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Pulsed electrosynthesis of polypyrrole in N-butyl-N-methyl-pyrrolidinium bis(trifluoromethanesulfonyl)imide ionic liquid for electrochemical sensors

TitoloPulsed electrosynthesis of polypyrrole in N-butyl-N-methyl-pyrrolidinium bis(trifluoromethanesulfonyl)imide ionic liquid for electrochemical sensors
Tipo di pubblicazionePresentazione a Congresso
Anno di Pubblicazione2010
AutoriZane, D., Bianchini C., Appetecchi Giovanni Battista, Curulli A., and Passerini S.
Conference NameECS Transactions
Conference LocationVienna
ISBN Number9781566778053
Parole chiaveAqueous solutions, Biosensors, Bis(trifluoromethane sulfonyl)imide, Detection methods, Electrochemical corrosion, Electrochemical impedance spectroscopy, Electrochemical platforms, Electrodes, Functionalized, Glucose, Glucose oxidase, Glucose sensors, Highly sensitive, Hydrogen Peroxide, Ionic liquids, Platinum, Platinum electrodes, Polypyrroles, Pulse deposition, Pulse methods, Pyrrolidinium
Abstract

Polypyrrole (pPy) thin films were synthesized electrochemically by a pulse method on platinum electrodes in N-butyl-N-methyl-pyrrolidinium bis(trifluoromethanesulfonyl)imide ionic liquid (PYR 14TFSI). The pulse deposition method allowed the synthesis of well adherent pPy layers on Pt that are attractive for the realization of sensors and biosensors because of their good selectivity with respect to the most common interferants. The EIS (Electrochemical Impedance Spectroscopy) response to hydrogen peroxide and biological interferants indicated pPy as a highly sensitive electrochemical platform for the impedimetric sensing of H 2O 2. The polymer was overoxidized (opPy) before the characterization to prevent its electrochemical contribution in aqueous solution. Then opPy was functionalized by glucose oxidase enzyme and the device was assembled and tested as a impedimetric biosensor. This technique showed to have great chances to substitute classic detection methods. ©The Electrochemical Society.

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-79952767853&doi=10.1149%2f1.3324744&partnerID=40&md5=7732131d1497cc60c54d8c7d34183531
DOI10.1149/1.3324744
Citation KeyZane201063