The effects of Co-Ti co-doping on the magnetic, electrical, and magnetodielectric behaviors of M-type barium hexaferrites
Source abstract
Abstract
Magnetic, electrical and magnetodielectric properties have been studied in Co-Ti co-doped M-type hexaferrite BaCoxTixFe12-2xO19 (x = 0 ∼ 4). With the incorporation of Co-Ti, both their ferromagnetic magnetization and coercivity have been greatly changed. The temperature dependent magnetization curve shows a apparent hump at around 420 K, likely in association with more complicated cycloidal spin ordering, which is closely related to ferroelectric polarization. Interestingly, a significantly enhancement in resistivity (∼3 orders in magnitude) can be obtained in co-doped samples (x > 2), which is beneficial for magnetoelectric properties. The magnetoelectric effect were examined by dielectric tunibility under external magnetic field, which shows apparent tunability up to ∼−3% for sample with x = 2 at 1T magnetic field, further supporting it is a room temperature single phase mutliferroic material.
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Research context
OpenAlex topics: Multiferroics and related materials · Magnetic Properties and Synthesis of Ferrites · Advanced Condensed Matter Physics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
South China Normal University 1 Institute for Advanced Materials, , Guangzhou 510006, P. R. China
South China University of Technology 2 Department of Metallic Materials Science and Engineering, , Guangzhou 510640, P. R. China
Nanjing University 3 Laboratory of Solid State Microstructures, , Nanjing 210093, P. R. China
Funding
NSFC
References (25)
Show source-provided references
1. Phys. Rev. Lett. · 2005 · 94 · 13720110.1103/PhysRevLett.94.137201 ↗
2. Appl. Phys. Lett. · 2012 · 100 · 12290110.1063/1.3697636 ↗
3. Nat. Mater. · 2010 · 9 · 79710.1038/nmat2826 ↗
4. Appl. Phys. Lett. · 2012 · 100 · 03290110.1063/1.3677672 ↗
5. Appl. Phys. Lett. · 2011 · 98 · 21250410.1063/1.3593371 ↗
6. Phys. Rev. Lett. · 2010 · 105 · 25720110.1103/PhysRevLett.105.257201 ↗
7. Sci. Rep. · 2012 · 10 · 223
8. Phys. Rev. B · 2012 · 86 · 09443510.1103/PhysRevB.86.094435 ↗
9. Phys. Rev. B · 2012 · 85 · 06440210.1103/PhysRevB.85.064402 ↗
10. Nature · 2003 · 426 · 5510.1038/nature02018 ↗
11. Philips Res. Rep. · 1957 · 12 · 491
12. Ceram. Soc. · 1999 · 82 · 26910.1111/j.1551-2916.1999.tb20058.x ↗
13. J. Appl. Phys. · 2006 · 99 · 08M91110.1063/1.2165145 ↗
14. J. Phys. Chem. C · 2007 · 111 · 586610.1021/jp068955c ↗
15. J. Phys.: Condens. Matter · 2003 · 15 · 622910.1088/0953-8984/15/36/311 ↗
16. Phys. Rev. B · 2002 · 65 · 18440210.1103/PhysRevB.65.184402 ↗
17. J. Alloys Compd. · 2013 · 546 · 23410.1016/j.jallcom.2012.08.029 ↗
18. J. Magn. Magn. Mater. · 2002 · 242–245 · 140810.1016/S0304-8853(01)00963-5 ↗
19. Mater. Lett. · 2009 · 63 · 192110.1016/j.matlet.2009.06.002 ↗
20. Chem. Eng. J. · 2008 · 136 · 38310.1016/j.cej.2007.05.046 ↗
21. J. Magn. Magn. Mater. · 2001 · 224 · 1710.1016/S0304-8853(00)01355-X ↗
22. J. Appl. Phys. · 1991 · 70 · 161410.1063/1.349526 ↗
23. Solid State Commun. · 1974 · 14 · 6910.1016/0038-1098(74)90234-8 ↗
24. Appl. Phys. Lett. · 2005 · 86 · 06290310.1063/1.1862336 ↗
25. Mater. Lett. · 2002 · 55 · 35110.1016/S0167-577X(02)00391-9 ↗