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This work systematically investigates the spin glass behavior of the double perovskite Ca2FeReO6. Building on previous studies, we have developed a formula to quantify the ions distribution at B-site, incorporating the next-nearest neighbor interactions. Employing molecular field theory and Monte Carlo simulations, the influence of various arrangements of two B-site ions on frustration effects was uncovered. B-site is segmented into a and b-site, defining the number of nearest neighbors from Fea to Feb (and vice versa) as Zx(Zy). The significant frustration effects occur when 1

In this study, the sol-gel method synthesized the magnetic measurement and analysis of single-phase polycrystalline perovskite DyFe1-xCrxO3 (DFCO). The experimental data were fitted and calculated by a four-sublattice molecular field model. Unlike previous studies, we found that in DyFe1-xCrxO3, the spin of the A-site rare earth ion Dy3+ also changed simultaneously with the spin reorientation of the Fe3+/Cr3+ ions. The effective spin is defined as the projection of the A site's total spin on the B site's spin plane, and the curve of temperature changes is obtained after fitting. With this theory, a very accurate thermomagnetic curve is obtained by fitting. This is convincing and, at the same time, provides a reference for the development of spintronic devices in the future.

To investigate the influence of ion spin on the coupling between ferromagnetism and ferroelectricity in type II multiferroic perovskite, we prepared the multiferroic perovskite Er0.9La0.1Cr0.8Fe0.2O3 (ELCFO) using the sol-gel method, and explored the macroscopic magnetic properties of ELCFO through M\"ossbauer spectrum and magnetic testing. The thermal magnetic curve was analyzed to examine the state and change of each ionic spin in the ELCFO system at different temperature ranges, and the role of ionic spin in the coupling between ferromagnetism and ferroelectricity was investigated. This study provides a theoretical basis for further research on multiferroic perovskites and has practical implications.

Ultrafast spin control plays a pivotal role in condensed matter physics. In this study, we analyzed the macroscopic magnetization of the PrFe0.1Cr0.9O3 system by molecular field model fitting. And the whole process of system spin reorientation is accurately calculated in the fitting process. It is found that, unlike the rare-earth perovskites we have previously studied, PrFe0.1Cr0.9O3 exhibits spin-reversion properties during the reorientation process. This research will lay a theoretical foundation for precise spin control in the future., Comment: arXiv admin note: text overlap with arXiv:2207.03220

Thermally induced spin control is one of the main directions for future spin devices. In this study, we synthesized single-phase polycrystalline ErFe1-xCrxO3 and combined the magnetization curves and M\"ossbauer spectra to determine the macroscopic magnetism at room temperature. The magnetization of the system at various temperatures is well simulated by molecular field theory. And it is found that under the DM interaction, not only the B-site ions undergo a reorientation process, but the spins of the A-site ions also change at the same time. The effective spin is defined as the projection of Er3+ on the Fe3+/Cr3+ spin plane, and the whole reorientation process is obtained by fitting. This study will complement the actual process of ErFe1-xCrxO3 spin reorientation and will lay a theoretical foundation for the fabrication of future spin-controlled devices.

Understanding spin control mechanisms is an important part of condensed matter physics and the theoretical basis for designing spintronic devices. In this letter, based on four-sublattices molecular field theory, we propose that the underlying NdFe1-xCrxO3 magnetic mechanism is driven by spin reorientation sensitive to temperature. The actual coupling angular momentum, angle between the Nd3+ and Cr3+/Fe3+ moments at the given temperature is realized via the Nd3+ magnetic moment projection onto the Cr3+/Fe3+ plane. As the temperature increases, the angle between the moment of Nd3+ and the moment of Cr3+/Fe3+ decreases monotonically. In this work, the magnetic mechanism of NdFe1-xCrxO3 (x=0.1, 0.9), the close relationship between A/B angle and temperature are presented, which laid a theoretical foundation for the design of new multifunctional magnetic materials.

Sophisticated spin instruments require high-precision spin control. In this study, we accurately study the intrinsic magnetic properties of the strongly disordered system NdFe0.5Cr0.5O3 through molecular field models combined with ASD theory. The three constituent sub-magnetic phases of the system are separated, and their magnetization contributions are calculated separately. Fitting the angle of the A/B magnetic moment at a given temperature, the reorientation temperature point and temperature dependence of different magnetic phases are obtained. This research will provide a very good theoretical support for studying complex disordered systems and applying high-precision spin control and lay a foundation for the design of new functional materials.