Mössbauer Spectral Evidence for Next-nearest Neighbor Interactions Within the Alluaudite Structure of Na1-xLixMnFe2(PO4)3
The Mössbauer spectra of the Na1-xLixMnFe2(PO4)3 compounds, with x = 0.00, 0.25, 0.50, and 0.75, have been measured between 90 and 295 K and analyzed in terms of a model which takes into account the next-nearest neighbor interactions within the alluaudite structure. Surprisingly, the spectra reveal an unexpected presence of iron(II) in these compounds; the amount of iron(II) is observed to decrease from 19 to 15 atomic percent of the total iron content with increasing x. The temperature dependence of the Fe2+ and Fe3+ isomer shifts agrees with that expected from a second-order Doppler shift and the resulting iron vibrating masses and Mössbauer lattice temperatures are within the expected range of values for iron cations in an octahedral environment. The temperature dependence of the Fe2+ quadrupole splitting has been fit with the Ingalls' model and the results yield a ground state orbital splitting of ca. 500 cm-1 for the iron(II) sites. The compositional dependence of the isomer shifts and Fe2+ content can be understood in terms of a decrease in the unit-cell volume with increasing substitution of sodium by lithium, a substitution which does not influence the observed quadrupole splittings.
R. P. Hermann et al., "Mössbauer Spectral Evidence for Next-nearest Neighbor Interactions Within the Alluaudite Structure of Na1-xLixMnFe2(PO4)3," Solid State Sciences, vol. 4, no. 4, pp. 507-513, Elsevier, Apr 2002.
The definitive version is available at https://doi.org/10.1016/S1293-2558(02)01278-5
Keywords and Phrases
Iron; Lithium Derivative; Sodium Derivative; Cell Volume; Chemical Composition; Chemical Structure; Isomer; Measurement; Molecular Interaction; Molecular Model; Mössbauer Spectroscopy; Structure Analysis; Temperature Dependence
International Standard Serial Number (ISSN)
Article - Journal
© 2002 Elsevier, All rights reserved.