Electrocatalytic reduction of nitrite on tetraruthenated metalloporphyrins/Nafion glassy carbon modified electrode
Creators
- 1. Facultad de Ciencias, Departamento de Quimica, Universidad de Chile, Las Palmeras 3425, Casilla 653, Nunoa, Santiago (Chile)
- 2. Facultad de Quimica y Biologia, Departamento de Quimica de los Materiales, Universidad de Santiago de Chile, Santiago (Chile)
- 3. Facultad de Ciencias Quimicas y Farmaceuticas, Departamento de Quimica Farmacologica y Toxicologica, Universidad de Chile, Santiago (Chile)
- 4. Departamento de Quimica Fisica y Analitica, Universidad de Jaume I, Castellon (Spain)
Description
Highlights: → Preparation and characterization of modified electrodes with M(II) Tetraruthenated porphyrins onto a Nafion film. → The electrodes were characterized by SEM, TEM, AFM and SECM techniques. → The modified electrodes are active in the electrochemical reduction of nitrite at -660 mV vs Ag/AgCl. → GC/Nf/CoTRP modified electrode is more electrochemically active than their Ni and Zn analogues. - Abstract: This paper describes the electrochemical reduction of nitrite ion in neutral aqueous solution mediated by tetraruthenated metalloporphyrins (Co(II), Ni(II) and Zn(II)) electrostatically assembled onto a Nafion film previously adsorbed on glassy carbon or ITO electrodes. Scanning electron microscope (SEM-EDX) and transmission electron microscopy (TEM) results have shown that on ITO electrodes the macrocycles forms multiple layers with a disordered stacking orientation over the Nafion film occupying hydrophobic and hydrophilic sites in the polyelectrolyte. Atomic force microscopy (AFM) results demonstrated that the Nafion film is 35 nm thick and tetraruthenated metalloporphyrins layers 190 nm thick presenting a thin but compacted morphology. Scanning electrochemical microscopy (SECM) images shows that the Co(II) tetraruthenated porphyrins/Nf/GC modified electrode is more electrochemically active than their Ni and Zn analogues. These modified electrodes are able to reduce nitrite at -660 mV showing enhanced reduction current and a decrease in the required overpotential compared to bare glassy carbon electrode. Controlled potential electrolysis experiments verify the production of ammonia, hydrazine and hydroxylamine at potentials where reduction of solvent is plausible demonstrating some selectivity toward the nitrite ion. Rotating disc electrode voltammetry shows that the factor that governs the kinetics of nitrite reduction is the charge propagation in the film.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2011.07.057Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2011.07.057;
- PII
- S0013-4686(11)01101-7;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 56
- Journal Issue
- 24
- Journal Page Range
- p. 8484-8491
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 43045039
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- AMMONIA; AQUEOUS SOLUTIONS; ATOMIC FORCE MICROSCOPY; CARBON; ELECTROCHEMISTRY; ELECTRODES; ELECTROLYSIS; FILMS; HYDRAZINE; HYDROXYLAMINE; LAYERS; MORPHOLOGY; NITRITES; PORPHYRINS; SCANNING ELECTRON MICROSCOPY; SILVER CHLORIDES; TRANSMISSION ELECTRON MICROSCOPY; VOLTAMETRY
- Descriptors DEC
- AMINES; CARBOXYLIC ACIDS; CHEMISTRY; CHLORIDES; CHLORINE COMPOUNDS; DISPERSIONS; ELECTRON MICROSCOPY; ELEMENTS; HALIDES; HALOGEN COMPOUNDS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; HOMOGENEOUS MIXTURES; HYDRIDES; HYDROGEN COMPOUNDS; LYSIS; MICROSCOPY; MIXTURES; NITROGEN COMPOUNDS; NITROGEN HYDRIDES; NONMETALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; OXYGEN COMPOUNDS; SILVER COMPOUNDS; SOLUTIONS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.