{"title":"六方有序掺铬LuMn1−xCrxO3(0≤x≤0.08)锰矿的结构、振动、磁性和介电性能","authors":"Aadish Kumar Jain, Anchit Modi, Pradeep Kumar Sharma, Shubha Dubey, Ashutosh Mishra","doi":"10.1007/s10832-024-00371-z","DOIUrl":null,"url":null,"abstract":"<div><p>This study examines how controlled doping of trivalent cations (Cr<sup>3+</sup>) at manganese (Mn<sup>3+</sup>) sites influences the structural, microstructural, vibrational, magnetic, and dielectric properties of LuMn<sub>1 − x</sub>Cr<sub>x</sub>O<sub>3</sub> (0 ≤ x ≤ 0.08) compounds. These compounds were synthesized using conventional solid-state reaction techniques. Rietveld-fitted X-ray diffraction reveals hexagonal crystal symmetry (P<sub>63</sub>cm space group) with reduced lattice parameters and volume due to Cr doping and ionic size mismatch. Room temperature Raman spectra show phonon peak shifts and reduced mode intensity, indicating structural disorder or internal stress in all samples. The magnetization outcomes reveal a weak ferromagnetic property across all samples, which can be enhanced with higher concentrations of Cr ions. The frequency-dependent dielectric properties and loss tangent (tan δ) at 300 K in all examined compounds demonstrate a decrease in dielectric constant and an increase in loss tangent. These changes are attributed to the double exchange interaction between Mn<sup>3+</sup>-O-Cr<sup>3+</sup> cations, supported by the metallic character’s emergence. Our findings on improved magnetization and adjusted dielectric parameters represent progress in understanding multiferroic compounds.</p></div>","PeriodicalId":625,"journal":{"name":"Journal of Electroceramics","volume":"53 1","pages":"10 - 17"},"PeriodicalIF":1.7000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structural, vibrational, magnetic, and dielectric properties of hexagonally ordered Cr-doped LuMn1 − xCrxO3 (0 ≤ x ≤ 0.08) manganite\",\"authors\":\"Aadish Kumar Jain, Anchit Modi, Pradeep Kumar Sharma, Shubha Dubey, Ashutosh Mishra\",\"doi\":\"10.1007/s10832-024-00371-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This study examines how controlled doping of trivalent cations (Cr<sup>3+</sup>) at manganese (Mn<sup>3+</sup>) sites influences the structural, microstructural, vibrational, magnetic, and dielectric properties of LuMn<sub>1 − x</sub>Cr<sub>x</sub>O<sub>3</sub> (0 ≤ x ≤ 0.08) compounds. These compounds were synthesized using conventional solid-state reaction techniques. Rietveld-fitted X-ray diffraction reveals hexagonal crystal symmetry (P<sub>63</sub>cm space group) with reduced lattice parameters and volume due to Cr doping and ionic size mismatch. Room temperature Raman spectra show phonon peak shifts and reduced mode intensity, indicating structural disorder or internal stress in all samples. The magnetization outcomes reveal a weak ferromagnetic property across all samples, which can be enhanced with higher concentrations of Cr ions. The frequency-dependent dielectric properties and loss tangent (tan δ) at 300 K in all examined compounds demonstrate a decrease in dielectric constant and an increase in loss tangent. These changes are attributed to the double exchange interaction between Mn<sup>3+</sup>-O-Cr<sup>3+</sup> cations, supported by the metallic character’s emergence. Our findings on improved magnetization and adjusted dielectric parameters represent progress in understanding multiferroic compounds.</p></div>\",\"PeriodicalId\":625,\"journal\":{\"name\":\"Journal of Electroceramics\",\"volume\":\"53 1\",\"pages\":\"10 - 17\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Electroceramics\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10832-024-00371-z\",\"RegionNum\":4,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, CERAMICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroceramics","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s10832-024-00371-z","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, CERAMICS","Score":null,"Total":0}
Structural, vibrational, magnetic, and dielectric properties of hexagonally ordered Cr-doped LuMn1 − xCrxO3 (0 ≤ x ≤ 0.08) manganite
This study examines how controlled doping of trivalent cations (Cr3+) at manganese (Mn3+) sites influences the structural, microstructural, vibrational, magnetic, and dielectric properties of LuMn1 − xCrxO3 (0 ≤ x ≤ 0.08) compounds. These compounds were synthesized using conventional solid-state reaction techniques. Rietveld-fitted X-ray diffraction reveals hexagonal crystal symmetry (P63cm space group) with reduced lattice parameters and volume due to Cr doping and ionic size mismatch. Room temperature Raman spectra show phonon peak shifts and reduced mode intensity, indicating structural disorder or internal stress in all samples. The magnetization outcomes reveal a weak ferromagnetic property across all samples, which can be enhanced with higher concentrations of Cr ions. The frequency-dependent dielectric properties and loss tangent (tan δ) at 300 K in all examined compounds demonstrate a decrease in dielectric constant and an increase in loss tangent. These changes are attributed to the double exchange interaction between Mn3+-O-Cr3+ cations, supported by the metallic character’s emergence. Our findings on improved magnetization and adjusted dielectric parameters represent progress in understanding multiferroic compounds.
期刊介绍:
While ceramics have traditionally been admired for their mechanical, chemical and thermal stability, their unique electrical, optical and magnetic properties have become of increasing importance in many key technologies including communications, energy conversion and storage, electronics and automation. Electroceramics benefit greatly from their versatility in properties including:
-insulating to metallic and fast ion conductivity
-piezo-, ferro-, and pyro-electricity
-electro- and nonlinear optical properties
-feromagnetism.
When combined with thermal, mechanical, and chemical stability, these properties often render them the materials of choice.
The Journal of Electroceramics is dedicated to providing a forum of discussion cutting across issues in electrical, optical, and magnetic ceramics. Driven by the need for miniaturization, cost, and enhanced functionality, the field of electroceramics is growing rapidly in many new directions. The Journal encourages discussions of resultant trends concerning silicon-electroceramic integration, nanotechnology, ceramic-polymer composites, grain boundary and defect engineering, etc.