The dependence of composition and morphology of Formula composites on the experimental variables chosen for their anodic deposition (i.e., concentration of Formula particles in suspension, electrode potential, electrolysis charge, and angular speed of the electrode) has been investigated. The composite layers have been tested as electrode materials for oxygen evolution from basic media, and found to be rather effective electrocatalysts characterized by the following features: overpotential (?) at j = 100 mA cm-2 ca. 475 mV, Tafel slope close to 60 mV decade-1, linear dependence of j on Formula . Significant electrocatalytic activity could be achieved with a Formula loading as low as 2?10-5 g cm-2. The electrode performance was maintained during a 14 day electrolysis carried out at room temperature with j = 100 mA cm-2. Partial reduction of the composite layer was found to activate the composite electrodes, by decreasing ? to ca. 415 mV (at j = 100 mA cm-2). However this activation was not long lasting.

Electrodeposited Tl2O3-matrix composites: II. Electrocatalysis of oxygen evolution reaction on Tl2O3/Co3O4 composites

Guerriero P
1998

Abstract

The dependence of composition and morphology of Formula composites on the experimental variables chosen for their anodic deposition (i.e., concentration of Formula particles in suspension, electrode potential, electrolysis charge, and angular speed of the electrode) has been investigated. The composite layers have been tested as electrode materials for oxygen evolution from basic media, and found to be rather effective electrocatalysts characterized by the following features: overpotential (?) at j = 100 mA cm-2 ca. 475 mV, Tafel slope close to 60 mV decade-1, linear dependence of j on Formula . Significant electrocatalytic activity could be achieved with a Formula loading as low as 2?10-5 g cm-2. The electrode performance was maintained during a 14 day electrolysis carried out at room temperature with j = 100 mA cm-2. Partial reduction of the composite layer was found to activate the composite electrodes, by decreasing ? to ca. 415 mV (at j = 100 mA cm-2). However this activation was not long lasting.
1998
CHIMICA INORGANICA E DELLE SUPERFICI
Istituto di Chimica della Materia Condensata e di Tecnologie per l'Energia - ICMATE
ANODIC EVOLUTION
OXIDE
CO3O4
DEPOSITION
NICKEL
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/179339
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