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The synthesis of REFe0.5Cr0.5O3 (RE = La, Y) using the sol–gel method is focused and their structural differences are investigated. The results of X‐ray diffraction show that the change of ion radius at position A leads to varying degrees of octahedral distortion and spatial group structure. The scanning electron microscopy analysis reveals micron‐level particles with clear boundaries, while energy‐dispersive X‐ray spectroscopy and room temperature Mössbauer spectra indicate the presence of Fe/Cr clusters in the sample and the transitional valence of iron. Disorder in the B position leads to a saturation moment that is lower than the theoretical value. The thermomagnetic profile shows a reversal of magnetization due to the interaction between the single‐ion magnetic anisotropy and the antisymmetric Dzyaloshinskii–Moriya (DM) interaction, with a broader peak is observed due to cluster formation. The difference in negative magnetic field is due to the difference in net magnetic moment caused by different DM intensities. [ABSTRACT FROM AUTHOR]

NdFe1−xCoxO3 samples are prepared by the sol–gel method. The X‐ray diffraction (XRD) results show that these samples conform to the orthogonal perovskite structure (Pbnm), and different doping amounts can cause the patterns to shift by XRD pattern. Through the Williamson–Hall analysis, the microstrain of the lattice between different doping amounts was obtained, and the average crystal size was calculated. The element content of each sample was obtained by scanning electron microscope and energy‐dispersive X‐ray analysis. Mössbauer spectra show that different doping levels change the surrounding environment of iron, and the magnetic properties of the samples also change. [ABSTRACT FROM AUTHOR]