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Fe L 2,3 linear and circular magnetic dichroism of Fe3O4

Identifieur interne : 002369 ( Istex/Corpus ); précédent : 002368; suivant : 002370

Fe L 2,3 linear and circular magnetic dichroism of Fe3O4

Auteurs : P. Kuiper ; B. G Searle ; L.-C Duda ; R. M Wolf ; P. J Van Der Zaag

Source :

RBID : ISTEX:A00AB1CA9BFE93B30C4DE86A1EC45F6E46A31319

English descriptors

Abstract

Abstract: Measurements of circular and linear magnetic dichroism at the Fe 2p edges of Fe3O4 are presented. The dichroism results from the ferrimagnetic ordering of Fe d5 and d6 ions in octahedral and tetrahedral sites. Atomic calculations taking into account the different crystal fields have been fitted to all L-edge spectra of this compound. A chemical shift of 1.5 eV between the dominant L3 peak of the octahedral Fe2+ and Fe3+ ions gives the best fit of linear and circular dichroism. We investigate whether these parameters can be transferred to predict the Fe 2p dichroism in other ferrites.

Url:
DOI: 10.1016/S0368-2048(97)00053-4

Links to Exploration step

ISTEX:A00AB1CA9BFE93B30C4DE86A1EC45F6E46A31319

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<note type="content">Fig. 1: Electron yield absorption spectra of Fe3O4 for circularly and linearly polarized light for different magnetization directions.</note>
<note type="content">Fig. 2: Stick diagrams for circularly polarized light of the three different iron sites. The resulting MCD spectra are shown as lines. In the bottom traces, the sum of energy-shifted calculated spectra is compared with the experimental MCD spectrum.</note>
<note type="content">Fig. 3: Calculations for linearly polarized light compared to the experimental results. The curves giving the sum of Td and Oh d5 sites give the results expected for linear dichroism in CoFe2O4.</note>
<note type="content">Fig. 4: Calculations for circular dichroism expected in CoFe2O4 and Li0.5Fe2.5O4, using parameters obtained from Fe3O4.</note>
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<ce:textfn>Philips Research Laboratories, Prof. Holstlaan 4, 5656 AA Eindhoven, The Netherlands</ce:textfn>
</ce:affiliation>
<ce:correspondence id="CORR1">
<ce:label>*</ce:label>
<ce:text>Corresponding author.</ce:text>
</ce:correspondence>
</ce:author-group>
<ce:abstract>
<ce:section-title>Abstract</ce:section-title>
<ce:abstract-sec>
<ce:simple-para>Measurements of circular and linear magnetic dichroism at the Fe 2p edges of Fe
<ce:inf>3</ce:inf>
O
<ce:inf>4</ce:inf>
are presented. The dichroism results from the ferrimagnetic ordering of Fe d
<ce:sup>5</ce:sup>
and d
<ce:sup>6</ce:sup>
ions in octahedral and tetrahedral sites. Atomic calculations taking into account the different crystal fields have been fitted to all
<ce:italic>L</ce:italic>
-edge spectra of this compound. A chemical shift of 1.5 eV between the dominant
<ce:italic>L</ce:italic>
<ce:inf>3</ce:inf>
peak of the octahedral Fe
<ce:sup>2+</ce:sup>
and Fe
<ce:sup>3+</ce:sup>
ions gives the best fit of linear and circular dichroism. We investigate whether these parameters can be transferred to predict the Fe 2p dichroism in other ferrites.</ce:simple-para>
</ce:abstract-sec>
</ce:abstract>
<ce:keywords class="keyword">
<ce:section-title>Keywords</ce:section-title>
<ce:keyword>
<ce:text>X-ray magnetic dichroism</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Linear dichroism</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Ferrites</ce:text>
</ce:keyword>
</ce:keywords>
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<title>Fe L 2,3 linear and circular magnetic dichroism of Fe3O4</title>
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<name type="personal">
<namePart type="given">P</namePart>
<namePart type="family">Kuiper</namePart>
<affiliation>Department of Physics, Uppsala University, Box 530, S-751 21 Uppsala, Sweden</affiliation>
<affiliation>Corresponding author.</affiliation>
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<affiliation>Department of Physics and Astronomy, University of Canterbury, Private Bag 4800, Christchurch, New Zealand</affiliation>
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<name type="personal">
<namePart type="given">L.-C</namePart>
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<affiliation>Department of Physics, Uppsala University, Box 530, S-751 21 Uppsala, Sweden</affiliation>
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<name type="personal">
<namePart type="given">R.M</namePart>
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<affiliation>Philips Research Laboratories, Prof. Holstlaan 4, 5656 AA Eindhoven, The Netherlands</affiliation>
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<name type="personal">
<namePart type="given">P.J</namePart>
<namePart type="family">van der Zaag</namePart>
<affiliation>Philips Research Laboratories, Prof. Holstlaan 4, 5656 AA Eindhoven, The Netherlands</affiliation>
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<abstract lang="en">Abstract: Measurements of circular and linear magnetic dichroism at the Fe 2p edges of Fe3O4 are presented. The dichroism results from the ferrimagnetic ordering of Fe d5 and d6 ions in octahedral and tetrahedral sites. Atomic calculations taking into account the different crystal fields have been fitted to all L-edge spectra of this compound. A chemical shift of 1.5 eV between the dominant L3 peak of the octahedral Fe2+ and Fe3+ ions gives the best fit of linear and circular dichroism. We investigate whether these parameters can be transferred to predict the Fe 2p dichroism in other ferrites.</abstract>
<note type="content">Fig. 1: Electron yield absorption spectra of Fe3O4 for circularly and linearly polarized light for different magnetization directions.</note>
<note type="content">Fig. 2: Stick diagrams for circularly polarized light of the three different iron sites. The resulting MCD spectra are shown as lines. In the bottom traces, the sum of energy-shifted calculated spectra is compared with the experimental MCD spectrum.</note>
<note type="content">Fig. 3: Calculations for linearly polarized light compared to the experimental results. The curves giving the sum of Td and Oh d5 sites give the results expected for linear dichroism in CoFe2O4.</note>
<note type="content">Fig. 4: Calculations for circular dichroism expected in CoFe2O4 and Li0.5Fe2.5O4, using parameters obtained from Fe3O4.</note>
<subject>
<genre>Keywords</genre>
<topic>X-ray magnetic dichroism</topic>
<topic>Linear dichroism</topic>
<topic>Ferrites</topic>
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<identifier type="ISSN">0368-2048</identifier>
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<accessCondition type="use and reproduction" contentType="copyright">©1997 Elsevier Science B.V.</accessCondition>
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