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Crystal chemistry and magnetic properties of the K2NiF4 type diluted solid solution YCaAl1-xCrxO4 (0 ≤ x≤ 0.10) : evidence for Cr3+ clustering. / Archaimbault, F.; Choisnet, J.; Zvereva, I.

In: Materials Chemistry and Physics, Vol. 34, No. 3-4, 1993, p. 300-305.

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Archaimbault, F. ; Choisnet, J. ; Zvereva, I. / Crystal chemistry and magnetic properties of the K2NiF4 type diluted solid solution YCaAl1-xCrxO4 (0 ≤ x≤ 0.10) : evidence for Cr3+ clustering. In: Materials Chemistry and Physics. 1993 ; Vol. 34, No. 3-4. pp. 300-305.

BibTeX

@article{0ea59fac638c4fa39fb764cfe544cef2,
title = "Crystal chemistry and magnetic properties of the K2NiF4 type diluted solid solution YCaAl1-xCrxO4 (0 ≤ x≤ 0.10): evidence for Cr3+ clustering",
abstract = "The K2NiF4 type diluted solution YCa(Al1-xCrx)O4 (0 ≤ x ≤ 0.10) is studied with respect to both crystal chemistry and magnetic properties, mainly in order to obtain some evidence of Cr3+ segregation phenomena in the octahedral layers. The Al3+ → Cr3+ replacement results in a strong anisotropic variation of the cell constants in terms of an increase and a decrease in the a and c parameters, respectively, of the tetragonal cell. Such behaviour is largely dependent on the M-Oapical distances in the (Al,Cr)-O6 octahedra, as well as in the (Y,Ca)-O9 polyhedra, which show a coupling of their variation. On the basis of the temperature (80, 400 K) and Cr3+ concentration dependence of the magnetic susceptibility, which is used in the Heisenberg-Dirac-Van Vleck approach for modeling the magnetic exchange interactions, a significant deviation of the Cr3+ distribution is found with respect to a statistical distribution. The amount of Cr3+ clusters is lower than in the perovskite solid solution YAl1-xCrxO3, owing to the lower dimensionality of the K2NiF4 type structure of the YCaAl1-xCrxO4 series. The 2D character of the exchange interactions is found to be stronger than in pure chromite, YCaCrO4.",
author = "F. Archaimbault and J. Choisnet and I. Zvereva",
year = "1993",
doi = "10.1016/0254-0584(93)90051-M",
language = "English",
volume = "34",
pages = "300--305",
journal = "Materials Chemistry and Physics",
issn = "0254-0584",
publisher = "Elsevier",
number = "3-4",

}

RIS

TY - JOUR

T1 - Crystal chemistry and magnetic properties of the K2NiF4 type diluted solid solution YCaAl1-xCrxO4 (0 ≤ x≤ 0.10)

T2 - evidence for Cr3+ clustering

AU - Archaimbault, F.

AU - Choisnet, J.

AU - Zvereva, I.

PY - 1993

Y1 - 1993

N2 - The K2NiF4 type diluted solution YCa(Al1-xCrx)O4 (0 ≤ x ≤ 0.10) is studied with respect to both crystal chemistry and magnetic properties, mainly in order to obtain some evidence of Cr3+ segregation phenomena in the octahedral layers. The Al3+ → Cr3+ replacement results in a strong anisotropic variation of the cell constants in terms of an increase and a decrease in the a and c parameters, respectively, of the tetragonal cell. Such behaviour is largely dependent on the M-Oapical distances in the (Al,Cr)-O6 octahedra, as well as in the (Y,Ca)-O9 polyhedra, which show a coupling of their variation. On the basis of the temperature (80, 400 K) and Cr3+ concentration dependence of the magnetic susceptibility, which is used in the Heisenberg-Dirac-Van Vleck approach for modeling the magnetic exchange interactions, a significant deviation of the Cr3+ distribution is found with respect to a statistical distribution. The amount of Cr3+ clusters is lower than in the perovskite solid solution YAl1-xCrxO3, owing to the lower dimensionality of the K2NiF4 type structure of the YCaAl1-xCrxO4 series. The 2D character of the exchange interactions is found to be stronger than in pure chromite, YCaCrO4.

AB - The K2NiF4 type diluted solution YCa(Al1-xCrx)O4 (0 ≤ x ≤ 0.10) is studied with respect to both crystal chemistry and magnetic properties, mainly in order to obtain some evidence of Cr3+ segregation phenomena in the octahedral layers. The Al3+ → Cr3+ replacement results in a strong anisotropic variation of the cell constants in terms of an increase and a decrease in the a and c parameters, respectively, of the tetragonal cell. Such behaviour is largely dependent on the M-Oapical distances in the (Al,Cr)-O6 octahedra, as well as in the (Y,Ca)-O9 polyhedra, which show a coupling of their variation. On the basis of the temperature (80, 400 K) and Cr3+ concentration dependence of the magnetic susceptibility, which is used in the Heisenberg-Dirac-Van Vleck approach for modeling the magnetic exchange interactions, a significant deviation of the Cr3+ distribution is found with respect to a statistical distribution. The amount of Cr3+ clusters is lower than in the perovskite solid solution YAl1-xCrxO3, owing to the lower dimensionality of the K2NiF4 type structure of the YCaAl1-xCrxO4 series. The 2D character of the exchange interactions is found to be stronger than in pure chromite, YCaCrO4.

UR - http://www.scopus.com/inward/record.url?scp=0027608477&partnerID=8YFLogxK

U2 - 10.1016/0254-0584(93)90051-M

DO - 10.1016/0254-0584(93)90051-M

M3 - Article

AN - SCOPUS:0027608477

VL - 34

SP - 300

EP - 305

JO - Materials Chemistry and Physics

JF - Materials Chemistry and Physics

SN - 0254-0584

IS - 3-4

ER -

ID: 88615023