Magnetic Properties of Zn0.8(Fe0.1,Co0.1)O Diluted Magnetic Semiconductors: Experimental and Theoretical Investigation
Identifieur interne : 000243 ( PascalFrancis/Curation ); précédent : 000242; suivant : 000244Magnetic Properties of Zn0.8(Fe0.1,Co0.1)O Diluted Magnetic Semiconductors: Experimental and Theoretical Investigation
Auteurs : O. Mounkachi [Maroc] ; M. Boujnah [Maroc] ; H. Labrim [Maroc] ; M. Hamedoun [Maroc] ; A. Benyoussef [Maroc] ; A. El Kenz [Maroc] ; M. Loulidi [Maroc] ; B. Belhourma [Maroc] ; M. Bhihi [Maroc] ; E. K. Hlil [France]Source :
- Journal of superconductivity and novel magnetism [ 1557-1939 ] ; 2012.
Descripteurs français
- Pascal (Inist)
- Densité état électron, Diffraction RX, Microscopie électronique transmission, Cristallinité, Grosseur grain, Méthode fonctionnelle densité, Codopage, Addition fer, Hystérésis magnétique, Addition cobalt, Ferromagnétisme, Hydrogénation, Séparation phase, Semiconducteur semimagnétique, Oxyde de zinc, ZnO.
English descriptors
- KwdEn :
Abstract
Structural and magnetic properties of Zn0.8(Fe0.1, Co0.1)O bulk diluted magnetic semiconductor have been investigated using X-ray diffraction (XRD) and magnetic measurements. TEM (Transmission Electron Microscopy) images confirmed the high crystallinity and grain size of Zn0.8(Fe0.1,Co0.1)O powder, the samples were characterized by energy dispersive spectroscopy (EDS) to confirm the expected stoichiometry. This sample has been synthesized by co-precipitation route. The study of magnetization hysteresis loop measurements infers that the bulk sample of Zn0.8(Fe0.1,Co0.1)O shows a well-defined hysteresis loop at Tc (200 K) temperature, which reflects its ferromagnetic behavior. Hydrogenation treatment was used for the control of phase separation. Based on first-principles spin-density functional calculations, using the Korringa-Kohn-Rostoker method (KKR) combined with the coherent potential approximation (CPA), the ferromagnetic state energy was calculated and compared with the local-moment-disordered (LMD) state energy. The mechanism of hybridization and interaction between magnetic ions in Zn0.8(Fe0.1,Co0.1)O is also investigated.
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Magnetic Properties of Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
,Co<sub>0.1</sub>
)O Diluted Magnetic Semiconductors: Experimental and Theoretical Investigation</title>
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<author><name sortKey="Hlil, E K" sort="Hlil, E K" uniqKey="Hlil E" first="E. K." last="Hlil">E. K. Hlil</name>
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<series><title level="j" type="main">Journal of superconductivity and novel magnetism</title>
<title level="j" type="abbreviated">J. supercond. nov. magn.</title>
<idno type="ISSN">1557-1939</idno>
<imprint><date when="2012">2012</date>
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</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cobalt additions</term>
<term>Codoping</term>
<term>Crystallinity</term>
<term>Density functional method</term>
<term>Electronic density of states</term>
<term>Ferromagnetism</term>
<term>Grain size</term>
<term>Hydrogenation</term>
<term>Iron additions</term>
<term>Magnetic hysteresis</term>
<term>Phase separation</term>
<term>Semimagnetic semiconductors</term>
<term>Transmission electron microscopy</term>
<term>XRD</term>
<term>Zinc oxide</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Densité état électron</term>
<term>Diffraction RX</term>
<term>Microscopie électronique transmission</term>
<term>Cristallinité</term>
<term>Grosseur grain</term>
<term>Méthode fonctionnelle densité</term>
<term>Codopage</term>
<term>Addition fer</term>
<term>Hystérésis magnétique</term>
<term>Addition cobalt</term>
<term>Ferromagnétisme</term>
<term>Hydrogénation</term>
<term>Séparation phase</term>
<term>Semiconducteur semimagnétique</term>
<term>Oxyde de zinc</term>
<term>ZnO</term>
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<front><div type="abstract" xml:lang="en">Structural and magnetic properties of Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
, Co<sub>0.1</sub>
)O bulk diluted magnetic semiconductor have been investigated using X-ray diffraction (XRD) and magnetic measurements. TEM (Transmission Electron Microscopy) images confirmed the high crystallinity and grain size of Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
,Co<sub>0.1</sub>
)O powder, the samples were characterized by energy dispersive spectroscopy (EDS) to confirm the expected stoichiometry. This sample has been synthesized by co-precipitation route. The study of magnetization hysteresis loop measurements infers that the bulk sample of Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
,Co<sub>0.1</sub>
)O shows a well-defined hysteresis loop at T<sub>c</sub>
(200 K) temperature, which reflects its ferromagnetic behavior. Hydrogenation treatment was used for the control of phase separation. Based on first-principles spin-density functional calculations, using the Korringa-Kohn-Rostoker method (KKR) combined with the coherent potential approximation (CPA), the ferromagnetic state energy was calculated and compared with the local-moment-disordered (LMD) state energy. The mechanism of hybridization and interaction between magnetic ions in Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
,Co<sub>0.1</sub>
)O is also investigated.</div>
</front>
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(Fe<sub>0.1</sub>
,Co<sub>0.1</sub>
)O Diluted Magnetic Semiconductors: Experimental and Theoretical Investigation</s1>
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<sZ>3 aut.</sZ>
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<s5>354000506621630520</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2012 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>17 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>12-0316236</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Journal of superconductivity and novel magnetism</s0>
</fA64>
<fA66 i1="01"><s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>Structural and magnetic properties of Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
, Co<sub>0.1</sub>
)O bulk diluted magnetic semiconductor have been investigated using X-ray diffraction (XRD) and magnetic measurements. TEM (Transmission Electron Microscopy) images confirmed the high crystallinity and grain size of Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
,Co<sub>0.1</sub>
)O powder, the samples were characterized by energy dispersive spectroscopy (EDS) to confirm the expected stoichiometry. This sample has been synthesized by co-precipitation route. The study of magnetization hysteresis loop measurements infers that the bulk sample of Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
,Co<sub>0.1</sub>
)O shows a well-defined hysteresis loop at T<sub>c</sub>
(200 K) temperature, which reflects its ferromagnetic behavior. Hydrogenation treatment was used for the control of phase separation. Based on first-principles spin-density functional calculations, using the Korringa-Kohn-Rostoker method (KKR) combined with the coherent potential approximation (CPA), the ferromagnetic state energy was calculated and compared with the local-moment-disordered (LMD) state energy. The mechanism of hybridization and interaction between magnetic ions in Zn<sub>0.8</sub>
(Fe<sub>0.1</sub>
,Co<sub>0.1</sub>
)O is also investigated.</s0>
</fC01>
<fC02 i1="01" i2="3"><s0>001B70E50P</s0>
</fC02>
<fC02 i1="02" i2="3"><s0>001B70E60E</s0>
</fC02>
<fC02 i1="03" i2="3"><s0>001B70A20N</s0>
</fC02>
<fC03 i1="01" i2="3" l="FRE"><s0>Densité état électron</s0>
<s5>02</s5>
</fC03>
<fC03 i1="01" i2="3" l="ENG"><s0>Electronic density of states</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="3" l="FRE"><s0>Diffraction RX</s0>
<s5>03</s5>
</fC03>
<fC03 i1="02" i2="3" l="ENG"><s0>XRD</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="3" l="FRE"><s0>Microscopie électronique transmission</s0>
<s5>04</s5>
</fC03>
<fC03 i1="03" i2="3" l="ENG"><s0>Transmission electron microscopy</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Cristallinité</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Crystallinity</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Cristalinidad</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="3" l="FRE"><s0>Grosseur grain</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="3" l="ENG"><s0>Grain size</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="3" l="FRE"><s0>Méthode fonctionnelle densité</s0>
<s5>07</s5>
</fC03>
<fC03 i1="06" i2="3" l="ENG"><s0>Density functional method</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Codopage</s0>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Codoping</s0>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Codrogado</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="3" l="FRE"><s0>Addition fer</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="3" l="ENG"><s0>Iron additions</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="3" l="FRE"><s0>Hystérésis magnétique</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="3" l="ENG"><s0>Magnetic hysteresis</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="3" l="FRE"><s0>Addition cobalt</s0>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="3" l="ENG"><s0>Cobalt additions</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="3" l="FRE"><s0>Ferromagnétisme</s0>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="3" l="ENG"><s0>Ferromagnetism</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="3" l="FRE"><s0>Hydrogénation</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="3" l="ENG"><s0>Hydrogenation</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="3" l="FRE"><s0>Séparation phase</s0>
<s5>14</s5>
</fC03>
<fC03 i1="13" i2="3" l="ENG"><s0>Phase separation</s0>
<s5>14</s5>
</fC03>
<fC03 i1="14" i2="3" l="FRE"><s0>Semiconducteur semimagnétique</s0>
<s5>15</s5>
</fC03>
<fC03 i1="14" i2="3" l="ENG"><s0>Semimagnetic semiconductors</s0>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Oxyde de zinc</s0>
<s5>16</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG"><s0>Zinc oxide</s0>
<s5>16</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA"><s0>Zinc óxido</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="3" l="FRE"><s0>ZnO</s0>
<s4>INC</s4>
<s5>52</s5>
</fC03>
<fN21><s1>240</s1>
</fN21>
</pA>
</standard>
</inist>
</record>
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