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镧锰氧化物中镁替代对其结构完整性和磁行为的影响。

Impact of Mg substitution in LaMnO manganites on their structural integrity and magnetic behavior.

作者信息

Namboothiri Parvathy, K J Vishnumaya, Pham Phuong V, Supin K K, Vasundhara M

机构信息

Polymers and Functional Materials Department, CSIR-Indian Institute of Chemical Technology Hyderabad-500007 India

Academy of Scientific and Innovative Research (AcSIR) Ghaziabad-201002 India.

出版信息

RSC Adv. 2025 Mar 19;15(11):8561-8571. doi: 10.1039/d4ra08238a. eCollection 2025 Mar 17.

DOI:10.1039/d4ra08238a
PMID:40109930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11920968/
Abstract

In this study, we investigated the impact of Mg substitution at the La site in LaMnO on its structural, chemical, and magnetic properties. To explore the effects of Mg doping, we synthesized a series of compositions, La Mg MnO ( = 0.05, 0.1, 0.15, 0.2, 0.3, and 0.33), using a conventional solid-state method and systematically investigated their structural and magnetic properties. X-Ray diffraction patterns confirmed the formation of a pure rhombohedral crystal structure for the samples up to = 0.15. However, for compositions with > 0.15, the emergence of a secondary phase, MgMnO with a spinel structure, was observed alongside the primary phase. Furthermore, it was observed that the secondary phase systematically increases with increasing Mg concentration. The temperature variations in magnetic studies, measured under zero-field-cooled (ZFC) and field-cooled (FC) conditions, confirmed that the transition temperatures for all the samples were found to be below 200 K, and these temperatures were observed to decrease with increasing Mg content. Negative magnetization was observed in the low-temperature ZFC curves for the samples with > 0.2, indicating a difference in temperature-dependent magnetization due to the presence of two different structural phases. This effect became more prominent with the increase in the secondary phase, MgMnO. The magnetic studies revealed the co-existence of ferromagnetic and ferrimagnetic ordering in La Mg MnO for > 0.15 samples, while ferromagnetic ordering was retained for the samples with < 0.15, which was further corroborated by the isothermal hysteresis results.

摘要

在本研究中,我们研究了LaMnO中La位的Mg替代对其结构、化学和磁性能的影响。为了探究Mg掺杂的影响,我们采用传统的固态方法合成了一系列组成LaMgMnO(x = 0.05、0.1、0.15、0.2、0.3和0.33),并系统地研究了它们的结构和磁性能。X射线衍射图谱证实,对于x≤0.15的样品,形成了纯菱面体晶体结构。然而,对于x>0.15的组成,除了主相外,还观察到了具有尖晶石结构的第二相MgMnO的出现。此外,观察到第二相随着Mg浓度的增加而系统性增加。在零场冷却(ZFC)和场冷却(FC)条件下测量的磁性研究中的温度变化证实,所有样品的转变温度均低于200 K,并且这些温度随着Mg含量的增加而降低。对于x>0.2的样品,在低温ZFC曲线中观察到负磁化,这表明由于存在两种不同的结构相,温度依赖性磁化存在差异。随着第二相MgMnO的增加,这种效应变得更加显著。磁性研究表明,对于x>0.15的LaMgMnO样品,铁磁和亚铁磁有序共存,而对于x<0.15的样品,保留了铁磁有序,等温磁滞结果进一步证实了这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/af7a7cbe0d61/d4ra08238a-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/689d3625869e/d4ra08238a-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/a17279dc8003/d4ra08238a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/c9c2828f7ede/d4ra08238a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/f19b30e26dc0/d4ra08238a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/af7a7cbe0d61/d4ra08238a-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/689d3625869e/d4ra08238a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/f275b8915349/d4ra08238a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/a17279dc8003/d4ra08238a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/c9c2828f7ede/d4ra08238a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/11920968/f19b30e26dc0/d4ra08238a-f5.jpg
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