Serveur d'exploration sur le cobalt au Maghreb

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Magnetic properties of Cofe1.9RE0.1O4 nanoparticles (RE = La, Ce, Nd, Sm, Eu, Gd, Tb, Ho) prepared in polyol

Identifieur interne : 000174 ( PascalFrancis/Curation ); précédent : 000173; suivant : 000175

Magnetic properties of Cofe1.9RE0.1O4 nanoparticles (RE = La, Ce, Nd, Sm, Eu, Gd, Tb, Ho) prepared in polyol

Auteurs : L. Ben Tahar [Tunisie] ; M. Artus [France] ; S. Ammar [France] ; L. S. Smiri [Tunisie] ; F. Herbst [France] ; M.-J. Vaulay [France] ; V. Richard [France] ; J.-M. Greneche [France] ; F. Villain [France] ; F. Fievet [France]

Source :

RBID : Pascal:08-0518493

Descripteurs français

English descriptors

Abstract

Highly crystalline Cofe1.9RE0.1O4 ferrite nanoparticles, where RE = La, Ce, Nd, Sm, Eu, Gd, Tb, and Ho, have been synthesized by forced hydrolysis in polyol. X-ray diffraction (XRD), transmission electron microscopy (TEM), electron energy-loss spectroscopy (EELS), 57 Fe Mossbauer spectrometry, Co K-edge X-ray absorption spectroscopy and magnetic measurements using a SQUID magnetometer were employed to investigate the effect of the substitution RE3+ ions for Fe3+ ones on the structure, the microstructure, the chemical homogeneity, and the magnetic properties of the cobalt ferrite system. All the produced particles are superparamagnetic at room temperature. Nevertheless, the substitution causes reduction of the blocking temperature which is mainly ascribed to partial cation exchange among the spinel-like sublattices of CoFe2O4 induced by the insertion of the relatively large RE3+ ions. The low-temperature saturation magnetization and coercivity appear to be greatly affected by the nature of RE3+ ions-maxima values were found for Gd3+ and Eu3+, respectively.
pA  
A01 01  1    @0 0304-8853
A02 01      @0 JMMMDC
A03   1    @0 J. magn. magn. mater.
A05       @2 320
A06       @2 23
A08 01  1  ENG  @1 Magnetic properties of Cofe1.9RE0.1O4 nanoparticles (RE = La, Ce, Nd, Sm, Eu, Gd, Tb, Ho) prepared in polyol
A11 01  1    @1 BEN TAHAR (L.)
A11 02  1    @1 ARTUS (M.)
A11 03  1    @1 AMMAR (S.)
A11 04  1    @1 SMIRI (L. S.)
A11 05  1    @1 HERBST (F.)
A11 06  1    @1 VAULAY (M.-J.)
A11 07  1    @1 RICHARD (V.)
A11 08  1    @1 GRENECHE (J.-M.)
A11 09  1    @1 VILLAIN (F.)
A11 10  1    @1 FIEVET (F.)
A14 01      @1 Unité de Recherche 99/UR12-30, Faculté des Sciences de Bizerte @2 7021 Jarzouna @3 TUN @Z 1 aut. @Z 4 aut.
A14 02      @1 ITODYS, Université Paris Diderot, UMR-CNRS 7086, 2 Place Jussieu @2 75251 Paris @3 FRA @Z 2 aut. @Z 3 aut. @Z 5 aut. @Z 6 aut. @Z 10 aut.
A14 03      @1 LMPTM, Institut Galilée, UPR-CNRS 9001, 99 Avenue Jean-Baptiste Clément @2 93430 Villetaneuse @3 FRA @Z 7 aut.
A14 04      @1 LPEC, Université du Maine, UMR-CNRS 6087, Avenue Olivier Messiaen @2 72085 Le Mans @3 FRA @Z 8 aut.
A14 05      @1 LCI2M, Université Paris 6. UMR-CNRS 7071, 4 Place Jussieu @2 75251 Paris @3 FRA @Z 9 aut.
A20       @1 3242-3250
A21       @1 2008
A23 01      @0 ENG
A43 01      @1 INIST @2 17230 @5 354000184279560070
A44       @0 0000 @1 © 2008 INIST-CNRS. All rights reserved.
A45       @0 45 ref.
A47 01  1    @0 08-0518493
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of magnetism and magnetic materials
A66 01      @0 NLD
C01 01    ENG  @0 Highly crystalline Cofe1.9RE0.1O4 ferrite nanoparticles, where RE = La, Ce, Nd, Sm, Eu, Gd, Tb, and Ho, have been synthesized by forced hydrolysis in polyol. X-ray diffraction (XRD), transmission electron microscopy (TEM), electron energy-loss spectroscopy (EELS), 57 Fe Mossbauer spectrometry, Co K-edge X-ray absorption spectroscopy and magnetic measurements using a SQUID magnetometer were employed to investigate the effect of the substitution RE3+ ions for Fe3+ ones on the structure, the microstructure, the chemical homogeneity, and the magnetic properties of the cobalt ferrite system. All the produced particles are superparamagnetic at room temperature. Nevertheless, the substitution causes reduction of the blocking temperature which is mainly ascribed to partial cation exchange among the spinel-like sublattices of CoFe2O4 induced by the insertion of the relatively large RE3+ ions. The low-temperature saturation magnetization and coercivity appear to be greatly affected by the nature of RE3+ ions-maxima values were found for Gd3+ and Eu3+, respectively.
C02 01  3    @0 001B70E75
C03 01  3  FRE  @0 Propriété magnétique @5 02
C03 01  3  ENG  @0 Magnetic properties @5 02
C03 02  3  FRE  @0 Composition chimique @5 03
C03 02  3  ENG  @0 Chemical composition @5 03
C03 03  3  FRE  @0 Diffraction RX @5 04
C03 03  3  ENG  @0 XRD @5 04
C03 04  3  FRE  @0 Microscopie électronique transmission @5 05
C03 04  3  ENG  @0 Transmission electron microscopy @5 05
C03 05  3  FRE  @0 Spectre perte énergie électron @5 06
C03 05  3  ENG  @0 Electron energy loss spectra @5 06
C03 06  3  FRE  @0 Effet Mössbauer @5 07
C03 06  3  ENG  @0 Moessbauer effect @5 07
C03 07  3  FRE  @0 Spectre absorption RX @5 08
C03 07  3  ENG  @0 X-ray absorption spectra @5 08
C03 08  X  FRE  @0 Substitution ion @5 09
C03 08  X  ENG  @0 Ion substitution @5 09
C03 08  X  SPA  @0 Sustitución ión @5 09
C03 09  3  FRE  @0 Microstructure @5 10
C03 09  3  ENG  @0 Microstructure @5 10
C03 10  X  FRE  @0 Fer Cobalt Lanthanide Oxyde Mixte @2 NC @2 NA @5 11
C03 10  X  ENG  @0 Iron Cobalt Rare earths Oxides Mixed @2 NC @2 NA @5 11
C03 10  X  SPA  @0 Mixto @2 NC @2 NA @5 11
C03 11  3  FRE  @0 Nanoparticule @5 15
C03 11  3  ENG  @0 Nanoparticles @5 15
C03 12  3  FRE  @0 Ferrites @5 16
C03 12  3  ENG  @0 Ferrites @5 16
C03 13  3  FRE  @0 Particule magnétique @5 20
C03 13  3  ENG  @0 Magnetic particles @5 20
N21       @1 343

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Pascal:08-0518493

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<title xml:lang="en" level="a">Magnetic properties of Cofe
<sub>1.9</sub>
RE
<sub>0.1</sub>
O
<sub>4</sub>
nanoparticles (RE = La, Ce, Nd, Sm, Eu, Gd, Tb, Ho) prepared in polyol</title>
<author>
<name sortKey="Ben Tahar, L" sort="Ben Tahar, L" uniqKey="Ben Tahar L" first="L." last="Ben Tahar">L. Ben Tahar</name>
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<name sortKey="Smiri, L S" sort="Smiri, L S" uniqKey="Smiri L" first="L. S." last="Smiri">L. S. Smiri</name>
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<series>
<title level="j" type="main">Journal of magnetism and magnetic materials</title>
<title level="j" type="abbreviated">J. magn. magn. mater.</title>
<idno type="ISSN">0304-8853</idno>
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<title level="j" type="main">Journal of magnetism and magnetic materials</title>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Chemical composition</term>
<term>Electron energy loss spectra</term>
<term>Ferrites</term>
<term>Ion substitution</term>
<term>Iron Cobalt Rare earths Oxides Mixed</term>
<term>Magnetic particles</term>
<term>Magnetic properties</term>
<term>Microstructure</term>
<term>Moessbauer effect</term>
<term>Nanoparticles</term>
<term>Transmission electron microscopy</term>
<term>X-ray absorption spectra</term>
<term>XRD</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Propriété magnétique</term>
<term>Composition chimique</term>
<term>Diffraction RX</term>
<term>Microscopie électronique transmission</term>
<term>Spectre perte énergie électron</term>
<term>Effet Mössbauer</term>
<term>Spectre absorption RX</term>
<term>Substitution ion</term>
<term>Microstructure</term>
<term>Fer Cobalt Lanthanide Oxyde Mixte</term>
<term>Nanoparticule</term>
<term>Ferrites</term>
<term>Particule magnétique</term>
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<front>
<div type="abstract" xml:lang="en">Highly crystalline Cofe
<sub>1.9</sub>
RE
<sub>0.1</sub>
O
<sub>4</sub>
ferrite nanoparticles, where RE = La, Ce, Nd, Sm, Eu, Gd, Tb, and Ho, have been synthesized by forced hydrolysis in polyol. X-ray diffraction (XRD), transmission electron microscopy (TEM), electron energy-loss spectroscopy (EELS),
<sup>57</sup>
Fe Mossbauer spectrometry, Co K-edge X-ray absorption spectroscopy and magnetic measurements using a SQUID magnetometer were employed to investigate the effect of the substitution RE
<sup>3+</sup>
ions for Fe
<sup>3+</sup>
ones on the structure, the microstructure, the chemical homogeneity, and the magnetic properties of the cobalt ferrite system. All the produced particles are superparamagnetic at room temperature. Nevertheless, the substitution causes reduction of the blocking temperature which is mainly ascribed to partial cation exchange among the spinel-like sublattices of CoFe
<sub>2</sub>
O
<sub>4</sub>
induced by the insertion of the relatively large RE
<sup>3+</sup>
ions. The low-temperature saturation magnetization and coercivity appear to be greatly affected by the nature of RE
<sup>3+</sup>
ions-maxima values were found for Gd
<sup>3+</sup>
and Eu
<sup>3+</sup>
, respectively.</div>
</front>
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<s1>Magnetic properties of Cofe
<sub>1.9</sub>
RE
<sub>0.1</sub>
O
<sub>4</sub>
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<fA11 i1="02" i2="1">
<s1>ARTUS (M.)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>AMMAR (S.)</s1>
</fA11>
<fA11 i1="04" i2="1">
<s1>SMIRI (L. S.)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>HERBST (F.)</s1>
</fA11>
<fA11 i1="06" i2="1">
<s1>VAULAY (M.-J.)</s1>
</fA11>
<fA11 i1="07" i2="1">
<s1>RICHARD (V.)</s1>
</fA11>
<fA11 i1="08" i2="1">
<s1>GRENECHE (J.-M.)</s1>
</fA11>
<fA11 i1="09" i2="1">
<s1>VILLAIN (F.)</s1>
</fA11>
<fA11 i1="10" i2="1">
<s1>FIEVET (F.)</s1>
</fA11>
<fA14 i1="01">
<s1>Unité de Recherche 99/UR12-30, Faculté des Sciences de Bizerte</s1>
<s2>7021 Jarzouna</s2>
<s3>TUN</s3>
<sZ>1 aut.</sZ>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>ITODYS, Université Paris Diderot, UMR-CNRS 7086, 2 Place Jussieu</s1>
<s2>75251 Paris</s2>
<s3>FRA</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>10 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>LMPTM, Institut Galilée, UPR-CNRS 9001, 99 Avenue Jean-Baptiste Clément</s1>
<s2>93430 Villetaneuse</s2>
<s3>FRA</s3>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>LPEC, Université du Maine, UMR-CNRS 6087, Avenue Olivier Messiaen</s1>
<s2>72085 Le Mans</s2>
<s3>FRA</s3>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="05">
<s1>LCI2M, Université Paris 6. UMR-CNRS 7071, 4 Place Jussieu</s1>
<s2>75251 Paris</s2>
<s3>FRA</s3>
<sZ>9 aut.</sZ>
</fA14>
<fA20>
<s1>3242-3250</s1>
</fA20>
<fA21>
<s1>2008</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>17230</s2>
<s5>354000184279560070</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2008 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>45 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>08-0518493</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Journal of magnetism and magnetic materials</s0>
</fA64>
<fA66 i1="01">
<s0>NLD</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>Highly crystalline Cofe
<sub>1.9</sub>
RE
<sub>0.1</sub>
O
<sub>4</sub>
ferrite nanoparticles, where RE = La, Ce, Nd, Sm, Eu, Gd, Tb, and Ho, have been synthesized by forced hydrolysis in polyol. X-ray diffraction (XRD), transmission electron microscopy (TEM), electron energy-loss spectroscopy (EELS),
<sup>57</sup>
Fe Mossbauer spectrometry, Co K-edge X-ray absorption spectroscopy and magnetic measurements using a SQUID magnetometer were employed to investigate the effect of the substitution RE
<sup>3+</sup>
ions for Fe
<sup>3+</sup>
ones on the structure, the microstructure, the chemical homogeneity, and the magnetic properties of the cobalt ferrite system. All the produced particles are superparamagnetic at room temperature. Nevertheless, the substitution causes reduction of the blocking temperature which is mainly ascribed to partial cation exchange among the spinel-like sublattices of CoFe
<sub>2</sub>
O
<sub>4</sub>
induced by the insertion of the relatively large RE
<sup>3+</sup>
ions. The low-temperature saturation magnetization and coercivity appear to be greatly affected by the nature of RE
<sup>3+</sup>
ions-maxima values were found for Gd
<sup>3+</sup>
and Eu
<sup>3+</sup>
, respectively.</s0>
</fC01>
<fC02 i1="01" i2="3">
<s0>001B70E75</s0>
</fC02>
<fC03 i1="01" i2="3" l="FRE">
<s0>Propriété magnétique</s0>
<s5>02</s5>
</fC03>
<fC03 i1="01" i2="3" l="ENG">
<s0>Magnetic properties</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="3" l="FRE">
<s0>Composition chimique</s0>
<s5>03</s5>
</fC03>
<fC03 i1="02" i2="3" l="ENG">
<s0>Chemical composition</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="3" l="FRE">
<s0>Diffraction RX</s0>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="3" l="ENG">
<s0>XRD</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="3" l="FRE">
<s0>Microscopie électronique transmission</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="3" l="ENG">
<s0>Transmission electron microscopy</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="3" l="FRE">
<s0>Spectre perte énergie électron</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="3" l="ENG">
<s0>Electron energy loss spectra</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="3" l="FRE">
<s0>Effet Mössbauer</s0>
<s5>07</s5>
</fC03>
<fC03 i1="06" i2="3" l="ENG">
<s0>Moessbauer effect</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="3" l="FRE">
<s0>Spectre absorption RX</s0>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="3" l="ENG">
<s0>X-ray absorption spectra</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Substitution ion</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Ion substitution</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Sustitución ión</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="3" l="FRE">
<s0>Microstructure</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="3" l="ENG">
<s0>Microstructure</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Fer Cobalt Lanthanide Oxyde Mixte</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Iron Cobalt Rare earths Oxides Mixed</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Mixto</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="3" l="FRE">
<s0>Nanoparticule</s0>
<s5>15</s5>
</fC03>
<fC03 i1="11" i2="3" l="ENG">
<s0>Nanoparticles</s0>
<s5>15</s5>
</fC03>
<fC03 i1="12" i2="3" l="FRE">
<s0>Ferrites</s0>
<s5>16</s5>
</fC03>
<fC03 i1="12" i2="3" l="ENG">
<s0>Ferrites</s0>
<s5>16</s5>
</fC03>
<fC03 i1="13" i2="3" l="FRE">
<s0>Particule magnétique</s0>
<s5>20</s5>
</fC03>
<fC03 i1="13" i2="3" l="ENG">
<s0>Magnetic particles</s0>
<s5>20</s5>
</fC03>
<fN21>
<s1>343</s1>
</fN21>
</pA>
</standard>
</inist>
</record>

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   |texte=   Magnetic properties of Cofe1.9RE0.1O4 nanoparticles (RE = La, Ce, Nd, Sm, Eu, Gd, Tb, Ho) prepared in polyol
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