Related Experiment Video
Updated: Dec 20, 2025

Visualizing Uniaxial-strain Manipulation of Antiferromagnetic Domains in Fe1+YTe Using a Spin-polarized Scanning Tunneling Microscope
Published on: March 24, 2019
Tunable magnetic anisotropy in Cr-trihalide Janus monolayers
Rehab Albaridy1, Aurelien Manchon1, Udo Schwingenschlögl1
1Physical Sciences and Engineering Division (PSE), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Researchers engineered Janus Cr-trihalide monolayers, achieving tunable magnetic anisotropy via mechanical strain. This breakthrough allows for precise control over magnetic properties, paving the way for advanced spintronic devices.
Area of Science:
- Condensed Matter Physics
- Materials Science
- Quantum Chemistry
Background:
- Tunable magnetic anisotropy in 2D materials is crucial for spintronics.
- Current 2D materials lack sufficient control over magnetic properties.
- Janus materials offer unique structural and electronic properties.
Purpose of the Study:
- Investigate the effect of mechanical strain on magnetic anisotropy in Janus Cr-trihalide monolayers.
- Explore the potential for strain-induced control of magnetic easy axis orientation.
- Assess the viability of Janus Cr-trihalides for spintronic applications.
Main Methods:
- First-principles calculations were employed.
- Simulations focused on Cr-trihalide monolayers with broken structural inversion symmetry (Janus configuration).
- The impact of biaxial compressive and tensile strain was analyzed.
Main Results:
- Magnetic anisotropy in Janus Cr-trihalides is highly sensitive to mechanical strain.
- Biaxial strain enables control over the magnetic easy axis, switching between in-plane and out-of-plane orientations.
- Compressive strain affects magnetic exchange more significantly than tensile strain.
- Ferromagnetic ordering is maintained within the studied strain range.
Conclusions:
- Janus Cr-trihalides offer a promising platform for mechanically tunable magnetism.
- Strain engineering provides a route to control magnetic anisotropy in 2D materials.
- These findings open avenues for designing next-generation spintronic and multifunctional devices.
Related Concept Videos
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...
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the involved orbitals. The...
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,...
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
Magnetic Susceptibility and Permeability
When diamagnetic materials are placed under an external magnetic field, the moments opposite to the field are induced. Hence, the susceptibility for diamagnets has a minimal negative value of 10-5–10-6. Since...

