Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/27460
Title: Synthesis and characterization of MnCrO4, a new mixed-valence antiferromagnet
Authors: Nalbandyan, V. B.
Zvereva, E. A.
Yalovega, G. E.
Shukaev, I. L.
Ryzhakova, A. P.
Guda, A. A.
Stroppa, A.
Picozzi, S.
Vasiliev, A. N.
Whangbo, M.-H.
Issue Date: 2013
Citation: Synthesis and characterization of MnCrO4, a new mixed-valence antiferromagnet / V. B. Nalbandyan, E. A. Zvereva, G. E. Yalovega [et al.] // Inorganic Chemistry. — 2013. — Vol. 52. — № 20. — P. 11850-11858.
Abstract: A new orthorhombic phase, MnCrO4, isostructural with MCrO 4 (M = Mg, Co, Ni, Cu, Cd) was prepared by evaporation of an aqueous solution, (NH4)2Cr2O7 + 2 Mn(NO 3)2, followed by calcination at 400 C. It is characterized by redox titration, Rietveld analysis of the X-ray diffraction pattern, Cr K edge and Mn K edge XANES, ESR, magnetic susceptibility, specific heat and resistivity measurements. In contrast to the high-pressure MnCrO4 phase where both cations are octahedral, the new phase contains Cr in a tetrahedral environment suggesting the charge balance Mn2+Cr 6+O4. However, the positions of both X-ray absorption K edges, the bond lengths and the ESR data suggest the occurrence of some mixed-valence character in which the mean oxidation state of Mn is higher than 2 and that of Cr is lower than 6. Both the magnetic susceptibility and the specific heat data indicate an onset of a three-dimensional antiferromagnetic order at TN ≈ 42 K, which was confirmed also by calculating the spin exchange interactions on the basis of first principles density functional calculations. Dynamic magnetic studies (ESR) corroborate this scenario and indicate appreciable short-range correlations at temperatures far above T N. MnCrO4 is a semiconductor with activation energy of 0.27 eV; it loses oxygen on heating above 400 C to form first Cr 2O3 plus Mn3O4 and then Mn 1.5Cr1.5O4 spinel. © 2013 American Chemical Society.
URI: http://elar.urfu.ru/handle/10995/27460
SCOPUS ID: 84886714574
WOS ID: 000326065600022
PURE ID: 845169
ISSN: 0020-1669
DOI: 10.1021/ic401391b
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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