Studies on structural, electronic and magnetic properties of La3+ ion-substituted Ho2FeMnO6 double perovskite compounds
The advantage of exchanging lanthanides and transition metal ions make the double perovskite structured materials yield with the important prospects for the study towards applications. The double perovskite material, Ho 2 FeMnO 6 has been phase stabilized using the conventional solid-state reaction...
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Veröffentlicht in: | Journal of materials science. Materials in electronics 2021, Vol.32 (2), p.1506-1520 |
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description | The advantage of exchanging lanthanides and transition metal ions make the double perovskite structured materials yield with the important prospects for the study towards applications. The double perovskite material, Ho
2
FeMnO
6
has been phase stabilized using the conventional solid-state reaction technique. The effect of La substitution on the properties of the Ho
2
FeMnO
6
is also carried out. The structural stability of the prepared compounds is confirmed using the XPS study which confirms the oxidation states of Ho, La, Fe and Mn to be +3. Similarly, the formation of the double perovskite structure is confirmed using the Rietveld refinement of powder X-ray diffraction data by following HoFeO
3
as the starting model. The prepared compounds crystallized in orthorhombic structure with
Pbnm
space group. The La
3+
substitution marginally increases the cell volume as it has bigger ionic radius than that of Ho
3+
ion. The morphology comparison of the pure and the La-substituted Ho
2
FeMnO
6
compounds does not show any major variation. The magnetization study of Ho
2
FeMnO
6
compound reveals the antiferromagnetic property arising from the fact of Fe
3+
and Mn
3+
ions have almost similar magnitude of magnetic moment aligned anti-parallel to each other. It is further inferred that the substitution of La
3+
ions marginally reduces the magnetic response of the materials. All the characterization studies confirm that the Ho
2
FeMnO
6
double perovskite structure has been formed and the substitution of trivalent lanthanide (La
3+
) has shown with marginal effect on the physical properties of the materials. |
doi_str_mv | 10.1007/s10854-020-04920-4 |
format | Article |
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2
FeMnO
6
has been phase stabilized using the conventional solid-state reaction technique. The effect of La substitution on the properties of the Ho
2
FeMnO
6
is also carried out. The structural stability of the prepared compounds is confirmed using the XPS study which confirms the oxidation states of Ho, La, Fe and Mn to be +3. Similarly, the formation of the double perovskite structure is confirmed using the Rietveld refinement of powder X-ray diffraction data by following HoFeO
3
as the starting model. The prepared compounds crystallized in orthorhombic structure with
Pbnm
space group. The La
3+
substitution marginally increases the cell volume as it has bigger ionic radius than that of Ho
3+
ion. The morphology comparison of the pure and the La-substituted Ho
2
FeMnO
6
compounds does not show any major variation. The magnetization study of Ho
2
FeMnO
6
compound reveals the antiferromagnetic property arising from the fact of Fe
3+
and Mn
3+
ions have almost similar magnitude of magnetic moment aligned anti-parallel to each other. It is further inferred that the substitution of La
3+
ions marginally reduces the magnetic response of the materials. All the characterization studies confirm that the Ho
2
FeMnO
6
double perovskite structure has been formed and the substitution of trivalent lanthanide (La
3+
) has shown with marginal effect on the physical properties of the materials.</description><identifier>ISSN: 0957-4522</identifier><identifier>EISSN: 1573-482X</identifier><identifier>DOI: 10.1007/s10854-020-04920-4</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Antiferromagnetism ; Characterization and Evaluation of Materials ; Chemistry and Materials Science ; Crystallization ; Holmium ; Lanthanides ; Lanthanum ; Magnetic moments ; Magnetic properties ; Manganese ions ; Materials Science ; Morphology ; Optical and Electronic Materials ; Oxidation ; Perovskite structure ; Perovskites ; Physical properties ; Spectrum analysis ; Structural stability ; Substitution reactions ; Transition metals ; X ray powder diffraction</subject><ispartof>Journal of materials science. Materials in electronics, 2021, Vol.32 (2), p.1506-1520</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2021</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c249t-2719f70863910577383f49ed435ebfdf44baeeb95e8d8a9f846c4c4a12902c1f3</citedby><cites>FETCH-LOGICAL-c249t-2719f70863910577383f49ed435ebfdf44baeeb95e8d8a9f846c4c4a12902c1f3</cites><orcidid>0000-0003-1153-2881</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10854-020-04920-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10854-020-04920-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Abhirami, S.</creatorcontrib><creatorcontrib>Basha, S. Sathik</creatorcontrib><title>Studies on structural, electronic and magnetic properties of La3+ ion-substituted Ho2FeMnO6 double perovskite compounds</title><title>Journal of materials science. Materials in electronics</title><addtitle>J Mater Sci: Mater Electron</addtitle><description>The advantage of exchanging lanthanides and transition metal ions make the double perovskite structured materials yield with the important prospects for the study towards applications. The double perovskite material, Ho
2
FeMnO
6
has been phase stabilized using the conventional solid-state reaction technique. The effect of La substitution on the properties of the Ho
2
FeMnO
6
is also carried out. The structural stability of the prepared compounds is confirmed using the XPS study which confirms the oxidation states of Ho, La, Fe and Mn to be +3. Similarly, the formation of the double perovskite structure is confirmed using the Rietveld refinement of powder X-ray diffraction data by following HoFeO
3
as the starting model. The prepared compounds crystallized in orthorhombic structure with
Pbnm
space group. The La
3+
substitution marginally increases the cell volume as it has bigger ionic radius than that of Ho
3+
ion. The morphology comparison of the pure and the La-substituted Ho
2
FeMnO
6
compounds does not show any major variation. The magnetization study of Ho
2
FeMnO
6
compound reveals the antiferromagnetic property arising from the fact of Fe
3+
and Mn
3+
ions have almost similar magnitude of magnetic moment aligned anti-parallel to each other. It is further inferred that the substitution of La
3+
ions marginally reduces the magnetic response of the materials. All the characterization studies confirm that the Ho
2
FeMnO
6
double perovskite structure has been formed and the substitution of trivalent lanthanide (La
3+
) has shown with marginal effect on the physical properties of the materials.</description><subject>Antiferromagnetism</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry and Materials Science</subject><subject>Crystallization</subject><subject>Holmium</subject><subject>Lanthanides</subject><subject>Lanthanum</subject><subject>Magnetic moments</subject><subject>Magnetic properties</subject><subject>Manganese ions</subject><subject>Materials Science</subject><subject>Morphology</subject><subject>Optical and Electronic Materials</subject><subject>Oxidation</subject><subject>Perovskite structure</subject><subject>Perovskites</subject><subject>Physical properties</subject><subject>Spectrum analysis</subject><subject>Structural stability</subject><subject>Substitution reactions</subject><subject>Transition metals</subject><subject>X ray powder diffraction</subject><issn>0957-4522</issn><issn>1573-482X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kMtKQzEQhoMoWKsv4CrgUo_mdi5ZSrEqVFyo4C7k5EzkaJvUXBTf3tgK7tzMMPB_M8OH0DEl55SQ9iJS0tWiIoxURMhSxQ6a0LrllejY8y6aEFm3lagZ20cHMb4SQhrBuwn6fEh5GCFi73BMIZuUg16eYViCScG70WDtBrzSLw5SGdbBryGkDWHxQvNTPHpXxdzHNKacYMA3ns3hzt03ePC5XwIugP-Ib2MCbPxq7bMb4iHas3oZ4ei3T9HT_OpxdlMt7q9vZ5eLyjAhU8VaKm1LuoZLSuq25R23QsIgeA29HawQvQboZQ3d0GlpO9EYYYSmTBJmqOVTdLLdWx5_zxCTevU5uHJSlQO0OGB1U1JsmzLBxxjAqnUYVzp8KUrUj2C1FayKYLURrESB-BaKJexeIPyt_of6Btstf3k</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Abhirami, S.</creator><creator>Basha, S. Sathik</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F28</scope><scope>FR3</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>L7M</scope><scope>P5Z</scope><scope>P62</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>S0W</scope><orcidid>https://orcid.org/0000-0003-1153-2881</orcidid></search><sort><creationdate>2021</creationdate><title>Studies on structural, electronic and magnetic properties of La3+ ion-substituted Ho2FeMnO6 double perovskite compounds</title><author>Abhirami, S. ; Basha, S. Sathik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c249t-2719f70863910577383f49ed435ebfdf44baeeb95e8d8a9f846c4c4a12902c1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antiferromagnetism</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry and Materials Science</topic><topic>Crystallization</topic><topic>Holmium</topic><topic>Lanthanides</topic><topic>Lanthanum</topic><topic>Magnetic moments</topic><topic>Magnetic properties</topic><topic>Manganese ions</topic><topic>Materials Science</topic><topic>Morphology</topic><topic>Optical and Electronic Materials</topic><topic>Oxidation</topic><topic>Perovskite structure</topic><topic>Perovskites</topic><topic>Physical properties</topic><topic>Spectrum analysis</topic><topic>Structural stability</topic><topic>Substitution reactions</topic><topic>Transition metals</topic><topic>X ray powder diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abhirami, S.</creatorcontrib><creatorcontrib>Basha, S. Sathik</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Database (1962 - current)</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Materials Research Database</collection><collection>https://resources.nclive.org/materials</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>DELNET Engineering & Technology Collection</collection><jtitle>Journal of materials science. Materials in electronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abhirami, S.</au><au>Basha, S. Sathik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on structural, electronic and magnetic properties of La3+ ion-substituted Ho2FeMnO6 double perovskite compounds</atitle><jtitle>Journal of materials science. Materials in electronics</jtitle><stitle>J Mater Sci: Mater Electron</stitle><date>2021</date><risdate>2021</risdate><volume>32</volume><issue>2</issue><spage>1506</spage><epage>1520</epage><pages>1506-1520</pages><issn>0957-4522</issn><eissn>1573-482X</eissn><abstract>The advantage of exchanging lanthanides and transition metal ions make the double perovskite structured materials yield with the important prospects for the study towards applications. The double perovskite material, Ho
2
FeMnO
6
has been phase stabilized using the conventional solid-state reaction technique. The effect of La substitution on the properties of the Ho
2
FeMnO
6
is also carried out. The structural stability of the prepared compounds is confirmed using the XPS study which confirms the oxidation states of Ho, La, Fe and Mn to be +3. Similarly, the formation of the double perovskite structure is confirmed using the Rietveld refinement of powder X-ray diffraction data by following HoFeO
3
as the starting model. The prepared compounds crystallized in orthorhombic structure with
Pbnm
space group. The La
3+
substitution marginally increases the cell volume as it has bigger ionic radius than that of Ho
3+
ion. The morphology comparison of the pure and the La-substituted Ho
2
FeMnO
6
compounds does not show any major variation. The magnetization study of Ho
2
FeMnO
6
compound reveals the antiferromagnetic property arising from the fact of Fe
3+
and Mn
3+
ions have almost similar magnitude of magnetic moment aligned anti-parallel to each other. It is further inferred that the substitution of La
3+
ions marginally reduces the magnetic response of the materials. All the characterization studies confirm that the Ho
2
FeMnO
6
double perovskite structure has been formed and the substitution of trivalent lanthanide (La
3+
) has shown with marginal effect on the physical properties of the materials.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10854-020-04920-4</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-1153-2881</orcidid></addata></record> |
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source | Springer Journals |
subjects | Antiferromagnetism Characterization and Evaluation of Materials Chemistry and Materials Science Crystallization Holmium Lanthanides Lanthanum Magnetic moments Magnetic properties Manganese ions Materials Science Morphology Optical and Electronic Materials Oxidation Perovskite structure Perovskites Physical properties Spectrum analysis Structural stability Substitution reactions Transition metals X ray powder diffraction |
title | Studies on structural, electronic and magnetic properties of La3+ ion-substituted Ho2FeMnO6 double perovskite compounds |
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