Related Experiment Video
Updated: Aug 23, 2025

Sputter Growth and Characterization of Metamagnetic B2-ordered FeRh Epilayers
Published on: October 5, 2013
B-Site Fe/Re Cation-Ordering Control and Its Influence on the Magnetic Properties of Sr2FeReO6 Oxide Powders
Zhuowei Wang1, Qingkai Tang1, Zhiwei Wu1
1National Laboratory of Solid State Microstructures, School of Physics, Nanjing University, Nanjing 210093, China.
Abstract:
Double-perovskite oxide Sr2FeReO6 (SFRO) powders have promising applications in spintronics due to their half-metallicity and high Curie temperature. However, their magnetic properties suffer from the existence of anti-site defects (ASDs). Here, we report on the synthesis of SFRO powders by the sol-gel process. The B-site cationic ordering degree (η) and its influence on magnetic properties are investigated. The results demonstrate that the η value is well controlled by the annealing temperature, which is as high as 85% when annealing at 1100 °C. However, the annealing atmospheres (e.g., N2 or Ar) have little effect on the η value. At room temperature, the SFRO powders crystallize in a tetragonal crystal structure (space group I4/m). They have a relatively uniform morphology and the molar ratios of Sr, Fe, and Re elements are close to 2:1:1. XPS spectra identified that Sr, Fe, and Re elements presented as Sr2+, Fe3+, and Re5+ ions, respectively, and the O element presented as O2-. The SFRO samples annealed at 1100 °C in N2, exhibiting the highest saturation magnetization (MS = 2.61 μB/f.u. at 2 K), which was ascribed to their smallest ASD content (7.45%) with an anti-phase boundary-like morphology compared to those annealed at 1000 °C (ASDs = 10.7%) or 1200 °C (ASDs = 10.95%).
More Related Videos
06:49Radio Frequency Magnetron Sputtering of GdBa2Cu3O7âˆ'ÃŽ ´/ La0.67Sr0.33MnO3 Quasi-bilayer Films on SrTiO3 STO Single-crystal Substrates
Published on: April 12, 2019
11:07Synthesis of Non-uniformly Pr-doped SrTiO3 Ceramics and Their Thermoelectric Properties
Published on: August 15, 2015
Related Concept Videos
Valence Bond Theory
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Ferromagnetism
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...