Synthesis, Nuclear Structure, and Magnetic Properties of some Perovskite Oxides

Abstract: Synthesis, nuclear structure, and magnetic properties of the perovskites: Nd0.7-xMgxSr0.3MnO3 (x=0.0, 0.1), Nd0.6Mg0.1Sr0.3Mn1-zMgzO3 (z=0.1, 0.2), LaCr1-yMnyO3 (y=0.0, 0.1, 0.2, 0.3) and La1-xNdxFe0.5Cr0.5O3 (x=0.1, 0.15, 0.2) have been studied. The structure of the samples was investigated by X-ray and Neutron powder diffraction and the magnetic properties were investigated by magnetization measurements using SQUID-magnetometry. All compounds have orthorhombic structure with spacegroup Pnma (No. 62).The compounds which had the composition Nd0.7Sr0.3Mn1-yMgyO3 by preparation, were found to attain the composition Nd0.7-xMgxSr0.3MnO3 and Nd0.6Mg0.1Sr0.3Mn1-zMgzO3. The x=0.0 and 0.1 compounds order in a pure ferromagnetic structure at about 200 K, but the Mn moments become slightly tilted and attain an antiferromagnetic component below 20 K. A ferromagnetic Nd moment also appears at low temperatures. The compounds with Mg substitution y=0.2 and 0.3 do not exhibit long range magnetic order, but local ferromagnetic correlations among the Mn moments appear below 200 K. At low temperature, also a local antiferromagnetic ordering of the Nd magnetic moments occurs. In these compounds, the Mn3+/Mn4+ ratio is reduced so that the double exchange interaction is suppressed and the antiferromagnetic superexchange interaction favoured.The samples of composition LaCr1-yMnyO3 have orthorhombic structure at room temperature and below. The magnetic properties of the system are markedly affected by Mn-substitution. The parent compound LaCrO3 is a pure G-type antiferromagnet with Néel temperature 290 K. With incresing Mn-substitution, a ferromagnetic component developes in the ordered phase bcause of canting of the magnetic moments. The degree of canting increases with increasing Mn-substitution and the magnitude of the antiferromagnetic component of the moment decreases. The system La1-xNdxFe0.5Cr0.5O3 has the same antiferromagnetic G-type structure as LaCrO3, but orders already at temperatures above 400 K and develops only a very weak ferromagnetic component of the magnetic moment at low temperatures.