Effect of Co–Mn Ordering on Defect-Induced Modulation of Complex Magnetic, Metamagnetic, Griffiths Phase, and Exchange Bias-like Behavior of Eu2CoMnO6

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL
Abhijit Nayak, Debasmita Bala, Athira P., Kusampal Yadav, Nasiruddin Mondal, Pranab Mandal, Venimadhav Adyam, Devajyoti Mukherjee, Bheema Lingam Chittari, Krishnamurthy Jyothinagaram
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引用次数: 0

Abstract

The double perovskite Eu2CoMnO6 (ECMO), known for its complicated metamagnetic behavior, was studied in this report to examine how postannealing synthesis affects its crystal structure and magnetic and electronic behavior. The slow-cooling, Argon treatment, and quenching procedure during the sample synthesis indicated the important significance of antisite disorder (ASD) in influencing the material’s magnetic response. The magnetic study revealed diverse transitions, including two low-temperature antiferromagnetic (AFM)-like transitions at ∼51 and ∼10 K in the slow-cooled sample and vibronic ferromagnetic (FM) superexchange interactions at ∼105 K in the argon (Ar)-treated sample, while the quenched sample displayed an AFM behavior at low temperatures. The XPS analysis indicated the presence of diverse concentrations of Co and Mn in multiple valence states, specifically (2+, 3+) and (3+, 4+) respectively, across the samples subjected to different annealing processes. The Griffiths phase was particularly noticeable in the quenched sample, highlighting the role of disorder with Griffith’s disorder exponent (λ) = 0.81. The M(H) data at 2.5 K under zero-field-cooled mode revealed that the Ar-treated sample had a smooth, saturating-like loop, while the quenched sample had the hysteresis loop shifted toward the positive field axis with a reduced magnetic moment of 2.2 μB/f.u., and the slow-cooled sample exhibited sharp metamagnetic jumps with an unsaturated magnetic moment of 3.3 μB/f.u. While M(H) data recorded under a field-cooled protocol altered the position of critical fields (HC) for the slow-cooled sample, the evolution of an extra magnetization jump was noticed in the case of the Ar-annealed sample, and the quenched sample showed the loop shifting completely toward the negative field axis. The loop shift and varying HC values were explained in terms of an exchange bias-like spin-pinning mechanism. Additionally, DFT calculations corroborate the experimental results, revealing an increased likelihood of antisite disorders in the presence of oxygen vacancies, as well as altered behavior of Co and Mn spin states in relation to the disorders and oxygen vacancies. The effect of the disorder and oxygen vacancies on the electrical and magnetic ground states was also investigated, and the results were complemented with the experimentally observed magnetic behavior. This study demonstrates how postannealing conditions may be carefully controlled to regulate the disorder and, thus, magnetic behavior, including valence states, Griffiths phase, and metamagnetic behavior of ECMO, opening up new avenues for developing materials with desired functional properties.

Abstract Image

本报告研究了以复杂的元磁行为而闻名的双包晶 Eu2CoMnO6(ECMO),以探讨退火后合成如何影响其晶体结构以及磁性和电子行为。样品合成过程中的慢冷、氩气处理和淬火程序表明,反斜长石无序(ASD)在影响材料磁响应方面具有重要意义。磁性研究揭示了多种转变,包括慢冷样品在 ∼51 K 和 ∼10 K 的两个低温反铁磁(AFM)样转变,以及氩(Ar)处理样品在 ∼105 K 的振子铁磁(FM)超交换相互作用,而淬火样品在低温下显示出 AFM 行为。XPS 分析表明,在经过不同退火处理的样品中,钴和锰分别以 (2+, 3+) 和 (3+, 4+) 的不同价态存在。格里菲斯相在淬火样品中尤为明显,突出了格里菲斯无序指数 (λ) = 0.81 的无序作用。在零场冷却模式下,2.5 K 时的 M(H) 数据显示,经过氩处理的样品具有平滑的饱和环,而淬火样品的磁滞环向正磁场轴移动,磁矩降低了 2.2 μB/f.u、在场冷却方案下记录的 M(H) 数据改变了慢冷样品的临界磁场 (HC) 位置,氩退火样品则出现了额外的磁化跃变,而淬火样品则显示磁环完全向负磁场轴移动。环向移动和不同的 HC 值可以用类似交换偏置的自旋旋进机制来解释。此外,DFT 计算也证实了实验结果,揭示了在氧空位存在的情况下,出现反位错乱的可能性增加,以及与错乱和氧空位有关的 Co 和 Mn 自旋态行为的改变。此外,还研究了无序和氧空位对电性和磁性基态的影响,其结果与实验观察到的磁性行为相辅相成。这项研究证明了如何通过仔细控制退火后条件来调节无序状态,进而调节 ECMO 的磁性行为,包括价态、格里菲斯相和元磁性行为,为开发具有所需功能特性的材料开辟了新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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