2007
DOI: 10.1007/s00269-007-0175-5
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An EPR and SQUID magnetometry study of bornite

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Cited by 23 publications
(20 citation statements)
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“…The discrepancies in earlier Mössbauer data (above and below the Neel temperature of 64-68 K) led researchers to different explanations of the nature of the magnetic properties of bornite: vacancy clustering [8,11], mixed-valence state of iron (Fe 2+ -Fe 3+ ) [9] and superparamagnetic relaxation [12]. However, the solution of this problem requires reexamination of low-temperature magnetic properties and Mössbauer parameters [13] together with other methods, and is out of the scope of the research reported here. We can prove here that the Mössbauer spectra for bornite Cu 5 FeS 4 minerals at RT point to the distortions of FeS 4 units in the structure which leads to a quadrupole splitting (Table I), unlike chalcopyrite CuFeS 2 which has no quadrupole splitting [14].…”
Section: Discussionmentioning
confidence: 99%
“…The discrepancies in earlier Mössbauer data (above and below the Neel temperature of 64-68 K) led researchers to different explanations of the nature of the magnetic properties of bornite: vacancy clustering [8,11], mixed-valence state of iron (Fe 2+ -Fe 3+ ) [9] and superparamagnetic relaxation [12]. However, the solution of this problem requires reexamination of low-temperature magnetic properties and Mössbauer parameters [13] together with other methods, and is out of the scope of the research reported here. We can prove here that the Mössbauer spectra for bornite Cu 5 FeS 4 minerals at RT point to the distortions of FeS 4 units in the structure which leads to a quadrupole splitting (Table I), unlike chalcopyrite CuFeS 2 which has no quadrupole splitting [14].…”
Section: Discussionmentioning
confidence: 99%
“…Another reason may be the dynamic spin density transfer involving the Cu 2 þ nearest to the Fe 3 þ atoms. This would cause formation of iron-copper dynamic pairs: if the exchange coupling between these two ions is antiferromagnetic in nature, this also would result in a lowering of the effective magnetic moment [24]. The most probable explanation seems to be the structural conditions in Cu 13 Fe 4 V 10 O 44 compound that cause copper ions (nominal valence 2 þ, 3d 9 , S ¼1/2) and some iron ions (nominal valence 3 þ, 3d 5 , S ¼5/2) to be magnetically silent in the investigated temperature range.…”
Section: Susceptibility and Magnetization Studymentioning
confidence: 98%
“…A very small effective magnetic moment of Cu 13 Fe 4 V 10 O 44 might have a few origins [24]. One reason may be the inaccuracy of the ionic description of the bulk magnetism in terms of conventional ionic valence states of elemental constituents.…”
Section: Susceptibility and Magnetization Studymentioning
confidence: 99%
“…Natural bornite (L-bornite) crystallizes in the orthorhombic structure with space group P bca. Two other cubic polymorphs (space group F m3m) of this mineral are known: a high temperature form (H-bornite), above 262 • C, and an intermediate temperature form (I-bornite) observed in the 200 • C to 262 • C range [1][2][3][4]. Bornite is an interesting compound because it is one of the most important ore minerals for copper [5,6].…”
Section: Introductionmentioning
confidence: 99%
“…It has special semiconducting and magnetic properties used in several high-tech materials, e.g. diluted magnetic semiconductors [3,4,7]. It shows great potential as a new economical and ecofriendly thermoelectric material.…”
Section: Introductionmentioning
confidence: 99%