1971
DOI: 10.1103/physrevb.4.3912
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Mössbauer Study of Cobalt-Zinc Ferrites

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Cited by 245 publications
(90 citation statements)
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“…Therefore, substitution of Cu by Zn in Cu 1-x Zn x Fe 2 O 4 is expected to modify the magnetic properties. The magnetization behavior and magnetic ordering of Zn-substituted Co-Zn [4], Cu-Zn [5], Ni-Zn [6], and Mg-Zn [7] ferrites have been studied by many authors. However, no detail works have been found in the literature regarding structural and hysteresis behavior of mixed Cu-Zn ferrite.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, substitution of Cu by Zn in Cu 1-x Zn x Fe 2 O 4 is expected to modify the magnetic properties. The magnetization behavior and magnetic ordering of Zn-substituted Co-Zn [4], Cu-Zn [5], Ni-Zn [6], and Mg-Zn [7] ferrites have been studied by many authors. However, no detail works have been found in the literature regarding structural and hysteresis behavior of mixed Cu-Zn ferrite.…”
Section: Introductionmentioning
confidence: 99%
“…Because of their relatively larger separation (~3.5 Å) the A-site cations are not expected to have detectable interactions with other Asite cations. In general, a B-site cation interacts though rather weakly with another B-site cation only by a direct overlap or through 90 o superexchange interaction [23]. The above depiction hints that the strongest oxygen mediated superexchange interaction is the A-O-B in comparison to the B-O-B and A-O-A arrangement.…”
Section: Magnetization Studiesmentioning
confidence: 95%
“…[33] The site assignment, from the extent of hyperfine magnetic fields in CoFe2O4, is controversial in the literature. [33][34][35][36][37] More recent studies consider that the IS values correlated with the structural data can be better used for site assignments in cobalt ferrite. Consequently, the sextet with lower IS (~ 0.19 mm s -1 , relative to -iron) is assigned to iron in tetrahedral sites (from inter-nuclear distance arguments) [35] and the sextet with higher IS (0.32 mm s -1 ) corresponds to octahedral iron sites.…”
Section: Ft-ir Spectroscopymentioning
confidence: 99%
“…In order to understand the Mössbauer results we have to remember that in AB2O4 spinels every A-site (tetrahedral) iron ion is surrounded by 12 B-site (octahedral) next nearest neighbours and each B-site iron ion is bounded by six A-site nearest neighbours. [33,34] The hyperfine parameters (isomer shift IS, quadrupole splitting ΔEQ and magnetic fields Hhf at the iron nucleus) for all Mössbauer spectra are listed in Table 1. In the computer fit, the line intensities were fixed at 3 : 2 : 1 (theoretical values) for all magnetic sublattices, the line widths were considered equal and kept fixed for all magnetic sextets and free for the central quadrupole doublet.…”
Section: Ft-ir Spectroscopymentioning
confidence: 99%