Magnetic moment directions and distributions of cations in Cr (Co) substituted spinel ferrites Ni0.7Fe2.3O4
Source abstract
Abstract
Powder samples of the spinel ferrites MxNi0.7−xFe2.3O4 (M = Cr, Co and 0.0 ≤ x ≤ 0.3) and CrxNi0.7Fe2.3−xO4 (0.0 ≤ x ≤ 0.3) were synthesized using the chemical co-precipitation method. The XRD spectra confirmed that the samples had a single-phase cubic spinel structure. Magnetic measurements showed that the magnetic moments (μexp) per formula both at 10 K and 300 K increased with Co substitution, while the values of μexp decreased with Cr substitution. Applying the assumption that the magnetic moments of Cr2+ and Cr3+ lie antiparallel to those of the divalent and trivalent Fe, Co, and Ni cations in the same sublattice of spinel ferrites, these interesting behaviors could be easily interpreted. The cation distributions of the three series of samples were estimated successfully by fitting the dependences of μexp, measured at 10 K, on the doping level x, using a quantum-mechanical potential barrier model earlier proposed by our group. The results obtained for the Cr cation distributions at the (A) and [B] sites are very close to those obtained elsewhere using neutron diffraction.
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Research context
OpenAlex topics: Magnetic Properties and Synthesis of Ferrites · Multiferroics and related materials · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Hebei Normal University 1 Hebei Advanced Thin Film Laboratory, Department of Physics, , Shijiazhuang City, 050024, People’s Republic of China
Hebei University of Engineering 2 School of Science, , Handan City, 050038, People’s Republic of China
Funding
National Natural Science Foundation of China
References (31)
Show source-provided references
1. Phys. Rev. B. · 2013 · 87 · 02441910.1103/PhysRevB.87.024419 ↗
2. Phys. Rev. B. · 2012 · 86 · 01440610.1103/PhysRevB.86.014406 ↗
3. Phys. Rev. B. · 2010 · 82 · 10411710.1103/PhysRevB.82.104117 ↗
4. Phys. Rev. B. · 2009 · 80 · 140413(R)10.1103/PhysRevB.80.140413 ↗
5. Phys. Rev. B. · 2015 · 91 · 02440710.1103/PhysRevB.91.024407 ↗
6. Phys. Rev. B. · 2015 · 91 · 05441810.1103/PhysRevB.91.054418 ↗
7. J. Appl. Phys. · 2010 · 107 · 11431010.1063/1.3429202 ↗
8. J. Magn. Magn. Mater. · 2012 · 324 · 369510.1016/j.jmmm.2012.05.050 ↗
9. Journal of Solid State Chemistry. · 2007 · 180 · 29610.1016/j.jssc.2006.10.010 ↗
10. J. Magn. Magn. Mater. · 2013 · 327 · 16710.1016/j.jmmm.2012.09.059 ↗
11. J. Alloys Compd. · 2014 · 591 · 17410.1016/j.jallcom.2013.12.180 ↗
12. Ceramics International. · 2014 · 40 · 612710.1016/j.ceramint.2013.11.064 ↗
13. J. Appl. Phys. · 2012 · 111 · 03390610.1063/1.3676438 ↗
14. J. Alloys Compd. · 2010 · 502 · 47710.1016/j.jallcom.2010.04.201 ↗
15. Solid State Commun. · 1996 · 98 · 88510.1016/0038-1098(96)00036-1 ↗
16. Physica B. · 2014 · 438 · 9110.1016/j.physb.2014.01.010 ↗
17. J. Appl. Phys. · 2014 · 116 · 12390110.1063/1.4896187 ↗
18. Chin. Phys. B. · 2014 · 23 · 10750310.1088/1674-1056/23/10/107503 ↗
19. Physica B. · 2014 · 446 · 9210.1016/j.physb.2014.04.045 ↗
20. Phys. Status Solidi B. · 2015 · 252 · 41110.1002/pssb.201451216 ↗
21. Physica B. · 2015 · 462 · 4710.1016/j.physb.2015.01.008 ↗
22. Physica B. · 2015 · 463 · 2610.1016/j.physb.2015.01.035 ↗
23. Nature. · 1992 · 358 · 13610.1038/358136a0 ↗
24. 171
25. Appl. Phys. Lett. · 2007 · 90 · 14410110.1063/1.2718507 ↗
26. Appl. Phys. Lett. · 2011 · 98 · 07251110.1063/1.3553774 ↗
27. J. Magn. Magn. Mater. · 2013 · 326 · 19710.1016/j.jmmm.2012.09.016 ↗
28. J. Alloys Compd. · 2013 · 581 · 61610.1016/j.jallcom.2013.07.153 ↗
29. J. Appl. Cryst. · 1969 · 2 · 6510.1107/S0021889869006558 ↗
30. Acta Crystallogr. A · 1976 · 32 · 75110.1107/S0567739476001551 ↗
31. Rev. Mod. Phys. · 1970 · 42 · 31710.1103/RevModPhys.42.317 ↗