Universal description of surface magnetism via magnetoelectric effects
- Datum
- 16.01.2025
- Zeit
- 13:00 - 15:00
- Sprecher
- Andrea Urru
- Zugehörigkeit
- Rutgers University
- Serie
- TUD nanoSeminar
- Sprache
- en
- Hauptthema
- Physik
- Andere Themen
- Physik
- Host
- Arezoo Dianat
- Beschreibung
- Due to their reduced symmetry, surfaces often host physical phenomena that are absent in the corresponding bulk material. Of particular interest for spintronics applications is the case of surfaces showing a non-vanishing magnetic dipole per unit area, named “surface magnetization” [1-2], which can occur despite the corresponding bulk being a perfectly compensated antiferromagnet with zero net magnetization. Such surface magnetization underlies intriguing physical phenomena like interfacial magnetic coupling, and can be used as a readout method of antiferromagnetic domains [3-4]. In this talk, I will first introduce a classification scheme based on whether the surface of interest is magnetically compensated or uncompensated if the bulk magnetic order is retained at the surface. Then, I will show how surface magnetization can be understood in terms of bulk magnetoelectric effects, whereby an applied electric field induces a net magnetization. The link between a bulk magnetoelectric response and surface magnetization is intuitively expected by the fact that the abrupt termination of a bulk to create a surface generates also an effective electric field at the surface. This bulk-to-boundary correspondence serves as the ground for a universal description of surface magnetization in antiferromagnets, which has been lacking thus far [5]. Finally, I will use density functional calculations to illustrate that nominally compensated surfaces in Cr2 O3 and centrosymmetric FeF 2 develop a finite magnetization at the surface, in agreement with our predictions based on the corresponding bulk magnetoelectric response. [1] K. D. Belashchenko, Phys. Rev. Lett. 105, 147204 (2010) [2] M. S. Wornle et al., Phys. Rev. B 103, 094426 (2021) [3] N. Hedrich et al., Nat. Phys. 17, 574 (2021) [4] J. Nogues and I. K. Schuller, J. Magn. Magn. Mater. 192, 203 (1999). [5] S. F. Weber, A. Urru, S. Bhowal, C. Ederer, and N. A. Spaldin, Phys. Rev. X 14, 021033 (2024).
- Links
Letztmalig verändert: 23.11.2024, 07:38:01
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TUD Materials Science - HAL (HAL Bürogebäude - 115)Hallwachsstraße301069Dresden
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TUD Institute for Materials ScienceHallwachsstr.301069Dresden
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