Serveur d'exploration sur le cobalt au Maghreb

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On the NaxNi0.6Co0.4O2 system : Physical and electrochemical studies

Identifieur interne : 001131 ( Main/Merge ); précédent : 001130; suivant : 001132

On the NaxNi0.6Co0.4O2 system : Physical and electrochemical studies

Auteurs : I. Saadoune [Maroc] ; A. Maazaz [Maroc] ; M. Menetrier [France] ; C. Delmas [France]

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RBID : Pascal:96-0185253

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Abstract

Sodium chemical deintercalation from the NaNi0.6Co0.4O2 phase was realized by using iodine as oxidizing agent. The Na0.58Ni0.6Co0.4O2 phase obtained was used as the positive electrode in sodium batteries. Several structural transformations were observed during discharge (intercalation reaction). The magnetic and electrical study of the NaxNi0.6Co0.4O2 (x = 1, 0.80, 0.58) phases shows clearly that NiIII (t26e1 in LS configuration) is preferentially oxidized to the tetravalent state compared to COIII (t26e0 in LS configuration). The sodium diffusion coefficient was also calculated in the solid solution domains. It shows that the diffusion kinetics is faster when sodium ions are situated in a prismatic environment.

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Pascal:96-0185253

Le document en format XML

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<title xml:lang="en" level="a">On the Na
<sub>x</sub>
Ni
<sub>0.6</sub>
Co
<sub>0.4</sub>
O
<sub>2</sub>
system : Physical and electrochemical studies</title>
<author>
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<s1>Université Cadi-Ayyad, Laboratoire de Chimie du Solide Minéral, Faculté des Sciences-Semlalia, B. P. S15</s1>
<s2>Marrakesh</s2>
<s3>MAR</s3>
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<title xml:lang="en" level="a">On the Na
<sub>x</sub>
Ni
<sub>0.6</sub>
Co
<sub>0.4</sub>
O
<sub>2</sub>
system : Physical and electrochemical studies</title>
<author>
<name sortKey="Saadoune, I" sort="Saadoune, I" uniqKey="Saadoune I" first="I." last="Saadoune">I. Saadoune</name>
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<inist:fA14 i1="01">
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<s3>MAR</s3>
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<s3>MAR</s3>
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<name sortKey="Menetrier, M" sort="Menetrier, M" uniqKey="Menetrier M" first="M." last="Menetrier">M. Menetrier</name>
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<inist:fA14 i1="02">
<s1>Institut de Chimie de la Matière Condensée de Bordeaux and Ecole Nationale Supérieure de Chimie et Physique de Bordeaux, Avenue Dr. A. Schweitzer</s1>
<s2>33608 Pessac</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</inist:fA14>
<country>France</country>
<placeName>
<region type="region" nuts="2">Nouvelle-Aquitaine</region>
<region type="old region" nuts="2">Aquitaine</region>
<settlement type="city">Pessac</settlement>
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<s1>Institut de Chimie de la Matière Condensée de Bordeaux and Ecole Nationale Supérieure de Chimie et Physique de Bordeaux, Avenue Dr. A. Schweitzer</s1>
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<s3>FRA</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
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<region type="region" nuts="2">Nouvelle-Aquitaine</region>
<region type="old region" nuts="2">Aquitaine</region>
<settlement type="city">Pessac</settlement>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Cobalt Oxides</term>
<term>Desinsertion</term>
<term>Diffusion coefficient</term>
<term>Electrochemical reaction</term>
<term>Electrode material</term>
<term>Electrolyte solution</term>
<term>Intercalation compound</term>
<term>Iodine</term>
<term>Kinetics</term>
<term>Lattice parameters</term>
<term>Magnetic properties</term>
<term>Nickel Oxides</term>
<term>Non aqueous solution</term>
<term>Quaternary compound</term>
<term>Secondary cell</term>
<term>Sodium Oxides</term>
<term>XRD</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Sodium Oxyde</term>
<term>Nickel Oxyde</term>
<term>Cobalt Oxyde</term>
<term>Composé quaternaire</term>
<term>Réaction électrochimique</term>
<term>Composé insertion</term>
<term>Désinsertion</term>
<term>Iode</term>
<term>Matériau électrode</term>
<term>Accumulateur électrochimique</term>
<term>Coefficient diffusion</term>
<term>Cinétique</term>
<term>Solution électrolyte</term>
<term>Solution non aqueuse</term>
<term>XRD</term>
<term>Paramètre cristallin</term>
<term>Propriété magnétique</term>
<term>NaxNi0,6Co0,4O2</term>
<term>Co Na Ni O</term>
</keywords>
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<term>Iode</term>
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<front>
<div type="abstract" xml:lang="en">Sodium chemical deintercalation from the NaNi
<sub>0.6</sub>
Co
<sub>0.4</sub>
O
<sub>2</sub>
phase was realized by using iodine as oxidizing agent. The Na
<sub>0.58</sub>
Ni
<sub>0.6</sub>
Co
<sub>0.4</sub>
O
<sub>2</sub>
phase obtained was used as the positive electrode in sodium batteries. Several structural transformations were observed during discharge (intercalation reaction). The magnetic and electrical study of the Na
<sub>x</sub>
Ni
<sub>0.6</sub>
Co
<sub>0.4</sub>
O
<sub>2</sub>
(x = 1, 0.80, 0.58) phases shows clearly that Ni
<sup>III</sup>
(t
<sub>2</sub>
<sup>6</sup>
e
<sup>1</sup>
in LS configuration) is preferentially oxidized to the tetravalent state compared to CO
<sup>III</sup>
(t
<sub>2</sub>
<sup>6</sup>
e
<sup>0</sup>
in LS configuration). The sodium diffusion coefficient was also calculated in the solid solution domains. It shows that the diffusion kinetics is faster when sodium ions are situated in a prismatic environment.</div>
</front>
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<name sortKey="Delmas, C" sort="Delmas, C" uniqKey="Delmas C" first="C." last="Delmas">C. Delmas</name>
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