Ferromagnetic–Antiferromagnetic Coupling by Distortion of Fe/Mn Oxygen Octahedrons in (BiFeO3)m(La0.7Sr0.3MnO3)n Superlattices
Source abstract
Abstract
Interface enhanced magnetism attracts much attention due to its potential use in exploring novel structure devices. Nevertheless, the magnetic behavior at interfaces has not been quantitatively determined. In this study, abnormal magnetic moment reduction is observed in La0.7Sr0.3MnO3 (LSMO)/BiFeO3 (BFO) superlattices, which is induced by ferromagnetic (FM)/antiferromagnetic (AFM) coupling in the interface. With reduced repetition of the superlattice's unit cell [(LSMO)n/(BFO)n]60/n (n = 1, 2, 5, 10) on a SrTiO3 substrate, magnetic moment reduction from 25.5 emu cc−1 ([(LSMO)10/(BFO)10]6) to 1.5 emu cc−1 ([(LSMO)1/(BFO)1]60) is obtained. Ab initio simulations show that due to the different magnetic domain formation energies, the magnetic moment orientation tends to be paramagnetic in the FM/AFM interface. The work focuses on the magnetic domain formation energy and provides a pathway to construct artificial heterostructures that can be an effective way to tune the magnetic moment orientation and control the magnetization of ultrathin films.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Multiferroics and related materials · Magnetic and transport properties of perovskites and related materials · Advanced Condensed Matter Physics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Electronic Thin Films and Integrated Devices University of Electronic Science and Technology of China Chengdu 610054 China
Materials Science and Technology Division Los Alamos National Laboratory Los Alamos NM 87545 USA
Department of Materials Science University of Cambridge 27 Charles Babbage Road Cambridge CB3 0FS UK
Funding
U.S. Department of Energy · National Natural Science Foundation of China
References (31)
Show source-provided references
1. 10.1063/1.132986810.1063/1.1329868 ↗
2. 10.1063/1.131918310.1063/1.1319183 ↗
3. 10.1088/0957-4484/24/50/50571110.1088/0957-4484/24/50/505711 ↗
4. 10.1038/nmat280310.1038/nmat2803 ↗
5. 10.1063/1.472940810.1063/1.4729408 ↗
6. 10.1063/1.327572610.1063/1.3275726 ↗
7. Xu J. L. · J. Appl. Phys. · 2015 · 117 · 759
8. 10.1103/PhysRevLett.113.04720410.1103/PhysRevLett.113.047204 ↗
9. 10.1021/nl072617l10.1021/nl072617l ↗
10. 10.1007/BF0057602310.1007/BF00576023 ↗
11. Prinz G. A. · Science · 1999 · 283 · 330
12. 10.1126/science.280.5366.106410.1126/science.280.5366.1064 ↗
13. 10.1103/PhysRevLett.90.03680210.1103/PhysRevLett.90.036802 ↗
14. 10.1038/nature0326110.1038/nature03261 ↗
15. 10.1103/PhysRevB.92.22440510.1103/PhysRevB.92.224405 ↗
16. 10.1103/PhysRev.95.35910.1103/PhysRev.95.359 ↗
17. 10.1051/rphysap:0198000150307610010.1051/rphysap:01980001503076100 ↗
18. 10.1103/PhysRevLett.95.07720410.1103/PhysRevLett.95.077204 ↗
19. 10.1088/0022-3727/35/6/20110.1088/0022-3727/35/6/201 ↗
20. Shen X. · Appl. Phys. Lett. · 2012 · 112 · 123919
21. Zhang Q. T. · J. Appl. Phys. · 2015 · 117 · 119
22. 10.1103/PhysRevB.78.23512210.1103/PhysRevB.78.235122 ↗
23. 10.1103/PhysRevB.60.669810.1103/PhysRevB.60.6698 ↗
24. 10.1016/S0304-8853(03)00543-210.1016/S0304-8853(03)00543-2 ↗
25. 10.1063/1.309840810.1063/1.3098408 ↗
26. Tian Y. F. · Appl. Phys. Lett. · 2014 · 104 · 2404
27. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
28. 10.1103/PhysRevLett.100.13640610.1103/PhysRevLett.100.136406 ↗
29. 10.1088/0953-8984/21/39/39550210.1088/0953-8984/21/39/395502 ↗
30. 10.1103/PhysRevB.78.23520910.1103/PhysRevB.78.235209 ↗
31. 10.1063/1.12636310.1063/1.126363 ↗