Structure and properties of α-NaFeO{sub 2}-type ternary sodium iridates

The synthesis, structure, and elementary magnetic and electronic properties are reported for layered compounds of the type Na{sub 3−x}MIr{sub 2}O{sub 6} and Na{sub 3−x}M{sub 2}IrO{sub 6}, where M is a transition metal from the 3d series (M=Zn, Cu, Ni, Co, Fe and Mn). The rhombohedral structures, in...

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Veröffentlicht in:Journal of solid state chemistry 2014-02, Vol.210 (1)
Hauptverfasser: Baroudi, Kristen, Yim, Cindi, Wu, Hui, Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115, Huang, Qingzhen, Roudebush, John H., Vavilova, Eugenia, Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan, Grafe, Hans-Joachim, Kataev, Vladislav, Buechner, Bernd, Institut für Festkörperphysik, Technische Universität Dresden, Dresden, Ji, Huiwen, Kuo, Changyang, Hu, Zhiwei, Pi, Tun-Wen, Pao, Chiwen, Lee, Jyhfu, Mikhailova, Daria, Hao Tjeng, Liu, Cava, R.J.
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container_title Journal of solid state chemistry
container_volume 210
creator Baroudi, Kristen
Yim, Cindi
Wu, Hui
Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115
Huang, Qingzhen
Roudebush, John H.
Vavilova, Eugenia
Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan
Grafe, Hans-Joachim
Kataev, Vladislav
Buechner, Bernd
Institut für Festkörperphysik, Technische Universität Dresden, Dresden
Ji, Huiwen
Kuo, Changyang
Hu, Zhiwei
Pi, Tun-Wen
Pao, Chiwen
Lee, Jyhfu
Mikhailova, Daria
Hao Tjeng, Liu
Cava, R.J.
description The synthesis, structure, and elementary magnetic and electronic properties are reported for layered compounds of the type Na{sub 3−x}MIr{sub 2}O{sub 6} and Na{sub 3−x}M{sub 2}IrO{sub 6}, where M is a transition metal from the 3d series (M=Zn, Cu, Ni, Co, Fe and Mn). The rhombohedral structures, in space group R−3m, were determined by refinement of neutron and synchrotron powder diffraction data. No clear evidence for long range 2:1 or 1:2 honeycomb-like M/Ir ordering was found in the neutron powder diffraction patterns except in the case of M=Zn, and thus in general the compounds are best designated as sodium deficient α-NaFeO{sub 2}-type phases with formulas Na{sub 1−x}M{sub 1/3}Ir{sub 2/3}O{sub 2} or Na{sub 1−x}M{sub 2/3}Ir{sub 1/3}O{sub 2}. Synchrotron powder diffraction patterns indicate that several of the compounds likely have honeycomb in-plane metal–iridium ordering with disordered stacking of the layers. All the compounds are sodium deficient under our synthetic conditions and are black and insulating. Weiss constants derived from magnetic susceptibility measurements indicate that Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2}, and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} display dominant antiferromagnetic interactions. For Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2} the dominant magnetic interactions at low temperature are ferromagnetic while at high temperatures they are antiferromagnetic; there is also a change in the effective moment. Low temperature specific heat measurements (to 2 K) on Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2} indicate the presence of a broad magnetic ordering transition. X-ray absorption spectroscopy shows that iridium is at or close to the 4+ oxidation state in all compounds. {sup 23}Na nuclear magnetic resonance measurements comparing Na{sub 2}IrO{sub 3} to Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} provide strong indications that the electron spins are short-range ordered in the latter two materials. Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}, Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} are spin glasses. (CSD-numbers: Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}: 426
doi_str_mv 10.1016/J.JSSC.2013.11.017
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fullrecord <record><control><sourceid>osti</sourceid><recordid>TN_cdi_osti_scitechconnect_22274215</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>22274215</sourcerecordid><originalsourceid>FETCH-osti_scitechconnect_222742153</originalsourceid><addsrcrecordid>eNqNyjtOAzEQAFALgcTyuQCVJWqbmcl-SB0RRSlCsRR0kfFOhBGsV57ZIkIciotwJhoOQPWaZ8wNgkfA9m7rt32_8gS48IgesDsxFcKycR21z6emAiBydbNsz82FyBsAYnNfV2bTa5mjzoVtGAc7lTxx0cRi88H-fLtdWPPjp8wvlr6cHie2ymUM5WglD2n-sKmkISjLlTk7hHfh6z8vze364Wm1cVk07SUm5fga8zhy1D0RdTVhs_jf-gWViEQ4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Structure and properties of α-NaFeO{sub 2}-type ternary sodium iridates</title><source>Elsevier ScienceDirect Journals</source><creator>Baroudi, Kristen ; Yim, Cindi ; Wu, Hui ; Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115 ; Huang, Qingzhen ; Roudebush, John H. ; Vavilova, Eugenia ; Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan ; Grafe, Hans-Joachim ; Kataev, Vladislav ; Buechner, Bernd ; Institut für Festkörperphysik, Technische Universität Dresden, Dresden ; Ji, Huiwen ; Kuo, Changyang ; Hu, Zhiwei ; Pi, Tun-Wen ; Pao, Chiwen ; Lee, Jyhfu ; Mikhailova, Daria ; Hao Tjeng, Liu ; Cava, R.J.</creator><creatorcontrib>Baroudi, Kristen ; Yim, Cindi ; Wu, Hui ; Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115 ; Huang, Qingzhen ; Roudebush, John H. ; Vavilova, Eugenia ; Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan ; Grafe, Hans-Joachim ; Kataev, Vladislav ; Buechner, Bernd ; Institut für Festkörperphysik, Technische Universität Dresden, Dresden ; Ji, Huiwen ; Kuo, Changyang ; Hu, Zhiwei ; Pi, Tun-Wen ; Pao, Chiwen ; Lee, Jyhfu ; Mikhailova, Daria ; Hao Tjeng, Liu ; Cava, R.J.</creatorcontrib><description>The synthesis, structure, and elementary magnetic and electronic properties are reported for layered compounds of the type Na{sub 3−x}MIr{sub 2}O{sub 6} and Na{sub 3−x}M{sub 2}IrO{sub 6}, where M is a transition metal from the 3d series (M=Zn, Cu, Ni, Co, Fe and Mn). The rhombohedral structures, in space group R−3m, were determined by refinement of neutron and synchrotron powder diffraction data. No clear evidence for long range 2:1 or 1:2 honeycomb-like M/Ir ordering was found in the neutron powder diffraction patterns except in the case of M=Zn, and thus in general the compounds are best designated as sodium deficient α-NaFeO{sub 2}-type phases with formulas Na{sub 1−x}M{sub 1/3}Ir{sub 2/3}O{sub 2} or Na{sub 1−x}M{sub 2/3}Ir{sub 1/3}O{sub 2}. Synchrotron powder diffraction patterns indicate that several of the compounds likely have honeycomb in-plane metal–iridium ordering with disordered stacking of the layers. All the compounds are sodium deficient under our synthetic conditions and are black and insulating. Weiss constants derived from magnetic susceptibility measurements indicate that Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2}, and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} display dominant antiferromagnetic interactions. For Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2} the dominant magnetic interactions at low temperature are ferromagnetic while at high temperatures they are antiferromagnetic; there is also a change in the effective moment. Low temperature specific heat measurements (to 2 K) on Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2} indicate the presence of a broad magnetic ordering transition. X-ray absorption spectroscopy shows that iridium is at or close to the 4+ oxidation state in all compounds. {sup 23}Na nuclear magnetic resonance measurements comparing Na{sub 2}IrO{sub 3} to Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} provide strong indications that the electron spins are short-range ordered in the latter two materials. Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}, Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} are spin glasses. (CSD-numbers: Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}: 426657, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}: 426659, Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2}: 426658, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}: 426656, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2}: 426655, and Na{sub 2.8}ZnIr{sub 2}O{sub 6}: 426660.) - Graphical abstract: Diffraction patterns of Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2}: neutron diffraction patterns in the main panel and synchrotron diffraction in the insets. The patterns show a small amount of ordering in the transition metal iridium layer. Display Omitted - Highlights: • We report six ternary sodium iridates with the α-NaFeO{sub 2} structure. • Compounds Na{sub 1−x}M{sub 1/3}Ir{sub 2/3}O{sub 2}, M=Co, Ni, Cu, Zn and Na{sub 1−x}M{sub 2/3}Ir{sub 1/3}O{sub 2}, M=Mn, Fe. • Rietveld refinement of powder neutron diffraction data. • All compounds are spin glasses. • NMR comparison to Na{sub 2}IrO{sub 3}.</description><identifier>ISSN: 0022-4596</identifier><identifier>EISSN: 1095-726X</identifier><identifier>DOI: 10.1016/J.JSSC.2013.11.017</identifier><language>eng</language><publisher>United States</publisher><subject>ABSORPTION SPECTROSCOPY ; ANTIFERROMAGNETISM ; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY ; INTERACTIONS ; IRIDIUM ; MAGNETIC SUSCEPTIBILITY ; MAGNETIZATION ; NEUTRON DIFFRACTION ; NEUTRONS ; NUCLEAR MAGNETIC RESONANCE ; POWDERS ; SODIUM ; SPACE GROUPS ; SPECIFIC HEAT ; SPIN GLASS STATE ; SYNCHROTRONS ; SYNTHESIS ; TRIGONAL LATTICES ; X-RAY SPECTROSCOPY</subject><ispartof>Journal of solid state chemistry, 2014-02, Vol.210 (1)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/22274215$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Baroudi, Kristen</creatorcontrib><creatorcontrib>Yim, Cindi</creatorcontrib><creatorcontrib>Wu, Hui</creatorcontrib><creatorcontrib>Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115</creatorcontrib><creatorcontrib>Huang, Qingzhen</creatorcontrib><creatorcontrib>Roudebush, John H.</creatorcontrib><creatorcontrib>Vavilova, Eugenia</creatorcontrib><creatorcontrib>Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan</creatorcontrib><creatorcontrib>Grafe, Hans-Joachim</creatorcontrib><creatorcontrib>Kataev, Vladislav</creatorcontrib><creatorcontrib>Buechner, Bernd</creatorcontrib><creatorcontrib>Institut für Festkörperphysik, Technische Universität Dresden, Dresden</creatorcontrib><creatorcontrib>Ji, Huiwen</creatorcontrib><creatorcontrib>Kuo, Changyang</creatorcontrib><creatorcontrib>Hu, Zhiwei</creatorcontrib><creatorcontrib>Pi, Tun-Wen</creatorcontrib><creatorcontrib>Pao, Chiwen</creatorcontrib><creatorcontrib>Lee, Jyhfu</creatorcontrib><creatorcontrib>Mikhailova, Daria</creatorcontrib><creatorcontrib>Hao Tjeng, Liu</creatorcontrib><creatorcontrib>Cava, R.J.</creatorcontrib><title>Structure and properties of α-NaFeO{sub 2}-type ternary sodium iridates</title><title>Journal of solid state chemistry</title><description>The synthesis, structure, and elementary magnetic and electronic properties are reported for layered compounds of the type Na{sub 3−x}MIr{sub 2}O{sub 6} and Na{sub 3−x}M{sub 2}IrO{sub 6}, where M is a transition metal from the 3d series (M=Zn, Cu, Ni, Co, Fe and Mn). The rhombohedral structures, in space group R−3m, were determined by refinement of neutron and synchrotron powder diffraction data. No clear evidence for long range 2:1 or 1:2 honeycomb-like M/Ir ordering was found in the neutron powder diffraction patterns except in the case of M=Zn, and thus in general the compounds are best designated as sodium deficient α-NaFeO{sub 2}-type phases with formulas Na{sub 1−x}M{sub 1/3}Ir{sub 2/3}O{sub 2} or Na{sub 1−x}M{sub 2/3}Ir{sub 1/3}O{sub 2}. Synchrotron powder diffraction patterns indicate that several of the compounds likely have honeycomb in-plane metal–iridium ordering with disordered stacking of the layers. All the compounds are sodium deficient under our synthetic conditions and are black and insulating. Weiss constants derived from magnetic susceptibility measurements indicate that Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2}, and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} display dominant antiferromagnetic interactions. For Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2} the dominant magnetic interactions at low temperature are ferromagnetic while at high temperatures they are antiferromagnetic; there is also a change in the effective moment. Low temperature specific heat measurements (to 2 K) on Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2} indicate the presence of a broad magnetic ordering transition. X-ray absorption spectroscopy shows that iridium is at or close to the 4+ oxidation state in all compounds. {sup 23}Na nuclear magnetic resonance measurements comparing Na{sub 2}IrO{sub 3} to Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} provide strong indications that the electron spins are short-range ordered in the latter two materials. Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}, Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} are spin glasses. (CSD-numbers: Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}: 426657, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}: 426659, Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2}: 426658, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}: 426656, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2}: 426655, and Na{sub 2.8}ZnIr{sub 2}O{sub 6}: 426660.) - Graphical abstract: Diffraction patterns of Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2}: neutron diffraction patterns in the main panel and synchrotron diffraction in the insets. The patterns show a small amount of ordering in the transition metal iridium layer. Display Omitted - Highlights: • We report six ternary sodium iridates with the α-NaFeO{sub 2} structure. • Compounds Na{sub 1−x}M{sub 1/3}Ir{sub 2/3}O{sub 2}, M=Co, Ni, Cu, Zn and Na{sub 1−x}M{sub 2/3}Ir{sub 1/3}O{sub 2}, M=Mn, Fe. • Rietveld refinement of powder neutron diffraction data. • All compounds are spin glasses. • NMR comparison to Na{sub 2}IrO{sub 3}.</description><subject>ABSORPTION SPECTROSCOPY</subject><subject>ANTIFERROMAGNETISM</subject><subject>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</subject><subject>INTERACTIONS</subject><subject>IRIDIUM</subject><subject>MAGNETIC SUSCEPTIBILITY</subject><subject>MAGNETIZATION</subject><subject>NEUTRON DIFFRACTION</subject><subject>NEUTRONS</subject><subject>NUCLEAR MAGNETIC RESONANCE</subject><subject>POWDERS</subject><subject>SODIUM</subject><subject>SPACE GROUPS</subject><subject>SPECIFIC HEAT</subject><subject>SPIN GLASS STATE</subject><subject>SYNCHROTRONS</subject><subject>SYNTHESIS</subject><subject>TRIGONAL LATTICES</subject><subject>X-RAY SPECTROSCOPY</subject><issn>0022-4596</issn><issn>1095-726X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNyjtOAzEQAFALgcTyuQCVJWqbmcl-SB0RRSlCsRR0kfFOhBGsV57ZIkIciotwJhoOQPWaZ8wNgkfA9m7rt32_8gS48IgesDsxFcKycR21z6emAiBydbNsz82FyBsAYnNfV2bTa5mjzoVtGAc7lTxx0cRi88H-fLtdWPPjp8wvlr6cHie2ymUM5WglD2n-sKmkISjLlTk7hHfh6z8vze364Wm1cVk07SUm5fga8zhy1D0RdTVhs_jf-gWViEQ4</recordid><startdate>20140215</startdate><enddate>20140215</enddate><creator>Baroudi, Kristen</creator><creator>Yim, Cindi</creator><creator>Wu, Hui</creator><creator>Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115</creator><creator>Huang, Qingzhen</creator><creator>Roudebush, John H.</creator><creator>Vavilova, Eugenia</creator><creator>Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan</creator><creator>Grafe, Hans-Joachim</creator><creator>Kataev, Vladislav</creator><creator>Buechner, Bernd</creator><creator>Institut für Festkörperphysik, Technische Universität Dresden, Dresden</creator><creator>Ji, Huiwen</creator><creator>Kuo, Changyang</creator><creator>Hu, Zhiwei</creator><creator>Pi, Tun-Wen</creator><creator>Pao, Chiwen</creator><creator>Lee, Jyhfu</creator><creator>Mikhailova, Daria</creator><creator>Hao Tjeng, Liu</creator><creator>Cava, R.J.</creator><scope>OTOTI</scope></search><sort><creationdate>20140215</creationdate><title>Structure and properties of α-NaFeO{sub 2}-type ternary sodium iridates</title><author>Baroudi, Kristen ; Yim, Cindi ; Wu, Hui ; Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115 ; Huang, Qingzhen ; Roudebush, John H. ; Vavilova, Eugenia ; Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan ; Grafe, Hans-Joachim ; Kataev, Vladislav ; Buechner, Bernd ; Institut für Festkörperphysik, Technische Universität Dresden, Dresden ; Ji, Huiwen ; Kuo, Changyang ; Hu, Zhiwei ; Pi, Tun-Wen ; Pao, Chiwen ; Lee, Jyhfu ; Mikhailova, Daria ; Hao Tjeng, Liu ; Cava, R.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-osti_scitechconnect_222742153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>ABSORPTION SPECTROSCOPY</topic><topic>ANTIFERROMAGNETISM</topic><topic>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</topic><topic>INTERACTIONS</topic><topic>IRIDIUM</topic><topic>MAGNETIC SUSCEPTIBILITY</topic><topic>MAGNETIZATION</topic><topic>NEUTRON DIFFRACTION</topic><topic>NEUTRONS</topic><topic>NUCLEAR MAGNETIC RESONANCE</topic><topic>POWDERS</topic><topic>SODIUM</topic><topic>SPACE GROUPS</topic><topic>SPECIFIC HEAT</topic><topic>SPIN GLASS STATE</topic><topic>SYNCHROTRONS</topic><topic>SYNTHESIS</topic><topic>TRIGONAL LATTICES</topic><topic>X-RAY SPECTROSCOPY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baroudi, Kristen</creatorcontrib><creatorcontrib>Yim, Cindi</creatorcontrib><creatorcontrib>Wu, Hui</creatorcontrib><creatorcontrib>Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115</creatorcontrib><creatorcontrib>Huang, Qingzhen</creatorcontrib><creatorcontrib>Roudebush, John H.</creatorcontrib><creatorcontrib>Vavilova, Eugenia</creatorcontrib><creatorcontrib>Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan</creatorcontrib><creatorcontrib>Grafe, Hans-Joachim</creatorcontrib><creatorcontrib>Kataev, Vladislav</creatorcontrib><creatorcontrib>Buechner, Bernd</creatorcontrib><creatorcontrib>Institut für Festkörperphysik, Technische Universität Dresden, Dresden</creatorcontrib><creatorcontrib>Ji, Huiwen</creatorcontrib><creatorcontrib>Kuo, Changyang</creatorcontrib><creatorcontrib>Hu, Zhiwei</creatorcontrib><creatorcontrib>Pi, Tun-Wen</creatorcontrib><creatorcontrib>Pao, Chiwen</creatorcontrib><creatorcontrib>Lee, Jyhfu</creatorcontrib><creatorcontrib>Mikhailova, Daria</creatorcontrib><creatorcontrib>Hao Tjeng, Liu</creatorcontrib><creatorcontrib>Cava, R.J.</creatorcontrib><collection>OSTI.GOV</collection><jtitle>Journal of solid state chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baroudi, Kristen</au><au>Yim, Cindi</au><au>Wu, Hui</au><au>Department of Materials Science and Engineering, University of Maryland, College Park, MD 20742-2115</au><au>Huang, Qingzhen</au><au>Roudebush, John H.</au><au>Vavilova, Eugenia</au><au>Zavoisky Physical Technical Institute, Russian Academy of Sciences, Kazan</au><au>Grafe, Hans-Joachim</au><au>Kataev, Vladislav</au><au>Buechner, Bernd</au><au>Institut für Festkörperphysik, Technische Universität Dresden, Dresden</au><au>Ji, Huiwen</au><au>Kuo, Changyang</au><au>Hu, Zhiwei</au><au>Pi, Tun-Wen</au><au>Pao, Chiwen</au><au>Lee, Jyhfu</au><au>Mikhailova, Daria</au><au>Hao Tjeng, Liu</au><au>Cava, R.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure and properties of α-NaFeO{sub 2}-type ternary sodium iridates</atitle><jtitle>Journal of solid state chemistry</jtitle><date>2014-02-15</date><risdate>2014</risdate><volume>210</volume><issue>1</issue><issn>0022-4596</issn><eissn>1095-726X</eissn><abstract>The synthesis, structure, and elementary magnetic and electronic properties are reported for layered compounds of the type Na{sub 3−x}MIr{sub 2}O{sub 6} and Na{sub 3−x}M{sub 2}IrO{sub 6}, where M is a transition metal from the 3d series (M=Zn, Cu, Ni, Co, Fe and Mn). The rhombohedral structures, in space group R−3m, were determined by refinement of neutron and synchrotron powder diffraction data. No clear evidence for long range 2:1 or 1:2 honeycomb-like M/Ir ordering was found in the neutron powder diffraction patterns except in the case of M=Zn, and thus in general the compounds are best designated as sodium deficient α-NaFeO{sub 2}-type phases with formulas Na{sub 1−x}M{sub 1/3}Ir{sub 2/3}O{sub 2} or Na{sub 1−x}M{sub 2/3}Ir{sub 1/3}O{sub 2}. Synchrotron powder diffraction patterns indicate that several of the compounds likely have honeycomb in-plane metal–iridium ordering with disordered stacking of the layers. All the compounds are sodium deficient under our synthetic conditions and are black and insulating. Weiss constants derived from magnetic susceptibility measurements indicate that Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2}, and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} display dominant antiferromagnetic interactions. For Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2} the dominant magnetic interactions at low temperature are ferromagnetic while at high temperatures they are antiferromagnetic; there is also a change in the effective moment. Low temperature specific heat measurements (to 2 K) on Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2} indicate the presence of a broad magnetic ordering transition. X-ray absorption spectroscopy shows that iridium is at or close to the 4+ oxidation state in all compounds. {sup 23}Na nuclear magnetic resonance measurements comparing Na{sub 2}IrO{sub 3} to Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} provide strong indications that the electron spins are short-range ordered in the latter two materials. Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}, Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2} are spin glasses. (CSD-numbers: Na{sub 0.62}Mn{sub 0.61}Ir{sub 0.39}O{sub 2}: 426657, Na{sub 0.80}Fe{sub 2/3}Ir{sub 1/3}O{sub 2}: 426659, Na{sub 0.90}Co{sub 1/3}Ir{sub 2/3}O{sub 2}: 426658, Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}: 426656, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2}: 426655, and Na{sub 2.8}ZnIr{sub 2}O{sub 6}: 426660.) - Graphical abstract: Diffraction patterns of Na{sub 0.92}Ni{sub 1/3}Ir{sub 2/3}O{sub 2}, Na{sub 0.86}Cu{sub 1/3}Ir{sub 2/3}O{sub 2} and Na{sub 0.89}Zn{sub 1/3}Ir{sub 2/3}O{sub 2}: neutron diffraction patterns in the main panel and synchrotron diffraction in the insets. The patterns show a small amount of ordering in the transition metal iridium layer. Display Omitted - Highlights: • We report six ternary sodium iridates with the α-NaFeO{sub 2} structure. • Compounds Na{sub 1−x}M{sub 1/3}Ir{sub 2/3}O{sub 2}, M=Co, Ni, Cu, Zn and Na{sub 1−x}M{sub 2/3}Ir{sub 1/3}O{sub 2}, M=Mn, Fe. • Rietveld refinement of powder neutron diffraction data. • All compounds are spin glasses. • NMR comparison to Na{sub 2}IrO{sub 3}.</abstract><cop>United States</cop><doi>10.1016/J.JSSC.2013.11.017</doi></addata></record>
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subjects ABSORPTION SPECTROSCOPY
ANTIFERROMAGNETISM
INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY
INTERACTIONS
IRIDIUM
MAGNETIC SUSCEPTIBILITY
MAGNETIZATION
NEUTRON DIFFRACTION
NEUTRONS
NUCLEAR MAGNETIC RESONANCE
POWDERS
SODIUM
SPACE GROUPS
SPECIFIC HEAT
SPIN GLASS STATE
SYNCHROTRONS
SYNTHESIS
TRIGONAL LATTICES
X-RAY SPECTROSCOPY
title Structure and properties of α-NaFeO{sub 2}-type ternary sodium iridates
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