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Ga3+^{3+}-substitution effects in the weak ferromagnetic oxide LaCo0.8_{0.8}Rh0.2_{0.2}O3_{3}

Abstract

Magnetization and x-ray diffraction have been measured on polycrystalline samples of LaCo0.8y_{0.8-y}Rh0.2_{0.2}Gay_{y}O3_{3} for 0y0.150 \leq y \leq 0.15 in order to understand the spin state of Co3+^{3+} through the Ga3+^{3+} substitution effect. The ferromagnetic order in LaCo0.8_{0.8}Rh0.2_{0.2}O3_{3} below 15 K is dramatically suppressed by the Ga3+^{3+} substitution, where the ferromagnetic volume fraction is linearly decreased. The normal state susceptibility also systematically decreases with the Ga content, from which we find that one Ga3+^{3+} ion reduces 4.6 μB\mu_{\rm B} per formula unit. We have evaluated how the concentration of the high-spin state Co3+^{3+} changes with temperature by using an extended Curie-Weiss law, and have found that the substituted Rh3+^{3+} ion stabilizes the high-spin state Co3+^{3+} ion down to low temperatures. We find that Ga3+^{3+} preferentially replaces the high-spin state Co3+^{3+}, which makes a remarkable contrast to our previous finding that Rh3+^{3+} preferentially replaces the low-spin state Co3+^{3+}. These results strongly suggest that the magnetically excited state of LaCoO3_{3} at room temperature is a mixed state of high-spin state Co3+^{3+} and low-spin state Co3+^{3+}.Comment: 5 pages, 6 figure

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