Crystalline symmetry controlled magnetic switching in epitaxial (111) La0.7Sr0.3MnO3 thin films
Source abstract
Abstract
Mixed-valence manganite thin films are attractive for spintronic devices. Crystalline orientation is a promising route to tailor switching mechanisms, as magnetization reversal depends on the magnetic anisotropy. Here, magnetic properties of (111)-oriented La0.7Sr0.3MnO3 thin films are elucidated by correlating macroscopic and local properties. The coercive field is an order of magnitude lower than (001)-oriented La0.7Sr0.3MnO3. Locally, a 6-fold magnetic anisotropy is observed, while macroscopically, an isotropic response is prevailing. This local coupling between the symmetry of the (111)-facet and magnetization governs the domain reversal process, demonstrating that symmetry offers a route to control magnetic properties for spintronic devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Magnetic and transport properties of perovskites and related materials · Multiferroics and related materials · Advanced Condensed Matter Physics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Electronics and Telecommunications, Norwegian University of Science and Technology, Trondheim 7491, Norway
Department of Chemical Engineering and Materials Science, University of California-Davis, Davis, California 95616, USA
Department of Physics, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA
Department of Materials Science and Engineering, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA
Funding
National Science Foundation · Norwegian Research council
References (24)
Show source-provided references
1. 10.1016/0031-8914(50)90033-410.1016/0031-8914(50)90033-4 ↗
2. 10.1038/3388310.1038/33883 ↗
3. 10.1088/0022-3727/36/8/20110.1088/0022-3727/36/8/201 ↗
4. 10.1016/s0370-1573(00)00121-610.1016/s0370-1573(00)00121-6 ↗
5. 10.1063/1.153461910.1063/1.1534619 ↗
6. 10.1088/1742-6596/292/1/01200310.1088/1742-6596/292/1/012003 ↗
7. 10.1088/0022-3727/47/3/03401010.1088/0022-3727/47/3/034010 ↗
8. 10.1063/1.131677310.1063/1.1316773 ↗
9. 10.1002/pssb. 20054144710.1002/pssb. 200541447 ↗
10. 10.1103/physrevb.77.02442610.1103/physrevb.77.024426 ↗
11. 10.1063/1.169046310.1063/1.1690463 ↗
12. 10.1063/1.11945410.1063/1.119454 ↗
13. 10.1063/1.132173310.1063/1.1321733 ↗
14. 10.1063/1.350640710.1063/1.3506407 ↗
15. 10.1038/nmat322410.1038/nmat3224 ↗
16. 10.1038/nmat322510.1038/nmat3225 ↗
17. 10.1103/PhysRevB.79.10441710.1103/PhysRevB.79.104417 ↗
18. 10.1063/1.480431210.1063/1.4804312 ↗
19. 10.1063/1.360554210.1063/1.3605542 ↗
20. 10.1142/s0218625x9800163810.1142/s0218625x98001638 ↗
21. 10.1016/j.elspec.2012.03.00110.1016/j.elspec.2012.03.001 ↗
22. 10.1063/1.234789510.1063/1.2347895 ↗
23. 10.1063/1.172936710.1063/1.1729367 ↗
24. 10.1103/PhysRevB.49.1510510.1103/PhysRevB.49.15105 ↗