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Title: Synthesis, structure, magnetic susceptibility and Mossbauer and Raman spectroscopies of the new oxyphosphate Fe{sub 0.50}TiO(PO{sub 4})

Journal Article · · Journal of Solid State Chemistry
 [1];  [1];  [2];  [2];  [2];  [2];  [2];  [3]
  1. LCMS, UFR Sciences des Materiaux Solides, Faculte des Sciences Ben M'Sik, Casablanca (Morocco)
  2. Institut de chimie de la matiere condensee de Bordeaux (ICMCB-CNRS), 87, av. du Dr. A. Schweittzer-33608 Pessac (France)
  3. Department of Chemistry, University of Pretoria, 0002 Pretoria (South Africa)

A new iron titanyl oxyphosphate Fe{sub 0.50}TiO(PO{sub 4}) was synthesized by both solid-state reaction and Cu{sup 2+}-Fe{sup 2+} ion exchange method. The material was then characterized by X-ray diffraction, Mossbauer spectroscopy, magnetic susceptibility measurements and Raman spectroscopy. The crystal structure of the compound was refined, using X-ray powder diffraction data, by Rietveld profile method; it crytallizes in the monoclinic system, space group P2{sub 1}/c (No.14), with a=7.4039(3)A, b=7.3838(3)A, c=7.4083(3)A, {beta}=120.36{sup o}(1), V=349.44(2)A{sup 3} and Z=4. The volume of the title compound is comparable to those of the M{sub 0.50}{sup II}TiO(PO{sub 4}) series, where M{sup II}=Mg, Co, Ni and Zn. The framework is built up from [TiO{sub 6}] octahedra and [PO{sub 4}] tetrahedra. [TiO{sub 6}] octahedra are linked together by corners and form infinite chains along the c-axis. Ti atoms are displaced from the center of octahedral units showing an alternating short distance (1.73A) and a long one (2.22A). These chains are linked together by [PO{sub 4}] tetrahedra. Fe{sup 2+} cations occupy a triangle-based antiprism sharing two faces with two [TiO{sub 6}] octahedra. Mossbauer and magnetic measurements show the existence of iron only in divalent state, located exclusively in octahedral sites with high spin confition (t{sub 2g}{sup 4}e{sub g}{sup 2}). Raman study confirms the existence of Ti-O-Ti chains.

OSTI ID:
20900910
Journal Information:
Journal of Solid State Chemistry, Vol. 179, Issue 12; Other Information: DOI: 10.1016/j.jssc.2006.08.004; PII: S0022-4596(06)00455-5; Copyright (c) 2006 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