Effect of the substituent of the cation of N-octylpyridinium hexafluorophosphate in the electrical and electrochemical response of carbon paste electrodes modified with these ionic liquids
Effect of the substituent of the cation of N-octylpyridinium hexafluorophosphate in the electrical and electrochemical response of carbon paste electrodes modified with these ionic liquids
Authors
Fuenzalida, Francesca
Aravena, Daniel
Garcia, Camilo
Garcia, Macarena
Arce, Roxana
Ramirez, Galo
Diaz, Carlos
Isaacs, Mauricio
del Carmen Arevalo, Maria
Aguirre, Maria J.
Aravena, Daniel
Garcia, Camilo
Garcia, Macarena
Arce, Roxana
Ramirez, Galo
Diaz, Carlos
Isaacs, Mauricio
del Carmen Arevalo, Maria
Aguirre, Maria J.
Authors
Date
Datos de publicaciĆ³n:
ELECTROCHIMICA ACTA,Vol.258,959-969,2017
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Abstract
A series of N-octylpyridinium hexafluorophosphate ionic liquids (ILs), ascribed as ROpyPF(6), where Opy = N-octylpyridinium and R are the substituents -OCH3, -CH3, -CF3 and -CN at the para position of the cation, were characterized and employed as binders in carbon paste electrodes (CILEs) to evaluate the electron donating or withdrawing effects of the substituent of the cation in physical and electrochemical properties of these CILEs. Substituents strongly affect the melting point of the ILs, the electric properties of the CILEs measured by electrochemical impedance spectroscopy, and the electrochemical behavior measured by the response for an outer-sphere reaction (ferro/ferricyanide redox couple) and for an inner-sphere irreversible reaction (oxidation of sulfite). Results show that ILs can be separated in two different groups: those that have withdrawing electron substituents and those that have donating-electron substituents. OpyPF(6) has a behavior similar to those that have withdrawing electron substituents. Carbon paste electrode prepared with mineral oil as binder (CPE) has a very different behavior and is described for comparison purposes only. Results show that the ILs with withdrawing electron substituents have more polarized cations (a more localized positive charge) acquiring a slight ionic character in comparison to the ILs with donating substituents. The electron withdrawing effect modifies the hydrogen-fluorine interactions and also the electrostatic interactions between anion and cation, modifying the electric and electrochemical response of the CILEs, resulting in more conductive and homogeneous surfaces. (C) 2017 Elsevier Ltd. All rights reserved.