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Local electronic and magnetic properties of ferro-orbital-ordered FeV2O4
Local magnetic structures of spinel-type FeV2O4 were investigated using X-ray absorption and X-ray magnetic circular dichroism (XMCD) spectroscopies for V and Fe sites and Mössbauer spectroscopy for Fe sites. XMCD spectra reveal that the Fe2+ (d6) and V3+ (d2) states are coupled antiferromagneticall...
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Published in: | Japanese Journal of Applied Physics 2018-09, Vol.57 (9) |
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container_title | Japanese Journal of Applied Physics |
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creator | Okabayashi, Jun Miyasaka, Shigeki Takahashi, Masashi Tajima, Setsuko |
description | Local magnetic structures of spinel-type FeV2O4 were investigated using X-ray absorption and X-ray magnetic circular dichroism (XMCD) spectroscopies for V and Fe sites and Mössbauer spectroscopy for Fe sites. XMCD spectra reveal that the Fe2+ (d6) and V3+ (d2) states are coupled antiferromagnetically. From the analyses of XMCD spectra using magneto-optical sum rules, we deduced that small but finite orbital magnetic moments remain in the V 3d states, which accounts for the ferro-orbital ordering in the V sites of FeV2O4 with both the complex and real orbital states coexisting accompanied by the distortion of Fe sites. X-ray absorption fine structure spectra supports the deduction that the Fe2+ and V3+ states remain unchanged during the structural phase transitions. Mössbauer spectra also suggest that the Jahn-Teller distortion in Fe sites can be a driving force in ferro-orbital ordering. |
doi_str_mv | 10.7567/JJAP.57.0902BD |
format | article |
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XMCD spectra reveal that the Fe2+ (d6) and V3+ (d2) states are coupled antiferromagnetically. From the analyses of XMCD spectra using magneto-optical sum rules, we deduced that small but finite orbital magnetic moments remain in the V 3d states, which accounts for the ferro-orbital ordering in the V sites of FeV2O4 with both the complex and real orbital states coexisting accompanied by the distortion of Fe sites. X-ray absorption fine structure spectra supports the deduction that the Fe2+ and V3+ states remain unchanged during the structural phase transitions. Mössbauer spectra also suggest that the Jahn-Teller distortion in Fe sites can be a driving force in ferro-orbital ordering.</description><identifier>ISSN: 0021-4922</identifier><identifier>EISSN: 1347-4065</identifier><identifier>DOI: 10.7567/JJAP.57.0902BD</identifier><identifier>CODEN: JJAPB6</identifier><language>eng</language><publisher>The Japan Society of Applied Physics</publisher><ispartof>Japanese Journal of Applied Physics, 2018-09, Vol.57 (9)</ispartof><rights>2018 The Japan Society of Applied Physics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.7567/JJAP.57.0902BD/pdf$$EPDF$$P50$$Giop$$H</linktopdf><link.rule.ids>314,780,784,27924,27925,38868,53840</link.rule.ids></links><search><creatorcontrib>Okabayashi, Jun</creatorcontrib><creatorcontrib>Miyasaka, Shigeki</creatorcontrib><creatorcontrib>Takahashi, Masashi</creatorcontrib><creatorcontrib>Tajima, Setsuko</creatorcontrib><title>Local electronic and magnetic properties of ferro-orbital-ordered FeV2O4</title><title>Japanese Journal of Applied Physics</title><addtitle>Jpn. J. Appl. Phys</addtitle><description>Local magnetic structures of spinel-type FeV2O4 were investigated using X-ray absorption and X-ray magnetic circular dichroism (XMCD) spectroscopies for V and Fe sites and Mössbauer spectroscopy for Fe sites. XMCD spectra reveal that the Fe2+ (d6) and V3+ (d2) states are coupled antiferromagnetically. From the analyses of XMCD spectra using magneto-optical sum rules, we deduced that small but finite orbital magnetic moments remain in the V 3d states, which accounts for the ferro-orbital ordering in the V sites of FeV2O4 with both the complex and real orbital states coexisting accompanied by the distortion of Fe sites. X-ray absorption fine structure spectra supports the deduction that the Fe2+ and V3+ states remain unchanged during the structural phase transitions. 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J. Appl. Phys</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>57</volume><issue>9</issue><issn>0021-4922</issn><eissn>1347-4065</eissn><coden>JJAPB6</coden><abstract>Local magnetic structures of spinel-type FeV2O4 were investigated using X-ray absorption and X-ray magnetic circular dichroism (XMCD) spectroscopies for V and Fe sites and Mössbauer spectroscopy for Fe sites. XMCD spectra reveal that the Fe2+ (d6) and V3+ (d2) states are coupled antiferromagnetically. From the analyses of XMCD spectra using magneto-optical sum rules, we deduced that small but finite orbital magnetic moments remain in the V 3d states, which accounts for the ferro-orbital ordering in the V sites of FeV2O4 with both the complex and real orbital states coexisting accompanied by the distortion of Fe sites. X-ray absorption fine structure spectra supports the deduction that the Fe2+ and V3+ states remain unchanged during the structural phase transitions. Mössbauer spectra also suggest that the Jahn-Teller distortion in Fe sites can be a driving force in ferro-orbital ordering.</abstract><pub>The Japan Society of Applied Physics</pub><doi>10.7567/JJAP.57.0902BD</doi><tpages>5</tpages></addata></record> |
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title | Local electronic and magnetic properties of ferro-orbital-ordered FeV2O4 |
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