Reference : A structural, magnetic, and Mossbauer spectral study of several Na-Mn-Fe-bearing alluaud...
Scientific journals : Article
Physical, chemical, mathematical & earth Sciences : Earth sciences & physical geography
http://hdl.handle.net/2268/7841
A structural, magnetic, and Mossbauer spectral study of several Na-Mn-Fe-bearing alluaudites
English
Hatert, Frédéric mailto [Université de Liège - ULg > Département de géologie > Minéralogie et cristallochimie >]
Long, G. J. [> > > >]
Hautot, D. [> > > >]
Fransolet, André-Mathieu mailto [Université de Liège - ULg > Département de géologie > Minéralogie et cristallochimie >]
Delwiche, Jacques mailto [Université de Liège - ULg > Services généraux (Faculté des sciences) > Relations académiques et scientifiques (Sciences) >]
Hubin-Franskin, Marie-Jeanne mailto [Université de Liège - ULg > Département de chimie (sciences) > Chimie physique]
Grandjean, Fernande mailto [Université de Liège - ULg > Département de physique > Département de physique >]
Oct-2004
Physics and Chemistry of Minerals
Springer
31
8
487-506
Yes (verified by ORBi)
International
0342-1791
New York
[en] alluaudites ; iron phosphate ; magnetic interactions ; Mossbauer spectroscopy
[en] The synthesis and the chemical, structural, magnetic, and Mossbauer spectral characterization of three synthetic alluaudites, Na2Mn2Fe(PO4)(3), NaMn Fe-2(PO4)(3) and (Na2MnFeFeIII)-Fe-II(PO4)(3), and a natural sample with the nominal composition of NaMn Fe-2(PO4)(3), collected in the Buranga pegmatite, Rwanda, are reported. All four compounds have the expected alluaudite monoclinic C2/c structure with the general formula [A(2)A(2)'][A(1)A(1)'A(1)(2)'']M(1)M(2)(2)(PO4)(3) in which manganese(II) is on the M(1) site and manganese(II), iron(III) and, in some cases, iron(II) on the M(2) site. The X-ray structure of Na2Mn2Fe(PO4)(3) also indicates a partially disordered distribution of Na-I and Mn-II on the M(1) and A(1) crystallographic sites. All four compounds are paramagnetic above 40 K and antiferromagnetically ordered below. Above 40 K the effective magnetic moments of NaMnFe2(PO4)(3) and Na2MnFeII Fe-III(PO4)(3) are those expected of high-spin manganese(II) and iron(III) with the (6)A(1g) electronic ground state and high-spin iron(II) with the T-5(2g) electronic ground state. In contrast, the effective magnetic moment of Na2Mn2Fe(PO4)(3) is lower than expected as a result of enhanced antiferromagnetic exchange coupling by the manganese(II) on the M(2) site. The Mossbauer spectra of all four compounds have been measured from 4.2 to 295 K and have been found to be magnetically ordered below 40 K for Na2Mn2Fe(PO4)(3) and similar to35 K for the remaining compounds. The Mossbauer spectra of Na2Mn2Fe(PO4)(3) exhibit the two expected iron(III) quadrupole doublets and/or magnetic sextets expected for a random distribution of manganese(II) and iron(III) ions on the M(2) site. Further, the Mossbauer spectra of (Na2MnFeFeIII)-Fe-II(PO4)(3) exhibit the two iron(II) and two iron(III) quadrupole doublets and/or magnetic sextets expected for a random distribution of iron(II) and iron(III) on the M(2) site. Surprisingly, the synthetic and natural samples of NaMnFe2(PO4)(3) have 19 and 10% of iron(II) on the M(2) site; apparently the presence of some iron(II) stabilizes the alluaudite structure through the reduction of iron(III)-iron(III) repulsion. The temperature dependence of the iron(II) quadrupole splitting yields a 440 to 600 cm(-1) low-symmetry component to the octahedral crystal field splitting at the M(2) site. The iron(II) and iron(III) hyperfine fields observed at 4.2 K are consistent with the presence of antiferromagnetic ordering at low temperatures in all four compounds.
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http://hdl.handle.net/2268/7841

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