A {sup 57}Fe Moessbauer study of the cubic perovskite-type phase LaBa{sub 2}Fe{sub 3}O{sub 8+w} ({minus}0.20 < w < 0.83)
Journal Article
·
· Journal of Solid State Chemistry
- Aabo Akademi, Turku (Finland). Dept. of Physics
- Helsinki Univ. of Technology, Espoo (Finland)
- Univ. of Oslo (Norway). Dept. of Chemistry
Single-phase samples of LaBa{sub 2}Fe{sub 3}O{sub 8+w} with {minus}0.20 {le} w {le} 0.83 were synthesized, characterized by oxygen-content analyses, powder X-ray diffraction, and magnetic susceptibility, and investigated using {sup 57}Fe Moessbauer spectroscopy. At 296 K, antiferromagnetic ordering of the Fe sites was observed for samples having w {le} 0.45. When w {le} 0.45 0.0, the iron atoms occupy predominantly an Fe{sup 3+}, S = 5/2 state, the rest being Fe{sup 2+}, S = 2. For w {approx} 0, the intensities of the components in the Moessbauer spectra correspond to random distribution of oxygen vacancies around Fe{sup 3+}. When 0 {le} w {le} 0.45, increasing amounts of iron atoms enter the Fe{sup 4+}, S = 2 state. For w {ge} 0.45, which takes the paramagnetic state at room temperature, the amount of Fe{sup 4+} increases accordingly. At 85 K, there is inconclusive evidence of disproportionation of Fe{sup 4+} into Fe{sup 3+} and Fe{sup 5+} in the most oxidized w = 0.83 sample. The room-temperature Moessbauer data show that there occurs a gradual conversion from AF to P states with increasing w up to w {ge} 0.45, when all AF components simultaneously disappear. The room-temperature relationship between the average internal magnetic field and the oxygen content parameter w resembles the magnetic field vs temperature relationship for a cooperative magnetic material. The common mechanism is that both temperature and oxygen loading affect the ordered spin system.
- OSTI ID:
- 642224
- Journal Information:
- Journal of Solid State Chemistry, Journal Name: Journal of Solid State Chemistry Journal Issue: 1 Vol. 138; ISSN 0022-4596; ISSN JSSCBI
- Country of Publication:
- United States
- Language:
- English
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