CobaltMaghrebV1, PascalFrancis, Curation, bibRecord, 000129

Zn1-xCoxO diluted magnetic semiconductors synthesized under hydrothermal conditions

Identifieur interne : 000129 ( PascalFrancis/Curation ); précédent : 000128; suivant : 000130

Zn1-xCoxO diluted magnetic semiconductors synthesized under hydrothermal conditions

Auteurs : M. Bouloudenine [France, Algérie] ; N. Viart [France] ; S. Colis [France] ; A. Dinia [France]

Source :

Catalysis today [ 0920-5861 ] ; 2006.

RBID : Pascal:06-0371434

Descripteurs français

Pascal (Inist)
- Semiconducteur, Condition hydrothermale, Métal transition composé, Film, Catalyse hétérogène, Zinc Oxyde, Cobalt Oxyde.

English descriptors

KwdEn :
- Cobalt Oxides, Film, Heterogeneous catalysis, Hydrothermal condition, Semiconductor materials, Transition element compounds, Zinc Oxides.

Abstract

Polycrystalline Zn_1-xCo_xO magnetic semiconductors were synthesized by hydrothermal technique from aqueous solutions of Zn and Co acetates using potassium hydroxide KOH as hydrolytic catalyst. The structural and magnetic properties of the samples were investigated as a function of acetates and KOH concentrations. The results show that the highest amount of Co that can be successfully inserted in the ZnO matrix is around 10%, when using concentrations of 0.5 and 0.77 mol/L of acetate and KOH, respectively. For the Zn_0.9Co_0.1O sample, X-ray diffraction indicates a pure ZnO würtzite structure free of parasitic phases in agreement with optical measurements that reveal the presence of Co²⁺ cations in substitution of Zn²⁺. The magnetization measurements show a paramagnetic behaviour and no evidence of ferromagnetism. This may be due to the absence of free carriers.

A01	`01`	`1`		`@0 0920-5861`
A02	`01`			`@0 CATTEA`
A03		`1`		`@0 Catal. today`
A05				`@2 113`
A06				`@2 3-4`
A08	`01`	`1`	`ENG`	`@1 Zn_1-xCo_xO diluted magnetic semiconductors synthesized under hydrothermal conditions`
A09	`01`	`1`	`ENG`	`@1 Catalysis, Nanomaterials and Environment`
A11	`01`	`1`		`@1 BOULOUDENINE (M.)`
A11	`02`	`1`		`@1 VIART (N.)`
A11	`03`	`1`		`@1 COLIS (S.)`
A11	`04`	`1`		`@1 DINIA (A.)`
A12	`01`	`1`		`@1 GARIN (François) @9 ed.`
A12	`02`	`1`		`@1 MAAMACHE (Mustapha) @9 ed.`
A12	`03`	`1`		`@1 SCHMERBER (Guy) @9 ed.`
A12	`04`	`1`		`@1 DEMANGEAT (Claude) @9 ed.`
A14	`01`			`@1 Institut de Physique et Chimie des Matériaux de Strasbourg, IPCMS, Groupe des Matériaux Inorganiques, CNRS-UMR 7504, ULP-ECPM, 23 Rue du Loess, BP 43 @2 67034 Strasbourg @3 FRA @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut.`
A14	`02`			`@1 Université de Annaba, Faculté des Sciences, Département de Physique, BP 12 @2 Annaba 23000 @3 DZA @Z 1 aut.`
A15	`01`			`@1 Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515-CNRS-ULP-ECPM, 25 rue Becquerel @2 67087 Strasbourg @3 FRA @Z 1 aut.`
A15	`02`			`@1 Département de Physique, Faculté des Sciences, Université Ferhat Abbas @2 1900 Sétif @3 DZA @Z 2 aut.`
A15	`03`			`@1 Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université Louis Pasteur, UMR 7504-CNRS-ULP, 23 rue du Loess, BP 43 @2 67034 Strasbourg @3 FRA @Z 3 aut. @Z 4 aut.`
A20				`@1 240-244`
A21				`@1 2006`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 21357 @5 354000142867030170`
A44				`@0 0000 @1 © 2006 INIST-CNRS. All rights reserved.`
A45				`@0 31 ref.`
A47	`01`	`1`		`@0 06-0371434`
A60				`@1 P @2 C`
A61				`@0 A`
A64	`01`	`1`		`@0 Catalysis today`
A66	`01`			`@0 NLD`
C01	`01`		`ENG`	@0 Polycrystalline Zn_1-xCo_xO magnetic semiconductors were synthesized by hydrothermal technique from aqueous solutions of Zn and Co acetates using potassium hydroxide KOH as hydrolytic catalyst. The structural and magnetic properties of the samples were investigated as a function of acetates and KOH concentrations. The results show that the highest amount of Co that can be successfully inserted in the ZnO matrix is around 10%, when using concentrations of 0.5 and 0.77 mol/L of acetate and KOH, respectively. For the Zn_0.9Co_0.1O sample, X-ray diffraction indicates a pure ZnO würtzite structure free of parasitic phases in agreement with optical measurements that reveal the presence of Co²⁺ cations in substitution of Zn²⁺. The magnetization measurements show a paramagnetic behaviour and no evidence of ferromagnetism. This may be due to the absence of free carriers.
C02	`01`	`X`		`@0 001C01A03`
C03	`01`	`X`	`FRE`	`@0 Semiconducteur @5 01`
C03	`01`	`X`	`ENG`	`@0 Semiconductor materials @5 01`
C03	`01`	`X`	`SPA`	`@0 Semiconductor(material) @5 01`
C03	`02`	`X`	`FRE`	`@0 Condition hydrothermale @5 02`
C03	`02`	`X`	`ENG`	`@0 Hydrothermal condition @5 02`
C03	`02`	`X`	`SPA`	`@0 Condición hidrotermal @5 02`
C03	`03`	`3`	`FRE`	`@0 Métal transition composé @5 03`
C03	`03`	`3`	`ENG`	`@0 Transition element compounds @5 03`
C03	`04`	`X`	`FRE`	`@0 Film @5 04`
C03	`04`	`X`	`ENG`	`@0 Film @5 04`
C03	`04`	`X`	`SPA`	`@0 Película @5 04`
C03	`05`	`X`	`FRE`	`@0 Catalyse hétérogène @5 05`
C03	`05`	`X`	`ENG`	`@0 Heterogeneous catalysis @5 05`
C03	`05`	`X`	`SPA`	`@0 Catálisis heterogénea @5 05`
C03	`06`	`X`	`FRE`	`@0 Zinc Oxyde @2 NC @2 NA @5 06`
C03	`06`	`X`	`ENG`	`@0 Zinc Oxides @2 NC @2 NA @5 06`
C03	`06`	`X`	`SPA`	`@0 Zinc Óxido @2 NC @2 NA @5 06`
C03	`07`	`X`	`FRE`	`@0 Cobalt Oxyde @2 NC @2 NA @5 07`
C03	`07`	`X`	`ENG`	`@0 Cobalt Oxides @2 NC @2 NA @5 07`
C03	`07`	`X`	`SPA`	`@0 Cobalto Óxido @2 NC @2 NA @5 07`
N21				`@1 247`

A30	`01`	`1`	`ENG`	`@1 Colloquium on Environment, Materials, Physics and Energy @3 Ouargla DZA @4 2004-12-11`

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Le document en format XML

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Co<sub>x</sub>
O diluted magnetic semiconductors synthesized under hydrothermal conditions</title>
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O diluted magnetic semiconductors synthesized under hydrothermal conditions</title>
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<s2>67034 Strasbourg</s2>
<s3>FRA</s3>
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<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Université de Annaba, Faculté des Sciences, Département de Physique, BP 12</s1>
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<author><name sortKey="Viart, N" sort="Viart, N" uniqKey="Viart N" first="N." last="Viart">N. Viart</name>
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<s2>67034 Strasbourg</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
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<s2>67034 Strasbourg</s2>
<s3>FRA</s3>
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<series><title level="j" type="main">Catalysis today</title>
<title level="j" type="abbreviated">Catal. today</title>
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<imprint><date when="2006">2006</date>
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<seriesStmt><title level="j" type="main">Catalysis today</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cobalt Oxides</term>
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<term>Semiconductor materials</term>
<term>Transition element compounds</term>
<term>Zinc Oxides</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Semiconducteur</term>
<term>Condition hydrothermale</term>
<term>Métal transition composé</term>
<term>Film</term>
<term>Catalyse hétérogène</term>
<term>Zinc Oxyde</term>
<term>Cobalt Oxyde</term>
</keywords>
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<front><div type="abstract" xml:lang="en">Polycrystalline Zn<sub>1-x</sub>
Co<sub>x</sub>
O magnetic semiconductors were synthesized by hydrothermal technique from aqueous solutions of Zn and Co acetates using potassium hydroxide KOH as hydrolytic catalyst. The structural and magnetic properties of the samples were investigated as a function of acetates and KOH concentrations. The results show that the highest amount of Co that can be successfully inserted in the ZnO matrix is around 10%, when using concentrations of 0.5 and 0.77 mol/L of acetate and KOH, respectively. For the Zn<sub>0.9</sub>
Co<sub>0.1</sub>
O sample, X-ray diffraction indicates a pure ZnO würtzite structure free of parasitic phases in agreement with optical measurements that reveal the presence of Co<sup>2+</sup>
 cations in substitution of Zn<sup>2+</sup>
. The magnetization measurements show a paramagnetic behaviour and no evidence of ferromagnetism. This may be due to the absence of free carriers.</div>
</front>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0920-5861</s0>
</fA01>
<fA02 i1="01"><s0>CATTEA</s0>
</fA02>
<fA03 i2="1"><s0>Catal. today</s0>
</fA03>
<fA05><s2>113</s2>
</fA05>
<fA06><s2>3-4</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Zn<sub>1-x</sub>
Co<sub>x</sub>
O diluted magnetic semiconductors synthesized under hydrothermal conditions</s1>
</fA08>
<fA09 i1="01" i2="1" l="ENG"><s1>Catalysis, Nanomaterials and Environment</s1>
</fA09>
<fA11 i1="01" i2="1"><s1>BOULOUDENINE (M.)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>VIART (N.)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>COLIS (S.)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>DINIA (A.)</s1>
</fA11>
<fA12 i1="01" i2="1"><s1>GARIN (François)</s1>
<s9>ed.</s9>
</fA12>
<fA12 i1="02" i2="1"><s1>MAAMACHE (Mustapha)</s1>
<s9>ed.</s9>
</fA12>
<fA12 i1="03" i2="1"><s1>SCHMERBER (Guy)</s1>
<s9>ed.</s9>
</fA12>
<fA12 i1="04" i2="1"><s1>DEMANGEAT (Claude)</s1>
<s9>ed.</s9>
</fA12>
<fA14 i1="01"><s1>Institut de Physique et Chimie des Matériaux de Strasbourg, IPCMS, Groupe des Matériaux Inorganiques, CNRS-UMR 7504, ULP-ECPM, 23 Rue du Loess, BP 43</s1>
<s2>67034 Strasbourg</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Université de Annaba, Faculté des Sciences, Département de Physique, BP 12</s1>
<s2>Annaba 23000</s2>
<s3>DZA</s3>
<sZ>1 aut.</sZ>
</fA14>
<fA15 i1="01"><s1>Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515-CNRS-ULP-ECPM, 25 rue Becquerel</s1>
<s2>67087 Strasbourg</s2>
<s3>FRA</s3>
<sZ>1 aut.</sZ>
</fA15>
<fA15 i1="02"><s1>Département de Physique, Faculté des Sciences, Université Ferhat Abbas</s1>
<s2>1900 Sétif</s2>
<s3>DZA</s3>
<sZ>2 aut.</sZ>
</fA15>
<fA15 i1="03"><s1>Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), Université Louis Pasteur, UMR 7504-CNRS-ULP, 23 rue du Loess, BP 43</s1>
<s2>67034 Strasbourg</s2>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
</fA15>
<fA20><s1>240-244</s1>
</fA20>
<fA21><s1>2006</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>21357</s2>
<s5>354000142867030170</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2006 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>31 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>06-0371434</s0>
</fA47>
<fA60><s1>P</s1>
<s2>C</s2>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Catalysis today</s0>
</fA64>
<fA66 i1="01"><s0>NLD</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>Polycrystalline Zn<sub>1-x</sub>
Co<sub>x</sub>
O magnetic semiconductors were synthesized by hydrothermal technique from aqueous solutions of Zn and Co acetates using potassium hydroxide KOH as hydrolytic catalyst. The structural and magnetic properties of the samples were investigated as a function of acetates and KOH concentrations. The results show that the highest amount of Co that can be successfully inserted in the ZnO matrix is around 10%, when using concentrations of 0.5 and 0.77 mol/L of acetate and KOH, respectively. For the Zn<sub>0.9</sub>
Co<sub>0.1</sub>
O sample, X-ray diffraction indicates a pure ZnO würtzite structure free of parasitic phases in agreement with optical measurements that reveal the presence of Co<sup>2+</sup>
 cations in substitution of Zn<sup>2+</sup>
. The magnetization measurements show a paramagnetic behaviour and no evidence of ferromagnetism. This may be due to the absence of free carriers.</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>001C01A03</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE"><s0>Semiconducteur</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG"><s0>Semiconductor materials</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Semiconductor(material)</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Condition hydrothermale</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Hydrothermal condition</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Condición hidrotermal</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="3" l="FRE"><s0>Métal transition composé</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="3" l="ENG"><s0>Transition element compounds</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Film</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Film</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Película</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Catalyse hétérogène</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Heterogeneous catalysis</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Catálisis heterogénea</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Zinc Oxyde</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Zinc Oxides</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Zinc Óxido</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Cobalt Oxyde</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Cobalt Oxides</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Cobalto Óxido</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>07</s5>
</fC03>
<fN21><s1>247</s1>
</fN21>
</pA>
<pR><fA30 i1="01" i2="1" l="ENG"><s1>Colloquium on Environment, Materials, Physics and Energy</s1>
<s3>Ouargla DZA</s3>
<s4>2004-12-11</s4>
</fA30>
</pR>
</standard>
</inist>
</record>

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Zn1-xCoxO diluted magnetic semiconductors synthesized under hydrothermal conditions

Zn1-xCoxO diluted magnetic semiconductors synthesized under hydrothermal conditions

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