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Long-term electrochemical stability of polyaniline- and polypyrrole-based hydrogels

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Abstract

Electrochemical behavior of the electroactive polymeric hydrogels based on polyaniline (PANI) and polypyrrole (PPy) was studied by applying 50,000 galvanostatic charge–discharge cycles. Influence of repetitive electrochemical charge–discharge on the structure of hydrogels was followed by SEM, WAXD and FTIR techniques. The PPy-based hydrogel was found to be more stable demonstrating capacitance retention of 73% and 45% after 5000 and 50,000 charge–discharge cycles, respectively. The decrease in electrochemical performance of PPy can be attributed mainly to overoxidation of the conducting polymer, associated with the formation of hydroxyl and carbonyl groups connected to the pyrrole rings. In the case of PANI, crosslinking of the conducting polymer during electrochemical cycling can be proposed. This leads to micro-syneresis inside the hydrogel and to the formation of porous structure at the initial stages of cycling. During long-term experiment, the crosslinking leads to the formation of a covering layer on the surface of a hydrogel and to masking of its porous structure and decreasing of degree of PANI crystallinity.

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Acknowledgements

The experimental work was facilitated by the equipment of the Research Center for X-ray Diffraction Studies at St. Petersburg State University. The authors are grateful to the Engineering Center of the St. Petersburg State Technological Institute (Technical University).

Funding

This work was funded by the Russian Foundation for Basic Research (RFBR), grant 18-03-01167 a.

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Correspondence to Michael A. Smirnov.

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The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Smirnov, M.A., Vorobiov, V.K., Kasatkin, I.A. et al. Long-term electrochemical stability of polyaniline- and polypyrrole-based hydrogels. Chem. Pap. 75, 5103–5112 (2021). https://doi.org/10.1007/s11696-021-01519-9

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  • DOI: https://doi.org/10.1007/s11696-021-01519-9

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