CobaltMaghrebV1, PascalFrancis, Curation, bibRecord, 000067

Low temperature synthesis of LiCr0.3Co0.7O2 intercalation compounds using citrate, oxalate, succinate, and glycinate precursors

Identifieur interne : 000067 ( PascalFrancis/Curation ); précédent : 000066; suivant : 000068

Low temperature synthesis of LiCr0.3Co0.7O2 intercalation compounds using citrate, oxalate, succinate, and glycinate precursors

Auteurs : N. Amdouni [Tunisie] ; H. Zarrouk [Tunisie] ; C. Julien [France]

Source :

British ceramic transactions [ 0967-9782 ] ; 2003.

RBID : Pascal:03-0374058

Descripteurs français

Pascal (Inist)
- Etude expérimentale, Préparation chimique, Composé insertion, Basse température, Lithium oxyde, Chrome oxyde, Cobalt oxyde, Substitution ion, Procédé voie humide, Solution aqueuse, Méthode en solution, Citrate, Oxalate, Précurseur, Carboxylate, Thermogravimétrie, Analyse thermique différentielle, Diffraction RX, Microscopie électronique balayage, Spectre IR, Propriété électrochimique, Matériau électrode, LiCr0,3Co0,7O2, Co Cr Li O, Succinate, Glycinate.

English descriptors

KwdEn :
- Aqueous solution, Carboxylate, Chemical preparation, Chromium oxide, Citrate, Cobalt oxide, Differential thermal analysis, Electrochemical properties, Electrode material, Experimental study, Growth from solution, Infrared spectrum, Intercalation compound, Ion substitution, Lithium oxide, Low temperature, Oxalate, Precursor, Scanning electron microscopy, Thermogravimetry, Wet process, X ray diffraction.

Abstract

The synthesis of Cr substituted lithium cobaltate LiCr_0.3Co_0.7O₂ using four different low temperature methods is presented. These wet chemical routes involve the mixing of either acetates or nitrates of Co and Cr with a chelating agent in aqueous solution, namely citric acid for the sol-gel method, oxalic acid for the coprecipitation method, succinic acid for the pyrolysis method, or the complexing agent glycine for the combustion method. The synthesised products were characterised by TG-DTA, XRD, SEM, and FTIR. Structural analysis revealed the R 3 m space group for the solid solution. The electrochemical behaviour of LiCr_0.3Co_0.7O₂ was evaluated in a lithium cell.

A01	`01`	`1`		`@0 0967-9782`
A03		`1`		`@0 Br. ceram. trans.`
A05				`@2 102`
A06				`@2 1`
A08	`01`	`1`	`ENG`	`@1 Low temperature synthesis of LiCr_0.3Co_0.7O₂ intercalation compounds using citrate, oxalate, succinate, and glycinate precursors`
A11	`01`	`1`		`@1 AMDOUNI (N.)`
A11	`02`	`1`		`@1 ZARROUK (H.)`
A11	`03`	`1`		`@1 JULIEN (C.)`
A14	`01`			`@1 Laboratoire de Chimie des Matériaux, Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire @2 2092 El Manar II @3 TUN @Z 1 aut. @Z 2 aut.`
A14	`02`			`@1 Laboratoire des Milieux Désordonnés et Hétérogènes, CNRS-UMR 7603, Université Pierre et Marie Curie, 4 place Jussieu, case 86 @2 75252 Paris 05 @3 FRA @Z 3 aut.`
A20				`@1 27-33`
A21				`@1 2003`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 616 @5 354000118535700060`
A44				`@0 0000 @1 © 2003 INIST-CNRS. All rights reserved.`
A45				`@0 21 ref.`
A47	`01`	`1`		`@0 03-0374058`
A60				`@1 P`
A61				`@0 A`
A64	`01`	`1`		`@0 British ceramic transactions`
A66	`01`			`@0 GBR`
C01	`01`		`ENG`	@0 The synthesis of Cr substituted lithium cobaltate LiCr_0.3Co_0.7O₂ using four different low temperature methods is presented. These wet chemical routes involve the mixing of either acetates or nitrates of Co and Cr with a chelating agent in aqueous solution, namely citric acid for the sol-gel method, oxalic acid for the coprecipitation method, succinic acid for the pyrolysis method, or the complexing agent glycine for the combustion method. The synthesised products were characterised by TG-DTA, XRD, SEM, and FTIR. Structural analysis revealed the R 3 m space group for the solid solution. The electrochemical behaviour of LiCr_0.3Co_0.7O₂ was evaluated in a lithium cell.
C02	`01`	`X`		`@0 001C02B06`
C03	`01`	`X`	`FRE`	`@0 Etude expérimentale @5 01`
C03	`01`	`X`	`ENG`	`@0 Experimental study @5 01`
C03	`01`	`X`	`SPA`	`@0 Estudio experimental @5 01`
C03	`02`	`3`	`FRE`	`@0 Préparation chimique @5 02`
C03	`02`	`3`	`ENG`	`@0 Chemical preparation @5 02`
C03	`03`	`X`	`FRE`	`@0 Composé insertion @5 03`
C03	`03`	`X`	`ENG`	`@0 Intercalation compound @5 03`
C03	`03`	`X`	`SPA`	`@0 Compuesto inserción @5 03`
C03	`04`	`X`	`FRE`	`@0 Basse température @5 04`
C03	`04`	`X`	`ENG`	`@0 Low temperature @5 04`
C03	`04`	`X`	`SPA`	`@0 Baja temperatura @5 04`
C03	`05`	`X`	`FRE`	`@0 Lithium oxyde @5 05`
C03	`05`	`X`	`ENG`	`@0 Lithium oxide @5 05`
C03	`05`	`X`	`SPA`	`@0 Litio óxido @5 05`
C03	`06`	`X`	`FRE`	`@0 Chrome oxyde @5 06`
C03	`06`	`X`	`ENG`	`@0 Chromium oxide @5 06`
C03	`06`	`X`	`SPA`	`@0 Cromo óxido @5 06`
C03	`07`	`X`	`FRE`	`@0 Cobalt oxyde @5 07`
C03	`07`	`X`	`ENG`	`@0 Cobalt oxide @5 07`
C03	`07`	`X`	`SPA`	`@0 Cobalto óxido @5 07`
C03	`08`	`X`	`FRE`	`@0 Substitution ion @5 08`
C03	`08`	`X`	`ENG`	`@0 Ion substitution @5 08`
C03	`08`	`X`	`SPA`	`@0 Sustitución ión @5 08`
C03	`09`	`X`	`FRE`	`@0 Procédé voie humide @5 09`
C03	`09`	`X`	`ENG`	`@0 Wet process @5 09`
C03	`09`	`X`	`SPA`	`@0 Procedimiento vía húmeda @5 09`
C03	`10`	`X`	`FRE`	`@0 Solution aqueuse @5 10`
C03	`10`	`X`	`ENG`	`@0 Aqueous solution @5 10`
C03	`10`	`X`	`SPA`	`@0 Solución acuosa @5 10`
C03	`11`	`X`	`FRE`	`@0 Méthode en solution @5 11`
C03	`11`	`X`	`ENG`	`@0 Growth from solution @5 11`
C03	`11`	`X`	`SPA`	`@0 Método en solución @5 11`
C03	`12`	`X`	`FRE`	`@0 Citrate @1 ENT @5 12`
C03	`12`	`X`	`ENG`	`@0 Citrate @1 ENT @5 12`
C03	`12`	`X`	`SPA`	`@0 Citrato @1 ENT @5 12`
C03	`13`	`X`	`FRE`	`@0 Oxalate @1 ENT @2 NA @5 13`
C03	`13`	`X`	`ENG`	`@0 Oxalate @1 ENT @2 NA @5 13`
C03	`13`	`X`	`SPA`	`@0 Oxalato @1 ENT @2 NA @5 13`
C03	`14`	`X`	`FRE`	`@0 Précurseur @5 14`
C03	`14`	`X`	`ENG`	`@0 Precursor @5 14`
C03	`14`	`X`	`SPA`	`@0 Precursor @5 14`
C03	`15`	`X`	`FRE`	`@0 Carboxylate @5 15`
C03	`15`	`X`	`ENG`	`@0 Carboxylate @5 15`
C03	`15`	`X`	`SPA`	`@0 Carboxilato @5 15`
C03	`16`	`X`	`FRE`	`@0 Thermogravimétrie @5 16`
C03	`16`	`X`	`ENG`	`@0 Thermogravimetry @5 16`
C03	`16`	`X`	`SPA`	`@0 Termogravimetría @5 16`
C03	`17`	`X`	`FRE`	`@0 Analyse thermique différentielle @5 17`
C03	`17`	`X`	`ENG`	`@0 Differential thermal analysis @5 17`
C03	`17`	`X`	`SPA`	`@0 Análisis térmico diferencial @5 17`
C03	`18`	`X`	`FRE`	`@0 Diffraction RX @5 18`
C03	`18`	`X`	`ENG`	`@0 X ray diffraction @5 18`
C03	`18`	`X`	`SPA`	`@0 Difracción RX @5 18`
C03	`19`	`X`	`FRE`	`@0 Microscopie électronique balayage @5 19`
C03	`19`	`X`	`ENG`	`@0 Scanning electron microscopy @5 19`
C03	`19`	`X`	`SPA`	`@0 Microscopía electrónica barrido @5 19`
C03	`20`	`X`	`FRE`	`@0 Spectre IR @5 20`
C03	`20`	`X`	`ENG`	`@0 Infrared spectrum @5 20`
C03	`20`	`X`	`SPA`	`@0 Espectro IR @5 20`
C03	`21`	`X`	`FRE`	`@0 Propriété électrochimique @5 21`
C03	`21`	`X`	`ENG`	`@0 Electrochemical properties @5 21`
C03	`21`	`X`	`SPA`	`@0 Propiedad electroquímica @5 21`
C03	`22`	`X`	`FRE`	`@0 Matériau électrode @5 22`
C03	`22`	`X`	`ENG`	`@0 Electrode material @5 22`
C03	`22`	`X`	`SPA`	`@0 Material electrodo @5 22`
C03	`23`	`X`	`FRE`	`@0 LiCr0,3Co0,7O2 @1 FIN @4 INC @5 32`
C03	`24`	`X`	`FRE`	`@0 Co Cr Li O @4 INC @5 33`
C03	`25`	`X`	`FRE`	`@0 Succinate @1 ENT @4 INC @5 34`
C03	`26`	`X`	`FRE`	`@0 Glycinate @1 ENT @4 INC @5 35`
N21				`@1 265`
N82				`@1 PSI`

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Pascal:03-0374058

Le document en format XML

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Co<sub>0.7</sub>
O<sub>2</sub>
 intercalation compounds using citrate, oxalate, succinate, and glycinate precursors</title>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Low temperature synthesis of LiCr<sub>0.3</sub>
Co<sub>0.7</sub>
O<sub>2</sub>
 intercalation compounds using citrate, oxalate, succinate, and glycinate precursors</title>
<author><name sortKey="Amdouni, N" sort="Amdouni, N" uniqKey="Amdouni N" first="N." last="Amdouni">N. Amdouni</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Laboratoire de Chimie des Matériaux, Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire</s1>
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<s3>TUN</s3>
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<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Laboratoire des Milieux Désordonnés et Hétérogènes, CNRS-UMR 7603, Université Pierre et Marie Curie, 4 place Jussieu, case 86</s1>
<s2>75252 Paris 05</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">British ceramic transactions</title>
<title level="j" type="abbreviated">Br. ceram. trans.</title>
<idno type="ISSN">0967-9782</idno>
<imprint><date when="2003">2003</date>
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<seriesStmt><title level="j" type="main">British ceramic transactions</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aqueous solution</term>
<term>Carboxylate</term>
<term>Chemical preparation</term>
<term>Chromium oxide</term>
<term>Citrate</term>
<term>Cobalt oxide</term>
<term>Differential thermal analysis</term>
<term>Electrochemical properties</term>
<term>Electrode material</term>
<term>Experimental study</term>
<term>Growth from solution</term>
<term>Infrared spectrum</term>
<term>Intercalation compound</term>
<term>Ion substitution</term>
<term>Lithium oxide</term>
<term>Low temperature</term>
<term>Oxalate</term>
<term>Precursor</term>
<term>Scanning electron microscopy</term>
<term>Thermogravimetry</term>
<term>Wet process</term>
<term>X ray diffraction</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Etude expérimentale</term>
<term>Préparation chimique</term>
<term>Composé insertion</term>
<term>Basse température</term>
<term>Lithium oxyde</term>
<term>Chrome oxyde</term>
<term>Cobalt oxyde</term>
<term>Substitution ion</term>
<term>Procédé voie humide</term>
<term>Solution aqueuse</term>
<term>Méthode en solution</term>
<term>Citrate</term>
<term>Oxalate</term>
<term>Précurseur</term>
<term>Carboxylate</term>
<term>Thermogravimétrie</term>
<term>Analyse thermique différentielle</term>
<term>Diffraction RX</term>
<term>Microscopie électronique balayage</term>
<term>Spectre IR</term>
<term>Propriété électrochimique</term>
<term>Matériau électrode</term>
<term>LiCr0,3Co0,7O2</term>
<term>Co Cr Li O</term>
<term>Succinate</term>
<term>Glycinate</term>
</keywords>
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<front><div type="abstract" xml:lang="en">The synthesis of Cr substituted lithium cobaltate LiCr<sub>0.3</sub>
Co<sub>0.7</sub>
O<sub>2</sub>
 using four different low temperature methods is presented. These wet chemical routes involve the mixing of either acetates or nitrates of Co and Cr with a chelating agent in aqueous solution, namely citric acid for the sol-gel method, oxalic acid for the coprecipitation method, succinic acid for the pyrolysis method, or the complexing agent glycine for the combustion method. The synthesised products were characterised by TG-DTA, XRD, SEM, and FTIR. Structural analysis revealed the R 3 m space group for the solid solution. The electrochemical behaviour of LiCr<sub>0.3</sub>
Co<sub>0.7</sub>
O<sub>2</sub>
 was evaluated in a lithium cell.</div>
</front>
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<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0967-9782</s0>
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</fA03>
<fA05><s2>102</s2>
</fA05>
<fA06><s2>1</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Low temperature synthesis of LiCr<sub>0.3</sub>
Co<sub>0.7</sub>
O<sub>2</sub>
 intercalation compounds using citrate, oxalate, succinate, and glycinate precursors</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>AMDOUNI (N.)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>ZARROUK (H.)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>JULIEN (C.)</s1>
</fA11>
<fA14 i1="01"><s1>Laboratoire de Chimie des Matériaux, Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire</s1>
<s2>2092 El Manar II</s2>
<s3>TUN</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Laboratoire des Milieux Désordonnés et Hétérogènes, CNRS-UMR 7603, Université Pierre et Marie Curie, 4 place Jussieu, case 86</s1>
<s2>75252 Paris 05</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA20><s1>27-33</s1>
</fA20>
<fA21><s1>2003</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
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<s2>616</s2>
<s5>354000118535700060</s5>
</fA43>
<fA44><s0>0000</s0>
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</fA45>
<fA47 i1="01" i2="1"><s0>03-0374058</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>British ceramic transactions</s0>
</fA64>
<fA66 i1="01"><s0>GBR</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>The synthesis of Cr substituted lithium cobaltate LiCr<sub>0.3</sub>
Co<sub>0.7</sub>
O<sub>2</sub>
 using four different low temperature methods is presented. These wet chemical routes involve the mixing of either acetates or nitrates of Co and Cr with a chelating agent in aqueous solution, namely citric acid for the sol-gel method, oxalic acid for the coprecipitation method, succinic acid for the pyrolysis method, or the complexing agent glycine for the combustion method. The synthesised products were characterised by TG-DTA, XRD, SEM, and FTIR. Structural analysis revealed the R 3 m space group for the solid solution. The electrochemical behaviour of LiCr<sub>0.3</sub>
Co<sub>0.7</sub>
O<sub>2</sub>
 was evaluated in a lithium cell.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>001C02B06</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Etude expérimentale</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Experimental study</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Estudio experimental</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="3" l="FRE"><s0>Préparation chimique</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="3" l="ENG"><s0>Chemical preparation</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Composé insertion</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Intercalation compound</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Compuesto inserción</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Basse température</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Low temperature</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Baja temperatura</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Lithium oxyde</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Lithium oxide</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Litio óxido</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Chrome oxyde</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Chromium oxide</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Cromo óxido</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Cobalt oxyde</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Cobalt oxide</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Cobalto óxido</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Substitution ion</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Ion substitution</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Sustitución ión</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Procédé voie humide</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Wet process</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Procedimiento vía húmeda</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Solution aqueuse</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Aqueous solution</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Solución acuosa</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE"><s0>Méthode en solution</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG"><s0>Growth from solution</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA"><s0>Método en solución</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE"><s0>Citrate</s0>
<s1>ENT</s1>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG"><s0>Citrate</s0>
<s1>ENT</s1>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA"><s0>Citrato</s0>
<s1>ENT</s1>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE"><s0>Oxalate</s0>
<s1>ENT</s1>
<s2>NA</s2>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG"><s0>Oxalate</s0>
<s1>ENT</s1>
<s2>NA</s2>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA"><s0>Oxalato</s0>
<s1>ENT</s1>
<s2>NA</s2>
<s5>13</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE"><s0>Précurseur</s0>
<s5>14</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG"><s0>Precursor</s0>
<s5>14</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA"><s0>Precursor</s0>
<s5>14</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Carboxylate</s0>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG"><s0>Carboxylate</s0>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA"><s0>Carboxilato</s0>
<s5>15</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE"><s0>Thermogravimétrie</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="X" l="ENG"><s0>Thermogravimetry</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="X" l="SPA"><s0>Termogravimetría</s0>
<s5>16</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE"><s0>Analyse thermique différentielle</s0>
<s5>17</s5>
</fC03>
<fC03 i1="17" i2="X" l="ENG"><s0>Differential thermal analysis</s0>
<s5>17</s5>
</fC03>
<fC03 i1="17" i2="X" l="SPA"><s0>Análisis térmico diferencial</s0>
<s5>17</s5>
</fC03>
<fC03 i1="18" i2="X" l="FRE"><s0>Diffraction RX</s0>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="X" l="ENG"><s0>X ray diffraction</s0>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="X" l="SPA"><s0>Difracción RX</s0>
<s5>18</s5>
</fC03>
<fC03 i1="19" i2="X" l="FRE"><s0>Microscopie électronique balayage</s0>
<s5>19</s5>
</fC03>
<fC03 i1="19" i2="X" l="ENG"><s0>Scanning electron microscopy</s0>
<s5>19</s5>
</fC03>
<fC03 i1="19" i2="X" l="SPA"><s0>Microscopía electrónica barrido</s0>
<s5>19</s5>
</fC03>
<fC03 i1="20" i2="X" l="FRE"><s0>Spectre IR</s0>
<s5>20</s5>
</fC03>
<fC03 i1="20" i2="X" l="ENG"><s0>Infrared spectrum</s0>
<s5>20</s5>
</fC03>
<fC03 i1="20" i2="X" l="SPA"><s0>Espectro IR</s0>
<s5>20</s5>
</fC03>
<fC03 i1="21" i2="X" l="FRE"><s0>Propriété électrochimique</s0>
<s5>21</s5>
</fC03>
<fC03 i1="21" i2="X" l="ENG"><s0>Electrochemical properties</s0>
<s5>21</s5>
</fC03>
<fC03 i1="21" i2="X" l="SPA"><s0>Propiedad electroquímica</s0>
<s5>21</s5>
</fC03>
<fC03 i1="22" i2="X" l="FRE"><s0>Matériau électrode</s0>
<s5>22</s5>
</fC03>
<fC03 i1="22" i2="X" l="ENG"><s0>Electrode material</s0>
<s5>22</s5>
</fC03>
<fC03 i1="22" i2="X" l="SPA"><s0>Material electrodo</s0>
<s5>22</s5>
</fC03>
<fC03 i1="23" i2="X" l="FRE"><s0>LiCr0,3Co0,7O2</s0>
<s1>FIN</s1>
<s4>INC</s4>
<s5>32</s5>
</fC03>
<fC03 i1="24" i2="X" l="FRE"><s0>Co Cr Li O</s0>
<s4>INC</s4>
<s5>33</s5>
</fC03>
<fC03 i1="25" i2="X" l="FRE"><s0>Succinate</s0>
<s1>ENT</s1>
<s4>INC</s4>
<s5>34</s5>
</fC03>
<fC03 i1="26" i2="X" l="FRE"><s0>Glycinate</s0>
<s1>ENT</s1>
<s4>INC</s4>
<s5>35</s5>
</fC03>
<fN21><s1>265</s1>
</fN21>
<fN82><s1>PSI</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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	Serveur d'exploration sur le cobalt au Maghreb
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Serveur d'exploration sur le cobalt au Maghreb

Low temperature synthesis of LiCr0.3Co0.7O2 intercalation compounds using citrate, oxalate, succinate, and glycinate precursors

Low temperature synthesis of LiCr0.3Co0.7O2 intercalation compounds using citrate, oxalate, succinate, and glycinate precursors

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