundo R., Pocrifka, Leandro A.
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Sprache:eng
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Zusammenfassung:Conducting polymers are increasingly attracting the interest of many researchers in different areas due to their good conductivity, stability and easy preparation. Polyaniline is heavily studied in sensors, corrosion protection, electrochromic devices, and supercapacitors, however, even with numerous applications, there are still few pieces of literature that report their electrochemical behavior in regions low-frequency of by electrochemical impedance spectroscopy (EIS). In this work, polyaniline was electropolymerized by galvanic synthesis (chronoamperometry) in stainless steel substrate. Its performance was evaluated by cyclic voltammetry (CV) galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS). It was observed in its low-frequency pseudocapacitive analysis, in the benzoquinone and hydroquinone intermediate regions, capacitance values above 100 mF·cm−2, and in the emeraldine state, 295 F·g−1 was obtained. Such results provide a better and detailed understanding of PANI oxidation and reduction processes and could optimize the use of the polymer in various fields of applications. •In characterization of charge-discharge, the PANIT1 the specific capacitance 295 F·g−1•Indicating that the capacitive process is controlled the Warburg diffusion•In the potential of 0.3 V that corresponds to the state of oxidation of the emeraldine base
ISSN:0167-2738
1872-7689
DOI:10.1016/j.ssi.2019.115198