Journal of Experimental and Theoretical Physics · 2002 · 119 citations · 21 references
Natural SciencesMaterials SciencePhysicsCrystal StructureInorganic ChemistryMagnetic MaterialsMagnetic OxidesMagnetic Properties Of SolidsMagnetic SusceptibilityMagnetism In SolidsMagnetism Of Inorganic CompoundsPerovskite MaterialsMagnetic PerovskitesManganitesOxide PerovskitesOxygen Vacancy ChemistryPerovskite Crystal StructurePerovskite Oxides
The crystal structure and the magnetic and electric properties of La0.70Ba0.30MnO3 − γ manganite (0≤γ≤0.30) with a perovskite structure were studied experimentally depending on the concentration of oxygen vacancies. The stoichiometric La0.70Ba0.30MnO3 compound (γ = 0) had cubic unit cell symmetry, which did not change as oxygen deficiency increased up to γ=0.30. A decrease in the content of oxygen in the compound under study caused the occurrence of several sequential magnetic phase transitions in the ground state, from the ferromagnetic state at γ=0 through the cluster spin glass state (γ=0.15) to the antiferromagnetic state (γ=0.30) with the presence of a small ferromagnetic component. The specific electric resistance grew to become activation in character at γ=0.11, and the metal-semiconductor transition disappeared as oxygen deficiency increased. The magnetoresistance of anion-deficient compositions included (1) magnetoresistance close to the temperature of the transition to the magnetically ordered state and (2) low-temperature magnetoresistance. The magnetoresistance peak at T C disappeared as γ increased (γ=0.11), whereas the low-temperature magnetoresistance component first increased to attain a maximum of about 34% at γ=0.15 and then decreased. The results of experimental studies were used to construct a magnetic phase diagram. These results could be interpreted within the framework of superexchange magnetic ordering theory. The suggestion was made that Mn3+-O-Mn3+ indirect exchange interactions were positive in the orbitally disordered phase only when manganese was in octahedral coordination, whereas these interactions became negative if at least one of the Mn3+ ions was five-coordinate or had a smaller coordination number.
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