Kinetics and mechanism of the electrochemical reduction of molecular oxygen on platinum in KOH: influence of preferred crystallographic orientation

The oxygen electroreduction reaction has been studied at both preferred oriented and conventional polycrystalline platinum rotating disc electrodes in x m KOH (0.05 ⩽ x ⩽ 3.0) aqueous solutions under oxygen saturation at 25°C. At low current densities, Tafel lines with slope -0.060 V decade⁻¹ have b...

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Detalhes bibliográficos
Autores: Zinola Sánchez, Carlos Fernando, Castro Luna Berenguer, Ana María del Carmen, Triaca, Walter Enrique, Arvia, Alejandro Jorge
Formato: artículo
Estado:Versión publicada
Fecha de publicación:1994
País:Argentina
Recursos:Universidad Nacional de La Plata
Repositorio:SEDICI (UNLP)
Idioma:inglés
OAI Identifier:oai:sedici.unlp.edu.ar:10915/146265
Acesso em linha:http://sedici.unlp.edu.ar/handle/10915/146265
Access Level:acceso abierto
Palavra-chave:Química
Platinum Electrode
Oriented Surface
Rotate Disc Electrode
Prefer Crystallographic Orientation
Oxygen Electroreduction
Descrição
Resumo:The oxygen electroreduction reaction has been studied at both preferred oriented and conventional polycrystalline platinum rotating disc electrodes in x m KOH (0.05 ⩽ x ⩽ 3.0) aqueous solutions under oxygen saturation at 25°C. At low current densities, Tafel lines with slope -0.060 V decade⁻¹ have been obtained at all platinum electrodes. At high current densities, higher Tafel slopes ranging from -0.18 to -0.40 V decade⁻¹ have been observed, depending on the type of preferred oriented Pt and KOH concentration. Rotating ring-disc electrode data have shown that a higher amount of H₂O₂ is produced on one type of preferred oriented surface at all KOH concentrations. A complex reaction scheme has been used to evaluate the electrochemical rate constants of the reaction steps at three platinum electrodes.