A comparative study of the anion transfer kinetics across a water/nitrobenzene interface by means of electrochemical impedance spectroscopy and square-wave voltammetry at thin organic film-modified electrodes

The kinetics of the transfer of a series of hydrophilic monovalent anions across the water/nitrobenzene (W/NB) interface has been studied by means of thin organic film-modified electrodes in combination with electrochemical impedance spectroscopy and square-wave voltammetry. The studied ions are Cl-...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1991. - 22(2006), 7 vom: 28. März, Seite 3404-12
1. Verfasser: Gulaboski, Rubin (VerfasserIn)
Weitere Verfasser: Mirćeski, Valentin, Pereira, Carlos M, Cordeiro, M Natalia D S, Silva, A Fernando, Quentel, François, L'Her, Maurice, Lovrić, Milivoj
Format: Aufsatz
Sprache:English
Veröffentlicht: 2006
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
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245 1 2 |a A comparative study of the anion transfer kinetics across a water/nitrobenzene interface by means of electrochemical impedance spectroscopy and square-wave voltammetry at thin organic film-modified electrodes 
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520 |a The kinetics of the transfer of a series of hydrophilic monovalent anions across the water/nitrobenzene (W/NB) interface has been studied by means of thin organic film-modified electrodes in combination with electrochemical impedance spectroscopy and square-wave voltammetry. The studied ions are Cl-, Br-, I-, ClO4-, NO3-, SCN-, and CH3COO-. The electrode assembly comprises a graphite electrode (GE) covered with a thin NB film containing a neutral strongly hydrophobic redox probe (decamethylferrocene or lutetium bis(tetra-tert-butylphthalocyaninato)) and an organic supporting electrolyte. The modified electrode is immersed in an aqueous solution containing a supporting electrolyte and transferring ions, and used in a conventional three-electrode configuration. Upon oxidation of the redox probe, the overall electrochemical process proceeds as an electron-ion charge-transfer reaction coupling the electron transfer at the GE/NB interface and compensates ion transfer across the W/NB interface. The rate of the ion transfer across the W/NB interface is the limiting step in the kinetics of the overall coupled electron-ion transfer reaction. Moreover, the transferring ion that is initially present in the aqueous phase only at a concentration lower than the redox probe, controls the mass transfer regime in the overall reaction. A rate equation describing the kinetics of the ion transfer that is valid for the conditions at thin organic film-modified electrodes is derived. Kinetic data measured with two electrochemical techniques are in very good agreement 
650 4 |a Journal Article 
700 1 |a Mirćeski, Valentin  |e verfasserin  |4 aut 
700 1 |a Pereira, Carlos M  |e verfasserin  |4 aut 
700 1 |a Cordeiro, M Natalia D S  |e verfasserin  |4 aut 
700 1 |a Silva, A Fernando  |e verfasserin  |4 aut 
700 1 |a Quentel, François  |e verfasserin  |4 aut 
700 1 |a L'Her, Maurice  |e verfasserin  |4 aut 
700 1 |a Lovrić, Milivoj  |e verfasserin  |4 aut 
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