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Giant Negative Thermal Expansion in the Iron Perovskite SrCu3Fe4O12
Big and cold: Strong internal compression of the Sr ion in the novel perovskite SrCu3Fe4O12 (see structure) leads to giant negative thermal expansion (NTE) between 170 and 270 K. Mössbauer spectroscopy shows charge disproportionation of FeIV to FeIII and FeV below 200 K. Thus, the isoelectric substi...
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Published in: | Angewandte Chemie (International ed.) 2011-07, Vol.50 (29), p.6579-6582 |
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creator | Yamada, Ikuya Tsuchida, Kazuki Ohgushi, Kenya Hayashi, Naoaki Kim, Jungeun Tsuji, Naruki Takahashi, Ryoji Matsushita, Masafumi Nishiyama, Norimasa Inoue, Toru Irifune, Tetsuo Kato, Kenichi Takata, Masaki Takano, Mikio |
description | Big and cold: Strong internal compression of the Sr ion in the novel perovskite SrCu3Fe4O12 (see structure) leads to giant negative thermal expansion (NTE) between 170 and 270 K. Mössbauer spectroscopy shows charge disproportionation of FeIV to FeIII and FeV below 200 K. Thus, the isoelectric substitution of the A‐site cation can induce a drastic change of the structural and electronic properties in ACu3Fe4O12 perovskites. |
doi_str_mv | 10.1002/anie.201102228 |
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Mössbauer spectroscopy shows charge disproportionation of FeIV to FeIII and FeV below 200 K. Thus, the isoelectric substitution of the A‐site cation can induce a drastic change of the structural and electronic properties in ACu3Fe4O12 perovskites.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201102228</identifier><identifier>PMID: 21648043</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>charge disproportionation ; high-pressure chemistry ; Mössbauer spectroscopy ; negative thermal expansion ; perovskite phases</subject><ispartof>Angewandte Chemie (International ed.), 2011-07, Vol.50 (29), p.6579-6582</ispartof><rights>Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2011 WILEY-VCH Verlag GmbH & Co. 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Chem. Int. Ed</addtitle><date>2011-07-11</date><risdate>2011</risdate><volume>50</volume><issue>29</issue><spage>6579</spage><epage>6582</epage><pages>6579-6582</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><notes>Ministry of Education, Culture, Sports, Science and Technology of Japan - No. 21750062</notes><notes>Priority Nanotechnology Support Program - No. 2010A1616</notes><notes>ark:/67375/WNG-H6QKQ8N6-C</notes><notes>istex:67B35C4D897A87686934FA9D61B6EB5D944E13A9</notes><notes>We thank Masahiko Isobe and Yutaka Ueda for help with the low-temperature XRD measurements at ISSP, Hiroshi Kageyama for help with the synchrotron XRD measurements, and Yuichi Shimakawa for allowing the use of the Mössbauer spectrometer. The synchrotron radiation experiments were performed at SPring-8 under the Priority Nanotechnology Support Program administered by JASRI (Proposal No. 2010A1616). This work was partly performed using the facilities of ISSP and supported by the Ministry of Education, Culture, Sports, Science and Technology of Japan with a Grant-in-Aid for Young Scientists (B) No. 21750062.</notes><notes>ArticleID:ANIE201102228</notes><notes>We thank Masahiko Isobe and Yutaka Ueda for help with the low‐temperature XRD measurements at ISSP, Hiroshi Kageyama for help with the synchrotron XRD measurements, and Yuichi Shimakawa for allowing the use of the Mössbauer spectrometer. The synchrotron radiation experiments were performed at SPring‐8 under the Priority Nanotechnology Support Program administered by JASRI (Proposal No. 2010A1616). This work was partly performed using the facilities of ISSP and supported by the Ministry of Education, Culture, Sports, Science and Technology of Japan with a Grant‐in‐Aid for Young Scientists (B) No. 21750062.</notes><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><abstract>Big and cold: Strong internal compression of the Sr ion in the novel perovskite SrCu3Fe4O12 (see structure) leads to giant negative thermal expansion (NTE) between 170 and 270 K. Mössbauer spectroscopy shows charge disproportionation of FeIV to FeIII and FeV below 200 K. Thus, the isoelectric substitution of the A‐site cation can induce a drastic change of the structural and electronic properties in ACu3Fe4O12 perovskites.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>21648043</pmid><doi>10.1002/anie.201102228</doi><tpages>4</tpages><edition>International ed. in English</edition></addata></record> |
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subjects | charge disproportionation high-pressure chemistry Mössbauer spectroscopy negative thermal expansion perovskite phases |
title | Giant Negative Thermal Expansion in the Iron Perovskite SrCu3Fe4O12 |
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