Serveur d'exploration sur le cobalt au Maghreb

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Electrocatalytic activity and stability of La1-xCaxCoO3 perovskite-type oxides in alkaline medium

Identifieur interne : 000080 ( PascalFrancis/Curation ); précédent : 000079; suivant : 000081

Electrocatalytic activity and stability of La1-xCaxCoO3 perovskite-type oxides in alkaline medium

Auteurs : Abdelkrim Kahoul [Algérie] ; Abderrezak Hammouche [Allemagne] ; Gérard Poillerat [France] ; Rik W. De Doncker [Allemagne]

Source :

RBID : Pascal:04-0235916

Descripteurs français

English descriptors

Abstract

Electrocatalytic activity versus oxygen evolution of perovskite-type cobalt oxide (La1-xCaxCoO3, with x = 0.0, 0.2, 0.4 and 0.6) was evaluated by potentiostatic polarization technique, as a function of the electrode chemical composition. Stability of the electrode material in alkaline medium under stressing galvanostatic conditions was investigated. Highly sensitive differential pulse adsorptive stripping voltammetry (DPAdSV) technique was successfully applied for determination of traces of dissolved cobalt in the electrolyte solution. The results point out the optimum electrode activity and stability of the x = 0.4 composition.
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A08 01  1  ENG  @1 Electrocatalytic activity and stability of La1-xCaxCoO3 perovskite-type oxides in alkaline medium
A09 01  1  ENG  @1 Emerging Materials
A11 01  1    @1 KAHOUL (Abdelkrim)
A11 02  1    @1 HAMMOUCHE (Abderrezak)
A11 03  1    @1 POILLERAT (Gérard)
A11 04  1    @1 DE DONCKER (Rik W.)
A12 01  1    @1 GARIN (François) @9 ed.
A12 02  1    @1 PARLEBAS (Jean-Claude) @9 ed.
A12 03  1    @1 MINOT (Christian) @9 ed.
A12 04  1    @1 GUEMMAZ (Mohamed) @9 ed.
A14 01      @1 Laboratory for Energetics and Electrochemistry of Solids, Department of Processes Engineering E Abbas University of Setif @2 19000 Setif @3 DZA @Z 1 aut.
A14 02      @1 Institute for Power Electronics and Electrical Drives, Aachen University of Technology, Jägerstr. 17-19 @2 52066 Aachen @3 DEU @Z 2 aut. @Z 4 aut.
A14 03      @1 Laboratoire d'Electrochimie et Chimie Physique du Corps Solide, UMR CNRS/ULP 7512, 4 Rue Blaise Pascal @2 67000 Strasbourg @3 FRA @Z 3 aut.
A15 01      @1 Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515-CNRS-ECPM-ULP, 25 rue Becquerel @2 67087 Strasbourg @3 FRA @Z 1 aut.
A15 02      @1 Institut de physique et Chimie des Matériaux (IPCMS), Université Louis Pasteur, UMR 7504 du CNRS, 23 rue du Loess, BP 43 @2 67034 Strasbourg @3 FRA @Z 2 aut.
A15 03      @1 Laboratoire de Chimie Théorique, Boîte 137, UPMC @2 75252 Paris @3 FRA @Z 3 aut.
A15 04      @1 Faculté des Sciences, Université Ferhat Abbas @2 19000 Sétif @3 DZA @Z 4 aut.
A18 01  1    @1 Ferhat Abbas University of Setif @2 19000 Setif @3 DZA @9 patr.
A20       @1 287-291
A21       @1 2004
A23 01      @0 ENG
A43 01      @1 INIST @2 21357 @5 354000116771020040
A44       @0 0000 @1 © 2004 INIST-CNRS. All rights reserved.
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C01 01    ENG  @0 Electrocatalytic activity versus oxygen evolution of perovskite-type cobalt oxide (La1-xCaxCoO3, with x = 0.0, 0.2, 0.4 and 0.6) was evaluated by potentiostatic polarization technique, as a function of the electrode chemical composition. Stability of the electrode material in alkaline medium under stressing galvanostatic conditions was investigated. Highly sensitive differential pulse adsorptive stripping voltammetry (DPAdSV) technique was successfully applied for determination of traces of dissolved cobalt in the electrolyte solution. The results point out the optimum electrode activity and stability of the x = 0.4 composition.
C02 01  X    @0 001C01A03
C03 01  X  FRE  @0 Stabilité @5 01
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C03 01  X  SPA  @0 Estabilidad @5 01
C03 02  X  FRE  @0 Perovskite @5 02
C03 02  X  ENG  @0 Perovskite @5 02
C03 02  X  SPA  @0 Perovskita @5 02
C03 03  X  FRE  @0 Oxyde @2 NA @5 03
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C03 04  X  ENG  @0 Cobalt oxide @5 04
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C03 05  X  FRE  @0 Voltammétrie @5 05
C03 05  X  ENG  @0 Voltammetry @5 05
C03 05  X  SPA  @0 Voltametría @5 05
N21       @1 152
N82       @1 OTO
pR  
A30 01  1  ENG  @1 French-Algerian Scientific Congress @2 1 @3 Tamanrasset DZA @4 2003-02-22

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<sub>1-x</sub>
Ca
<sub>x</sub>
CoO
<sub>3</sub>
, with x = 0.0, 0.2, 0.4 and 0.6) was evaluated by potentiostatic polarization technique, as a function of the electrode chemical composition. Stability of the electrode material in alkaline medium under stressing galvanostatic conditions was investigated. Highly sensitive differential pulse adsorptive stripping voltammetry (DPAdSV) technique was successfully applied for determination of traces of dissolved cobalt in the electrolyte solution. The results point out the optimum electrode activity and stability of the x = 0.4 composition.</div>
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<sub>1-x</sub>
Ca
<sub>x</sub>
CoO
<sub>3</sub>
, with x = 0.0, 0.2, 0.4 and 0.6) was evaluated by potentiostatic polarization technique, as a function of the electrode chemical composition. Stability of the electrode material in alkaline medium under stressing galvanostatic conditions was investigated. Highly sensitive differential pulse adsorptive stripping voltammetry (DPAdSV) technique was successfully applied for determination of traces of dissolved cobalt in the electrolyte solution. The results point out the optimum electrode activity and stability of the x = 0.4 composition.</s0>
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