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Investigation of (R1-xR'x)2(Fe,Co)17 powders by Mössbauer spectrometry

Identifieur interne : 000210 ( PascalFrancis/Curation ); précédent : 000209; suivant : 000211

Investigation of (R1-xR'x)2(Fe,Co)17 powders by Mössbauer spectrometry

Auteurs : F. Richomme [France] ; J. M. Le Breton [France] ; M. S. Ben Kraiem [Tunisie] ; A. Cheikhrouhou [Tunisie]

Source :

RBID : Pascal:10-0383238

Descripteurs français

English descriptors

Abstract

We investigated (R1-xR'x)2Fe17 and (R1-xR'x)2Fe16Co powders by 57Fe Mössbauer spectrometry at 295 K where R and R' are Y, Nd, Sm, Gd. The spectra of the (R1-xR'x)2Fe17 compounds have been fitted with seven sextets: 18f12, 18f6, 18h12, 18h6, 9d6, 9d3 and 6c. The isomer shifts of the different Fe sites are in agreement with the Wigner-Seitz cell volumes. They do not depend on the nature of the rare earth. The hyperfine fields are consistent with the evolution of the Curie temperature. To account for substitution effects due to the partial replacement of Fe by Co, the Mössbauer spectra of the (R1-xR'x)2Fe16Co samples have been fitted with four sextets corresponding to the 18f, 18h, 9d, and 6c Fe sites, by considering the site occupancy of the Co atoms in the lattice. The evolution of the hyperfine field with the rare-earth concentration is discussed and interpreted in relation with the magnetic coupling between rare-earth and Fe magnetic sublattices, in agreement with previous magnetic measurements.
pA  
A01 01  1    @0 0925-8388
A03   1    @0 J. alloys compd.
A05       @2 494
A06       @2 1-2
A08 01  1  ENG  @1 Investigation of (R1-xR'x)2(Fe,Co)17 powders by Mössbauer spectrometry
A11 01  1    @1 RICHOMME (F.)
A11 02  1    @1 LE BRETON (J. M.)
A11 03  1    @1 BEN KRAIEM (M. S.)
A11 04  1    @1 CHEIKHROUHOU (A.)
A14 01      @1 Groupe de Physique des Matériaux, UMR CNRS 6634 @2 76801 Saint-Etienne du Rouvray @3 FRA @Z 1 aut. @Z 2 aut.
A14 02      @1 Laboratoire de Physique des Matériaux, Faculté des Sciences de Sfax, B.P. 802 @2 3018 Sfax @3 TUN @Z 3 aut. @Z 4 aut.
A20       @1 5-10
A21       @1 2010
A23 01      @0 ENG
A43 01      @1 INIST @2 1151 @5 354000191703730080
A44       @0 0000 @1 © 2010 INIST-CNRS. All rights reserved.
A45       @0 25 ref.
A47 01  1    @0 10-0383238
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of alloys and compounds
A66 01      @0 GBR
C01 01    ENG  @0 We investigated (R1-xR'x)2Fe17 and (R1-xR'x)2Fe16Co powders by 57Fe Mössbauer spectrometry at 295 K where R and R' are Y, Nd, Sm, Gd. The spectra of the (R1-xR'x)2Fe17 compounds have been fitted with seven sextets: 18f12, 18f6, 18h12, 18h6, 9d6, 9d3 and 6c. The isomer shifts of the different Fe sites are in agreement with the Wigner-Seitz cell volumes. They do not depend on the nature of the rare earth. The hyperfine fields are consistent with the evolution of the Curie temperature. To account for substitution effects due to the partial replacement of Fe by Co, the Mössbauer spectra of the (R1-xR'x)2Fe16Co samples have been fitted with four sextets corresponding to the 18f, 18h, 9d, and 6c Fe sites, by considering the site occupancy of the Co atoms in the lattice. The evolution of the hyperfine field with the rare-earth concentration is discussed and interpreted in relation with the magnetic coupling between rare-earth and Fe magnetic sublattices, in agreement with previous magnetic measurements.
C02 01  3    @0 001B70F80
C03 01  3  FRE  @0 Effet Mössbauer @5 02
C03 01  3  ENG  @0 Moessbauer effect @5 02
C03 02  3  FRE  @0 Déplacement isomère @5 03
C03 02  3  ENG  @0 Isomer shift @5 03
C03 03  3  FRE  @0 Méthode Wigner Seitz @5 04
C03 03  3  ENG  @0 Wigner-Seitz method @5 04
C03 04  X  FRE  @0 Champ magnétique hyperfin @5 05
C03 04  X  ENG  @0 Hyperfine magnetic field @5 05
C03 04  X  SPA  @0 Campo magnético hiperfino @5 05
C03 05  3  FRE  @0 Point Curie @5 06
C03 05  3  ENG  @0 Curie point @5 06
C03 06  3  FRE  @0 Sous réseau @5 07
C03 06  3  ENG  @0 Sublattices @5 07
C03 07  3  FRE  @0 Décomposition raie @5 08
C03 07  3  ENG  @0 Line splitting @5 08
C03 08  3  FRE  @0 Aimantation @5 09
C03 08  3  ENG  @0 Magnetization @5 09
C03 09  3  FRE  @0 Lanthanide alliage @5 12
C03 09  3  ENG  @0 Rare earth alloys @5 12
C03 10  3  FRE  @0 Fer alliage @5 15
C03 10  3  ENG  @0 Iron alloys @5 15
C03 11  3  FRE  @0 Cobalt alliage @5 16
C03 11  3  ENG  @0 Cobalt alloys @5 16
C03 12  3  FRE  @0 Métal transition alliage @5 48
C03 12  3  ENG  @0 Transition element alloys @5 48
N21       @1 249

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powders by Mössbauer spectrometry</title>
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(Fe,Co)
<sub>17</sub>
powders by Mössbauer spectrometry</title>
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<sZ>2 aut.</sZ>
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<name sortKey="Ben Kraiem, M S" sort="Ben Kraiem, M S" uniqKey="Ben Kraiem M" first="M. S." last="Ben Kraiem">M. S. Ben Kraiem</name>
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<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
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<term>Iron alloys</term>
<term>Isomer shift</term>
<term>Line splitting</term>
<term>Magnetization</term>
<term>Moessbauer effect</term>
<term>Rare earth alloys</term>
<term>Sublattices</term>
<term>Transition element alloys</term>
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<term>Sous réseau</term>
<term>Décomposition raie</term>
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<div type="abstract" xml:lang="en">We investigated (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
Fe
<sub>17</sub>
and (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
Fe
<sub>16</sub>
Co powders by
<sup>57</sup>
Fe Mössbauer spectrometry at 295 K where R and R' are Y, Nd, Sm, Gd. The spectra of the (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
Fe
<sub>17</sub>
compounds have been fitted with seven sextets: 18f
<sub>12</sub>
, 18f
<sub>6</sub>
, 18h
<sub>12</sub>
, 18h
<sub>6</sub>
, 9d
<sub>6</sub>
, 9d
<sub>3</sub>
and 6c. The isomer shifts of the different Fe sites are in agreement with the Wigner-Seitz cell volumes. They do not depend on the nature of the rare earth. The hyperfine fields are consistent with the evolution of the Curie temperature. To account for substitution effects due to the partial replacement of Fe by Co, the Mössbauer spectra of the (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
Fe
<sub>16</sub>
Co samples have been fitted with four sextets corresponding to the 18f, 18h, 9d, and 6c Fe sites, by considering the site occupancy of the Co atoms in the lattice. The evolution of the hyperfine field with the rare-earth concentration is discussed and interpreted in relation with the magnetic coupling between rare-earth and Fe magnetic sublattices, in agreement with previous magnetic measurements.</div>
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<s1>Investigation of (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
(Fe,Co)
<sub>17</sub>
powders by Mössbauer spectrometry</s1>
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<s0>We investigated (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
Fe
<sub>17</sub>
and (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
Fe
<sub>16</sub>
Co powders by
<sup>57</sup>
Fe Mössbauer spectrometry at 295 K where R and R' are Y, Nd, Sm, Gd. The spectra of the (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
Fe
<sub>17</sub>
compounds have been fitted with seven sextets: 18f
<sub>12</sub>
, 18f
<sub>6</sub>
, 18h
<sub>12</sub>
, 18h
<sub>6</sub>
, 9d
<sub>6</sub>
, 9d
<sub>3</sub>
and 6c. The isomer shifts of the different Fe sites are in agreement with the Wigner-Seitz cell volumes. They do not depend on the nature of the rare earth. The hyperfine fields are consistent with the evolution of the Curie temperature. To account for substitution effects due to the partial replacement of Fe by Co, the Mössbauer spectra of the (R
<sub>1-x</sub>
R'
<sub>x</sub>
)
<sub>2</sub>
Fe
<sub>16</sub>
Co samples have been fitted with four sextets corresponding to the 18f, 18h, 9d, and 6c Fe sites, by considering the site occupancy of the Co atoms in the lattice. The evolution of the hyperfine field with the rare-earth concentration is discussed and interpreted in relation with the magnetic coupling between rare-earth and Fe magnetic sublattices, in agreement with previous magnetic measurements.</s0>
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<s5>02</s5>
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<s5>03</s5>
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<s5>03</s5>
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<s5>05</s5>
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<s5>05</s5>
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<s0>Sous réseau</s0>
<s5>07</s5>
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<s0>Sublattices</s0>
<s5>07</s5>
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<s0>Décomposition raie</s0>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="3" l="ENG">
<s0>Line splitting</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="3" l="FRE">
<s0>Aimantation</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="3" l="ENG">
<s0>Magnetization</s0>
<s5>09</s5>
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<fC03 i1="09" i2="3" l="FRE">
<s0>Lanthanide alliage</s0>
<s5>12</s5>
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<fC03 i1="09" i2="3" l="ENG">
<s0>Rare earth alloys</s0>
<s5>12</s5>
</fC03>
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<s0>Fer alliage</s0>
<s5>15</s5>
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<s0>Iron alloys</s0>
<s5>15</s5>
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<s5>16</s5>
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<s5>16</s5>
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<s5>48</s5>
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   |type=    RBID
   |clé=     Pascal:10-0383238
   |texte=   Investigation of (R1-xR'x)2(Fe,Co)17 powders by Mössbauer spectrometry
}}

Wicri

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