Title

Crystal Structure, Magnetic Properties, and Mössbauer Studies of La₀.₆Sr₀.₄FeO₃₋δ Prepared by Quenching in Different Atmospheres

Abstract

Samples of La0.6Sr0.4FeO3-δ compounds prepared by quenching in different gaseous environments were studied by x-ray diffraction, neutron diffraction, magnetization measurements, and Mössbauer spectroscopy (MS). All materials are single phase and crystallize in the rhombohedral perovskite structure. Samples prepared in flowing air, N2, and O2 yielded oxygen vacancies ranging from 0% to 1%. The oxygen vacancy concentration increases from 6.8% to 9.6% as the ratio of CO/CO2 changes from 10:90 to 90:10. The air-, N2-, and O2-quenched samples have a magnetic ordering temperature in the range of 300-325 K. The magnetic ordering temperature increases for all the samples subjected to the reducing CO/CO2 atmosphere. The neutron data refinements and magnetization data indicate that the Fe sublattice of La0.6Sr0.4FeO3-δ has an antiferromagnetic structure below the magnetic ordering temperature. The Fe atoms possess a magnetic moment of 3.8μB and a hyperfine field of 53 T in the CO/CO2-quenched samples. It is found that the heat treatment in the CO/CO2 atmosphere creates more oxygen vacancies, changes the Fe valence states, and increases the unit cell volume. In the meantime, the Fe-O-Fe bond angle increases. These dramatically affect the Fe-O-Fe superexchange coupling. The change of the Fe-O-Fe bond angle and the change of the Fe valence states in the CO/CO2 heat treatment play a key role in the increase of the magnetic ordering temperatures and the magnetic moment. Therefore by creating oxygen vacancies or having excess oxygen, the exchange interaction of Fe-O and the valence state of Fe ions are affected, and lead to large changes in the magnetic properties, such as the magnetic ordering temperature, the magnetic moments, and the hyperfine interactions in the pervoskite structure.

Department(s)

Physics

Second Department

Chemistry

Document Type

Article - Journal

Document Version

Citation

File Type

text

Language(s)

English

Rights

© 2002 American Physical Society (APS), All rights reserved.

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