Structural Stability and Properties of Marokite-Type γ‑Mn3O4

We synthesized single crystals of marokite (CaMn2O4)-type orthorhombic manganese (II,III) oxide, γ-Mn3O4, in a multianvil apparatus at pressures of 10–24 GPa. The magnetic, electronic, and optical properties of the crystals were investigated at ambient pressure. It was found that γ-Mn3O4 is a semico...

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Veröffentlicht in:Inorganic chemistry 2021-09, Vol.60 (17), p.13440-13452
Hauptverfasser: Ovsyannikov, Sergey V, Aslandukova, Alena A, Aslandukov, Andrey, Chariton, Stella, Tsirlin, Alexander A, Korobeynikov, Igor V, Morozova, Natalia V, Fedotenko, Timofey, Khandarkhaeva, Saiana, Dubrovinsky, Leonid
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container_end_page 13452
container_issue 17
container_start_page 13440
container_title Inorganic chemistry
container_volume 60
creator Ovsyannikov, Sergey V
Aslandukova, Alena A
Aslandukov, Andrey
Chariton, Stella
Tsirlin, Alexander A
Korobeynikov, Igor V
Morozova, Natalia V
Fedotenko, Timofey
Khandarkhaeva, Saiana
Dubrovinsky, Leonid
description We synthesized single crystals of marokite (CaMn2O4)-type orthorhombic manganese (II,III) oxide, γ-Mn3O4, in a multianvil apparatus at pressures of 10–24 GPa. The magnetic, electronic, and optical properties of the crystals were investigated at ambient pressure. It was found that γ-Mn3O4 is a semiconductor with an indirect band gap E g of 0.96 eV and two antiferromagnetic transitions (T N) at ∼200 and ∼55 K. The phase stability of the γ-Mn3O4 crystals was examined in the pressure range of 0–60 GPa using single-crystal X-ray diffraction and Raman spectroscopy. A bulk modulus of γ-Mn3O4 was determined to be B 0 = 235.3(2) GPa with B′ = 2.6(6). The γ-Mn3O4 phase persisted over the whole pressure range studied and did not transform or decompose upon laser heating of the sample to ∼3500 K at 60 GPa. This result seems surprising, given the high-pressure structural diversity of iron oxides with similar stoichiometries. With an increase in pressure, the degree of distortion of MnO6 polyhedra decreased. Furthermore, there are signs indicating a limited charge transfer between the Mn3+ ions in the octahedra and the Mn2+ ions in the trigonal prisms. Our results demonstrate that the high-pressure behavior of the structural, electronic, and chemical properties of manganese oxides strongly differs from that of iron oxides with similar stoichiometries.
doi_str_mv 10.1021/acs.inorgchem.1c01782
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The magnetic, electronic, and optical properties of the crystals were investigated at ambient pressure. It was found that γ-Mn3O4 is a semiconductor with an indirect band gap E g of 0.96 eV and two antiferromagnetic transitions (T N) at ∼200 and ∼55 K. The phase stability of the γ-Mn3O4 crystals was examined in the pressure range of 0–60 GPa using single-crystal X-ray diffraction and Raman spectroscopy. A bulk modulus of γ-Mn3O4 was determined to be B 0 = 235.3(2) GPa with B′ = 2.6(6). The γ-Mn3O4 phase persisted over the whole pressure range studied and did not transform or decompose upon laser heating of the sample to ∼3500 K at 60 GPa. This result seems surprising, given the high-pressure structural diversity of iron oxides with similar stoichiometries. With an increase in pressure, the degree of distortion of MnO6 polyhedra decreased. Furthermore, there are signs indicating a limited charge transfer between the Mn3+ ions in the octahedra and the Mn2+ ions in the trigonal prisms. 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Chem</addtitle><description>We synthesized single crystals of marokite (CaMn2O4)-type orthorhombic manganese (II,III) oxide, γ-Mn3O4, in a multianvil apparatus at pressures of 10–24 GPa. The magnetic, electronic, and optical properties of the crystals were investigated at ambient pressure. It was found that γ-Mn3O4 is a semiconductor with an indirect band gap E g of 0.96 eV and two antiferromagnetic transitions (T N) at ∼200 and ∼55 K. The phase stability of the γ-Mn3O4 crystals was examined in the pressure range of 0–60 GPa using single-crystal X-ray diffraction and Raman spectroscopy. A bulk modulus of γ-Mn3O4 was determined to be B 0 = 235.3(2) GPa with B′ = 2.6(6). The γ-Mn3O4 phase persisted over the whole pressure range studied and did not transform or decompose upon laser heating of the sample to ∼3500 K at 60 GPa. This result seems surprising, given the high-pressure structural diversity of iron oxides with similar stoichiometries. With an increase in pressure, the degree of distortion of MnO6 polyhedra decreased. Furthermore, there are signs indicating a limited charge transfer between the Mn3+ ions in the octahedra and the Mn2+ ions in the trigonal prisms. Our results demonstrate that the high-pressure behavior of the structural, electronic, and chemical properties of manganese oxides strongly differs from that of iron oxides with similar stoichiometries.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNo9kE9KAzEYxYMoWKtHEGbpZur3JTNJsxIR_0FLhVZwFzKZjE6dTmqSWXTnFTyL9_AQnsQpLa7e4_F4PH6EnCOMECheahNGdev8q3mzqxEaQDGmB2SAOYU0R3g5JAOA3iPn8pichLAEAMkyPiBX8-g7Ezuvm2QedVE3ddwkui2TJ-_W1sfahsRVyVR7915Hmy42a5v8fP9-fk1bNstOyVGlm2DP9jokz3e3i5uHdDK7f7y5nqQaOcRUaoms5Hklta0qPc5LW1BuwdJeKVghDFIEkZVFodFkTLAxZNSA1JjLkrEhudjtrr376GyIalUHY5tGt9Z1QdFcABMoMt5XcVftuail63zbH1MIagtLbcN_WGoPi_0BCK5iPg</recordid><startdate>20210906</startdate><enddate>20210906</enddate><creator>Ovsyannikov, Sergey V</creator><creator>Aslandukova, Alena A</creator><creator>Aslandukov, Andrey</creator><creator>Chariton, Stella</creator><creator>Tsirlin, Alexander A</creator><creator>Korobeynikov, Igor V</creator><creator>Morozova, Natalia V</creator><creator>Fedotenko, Timofey</creator><creator>Khandarkhaeva, Saiana</creator><creator>Dubrovinsky, Leonid</creator><general>American Chemical Society</general><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0988-6066</orcidid><orcidid>https://orcid.org/0000-0001-6916-8256</orcidid><orcidid>https://orcid.org/0000-0003-1027-0998</orcidid></search><sort><creationdate>20210906</creationdate><title>Structural Stability and Properties of Marokite-Type γ‑Mn3O4</title><author>Ovsyannikov, Sergey V ; Aslandukova, Alena A ; Aslandukov, Andrey ; Chariton, Stella ; Tsirlin, Alexander A ; Korobeynikov, Igor V ; Morozova, Natalia V ; Fedotenko, Timofey ; Khandarkhaeva, Saiana ; Dubrovinsky, Leonid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a160t-9a913d65f9aeffa85deb26e0e2eb220e77c121074dbba1c43738042c09a159d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ovsyannikov, Sergey V</creatorcontrib><creatorcontrib>Aslandukova, Alena A</creatorcontrib><creatorcontrib>Aslandukov, Andrey</creatorcontrib><creatorcontrib>Chariton, Stella</creatorcontrib><creatorcontrib>Tsirlin, Alexander A</creatorcontrib><creatorcontrib>Korobeynikov, Igor V</creatorcontrib><creatorcontrib>Morozova, Natalia V</creatorcontrib><creatorcontrib>Fedotenko, Timofey</creatorcontrib><creatorcontrib>Khandarkhaeva, Saiana</creatorcontrib><creatorcontrib>Dubrovinsky, Leonid</creatorcontrib><collection>MEDLINE - Academic</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ovsyannikov, Sergey V</au><au>Aslandukova, Alena A</au><au>Aslandukov, Andrey</au><au>Chariton, Stella</au><au>Tsirlin, Alexander A</au><au>Korobeynikov, Igor V</au><au>Morozova, Natalia V</au><au>Fedotenko, Timofey</au><au>Khandarkhaeva, Saiana</au><au>Dubrovinsky, Leonid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural Stability and Properties of Marokite-Type γ‑Mn3O4</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2021-09-06</date><risdate>2021</risdate><volume>60</volume><issue>17</issue><spage>13440</spage><epage>13452</epage><pages>13440-13452</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>We synthesized single crystals of marokite (CaMn2O4)-type orthorhombic manganese (II,III) oxide, γ-Mn3O4, in a multianvil apparatus at pressures of 10–24 GPa. The magnetic, electronic, and optical properties of the crystals were investigated at ambient pressure. It was found that γ-Mn3O4 is a semiconductor with an indirect band gap E g of 0.96 eV and two antiferromagnetic transitions (T N) at ∼200 and ∼55 K. The phase stability of the γ-Mn3O4 crystals was examined in the pressure range of 0–60 GPa using single-crystal X-ray diffraction and Raman spectroscopy. A bulk modulus of γ-Mn3O4 was determined to be B 0 = 235.3(2) GPa with B′ = 2.6(6). The γ-Mn3O4 phase persisted over the whole pressure range studied and did not transform or decompose upon laser heating of the sample to ∼3500 K at 60 GPa. This result seems surprising, given the high-pressure structural diversity of iron oxides with similar stoichiometries. With an increase in pressure, the degree of distortion of MnO6 polyhedra decreased. Furthermore, there are signs indicating a limited charge transfer between the Mn3+ ions in the octahedra and the Mn2+ ions in the trigonal prisms. Our results demonstrate that the high-pressure behavior of the structural, electronic, and chemical properties of manganese oxides strongly differs from that of iron oxides with similar stoichiometries.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.inorgchem.1c01782</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-0988-6066</orcidid><orcidid>https://orcid.org/0000-0001-6916-8256</orcidid><orcidid>https://orcid.org/0000-0003-1027-0998</orcidid></addata></record>
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