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Title: Magnetic properties of KNaMSi{sub 4}O{sub 10} compounds (M=Mn,Fe,Cu)

Journal Article · · Journal of Solid State Chemistry
;  [1]; ;  [2]
  1. CICECO and Chemistry Department, Universidade de Aveiro, 3810-193 Aveiro (Portugal)
  2. NSSD-MSTD, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6475 (United States)

In the present work the synthesis and magnetic properties of three compounds with formula KNaMSi{sub 4}O{sub 10}(M=Mn,Fe,Cu) are described. These compounds are synthetic analogs to natural occurring minerals: fenaksite-Fe{sup 2+}, litidionite-Cu{sup 2+} and manaksite-Mn{sup 2+}. The crystal structure consists of complex silicate chains interconnected by edge-sharing MO{sub 5} square pyramids dimerized in M{sub 2}O{sub 8} units. This charged metal-silicate framework is compensated by monovalent alkali metals (K{sup +}, Na{sup +}). Despite the isostructural nature of these compounds, and the consequent similarity of the M-O topology, that rules the magnetic properties, these are quite different. While there are antiferromagnetic (AF) interactions within the Mn and Cu dimers (exchange interaction J=-3.83(1) and -2.86(3)K, respectively) with no long range order, a ferromagnetic interaction within Fe dimers (J=+7.6(1)K) is observed with a three-dimensional transition at 9 K to an AF ground state. The magnetic behavior is analyzed using the HDVV (Heisenberg-Dirac-Van Vleck) formalism and discussed in the light of the crystal structure. - Magnetic susceptibility times temperature. The antiferromagnetic arrangement within Mn and Cu dimers is evident (due to the positive derivative at lower temperatures). For the Fe-counterpart a three-dimensional transition to an antiferromagnetic (AF) inter-dimer interaction is found upon cooling. Above this transition the drop in {chi}T is a signature of ferromagnetic intra-dimer interactions.

OSTI ID:
21212186
Journal Information:
Journal of Solid State Chemistry, Vol. 182, Issue 2; Other Information: DOI: 10.1016/j.jssc.2008.10.024; PII: S0022-4596(08)00516-1; Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0022-4596
Country of Publication:
United States
Language:
English