Papers by Author: Hiroki Sato

Abstract: In the highly-correlated electron system Sr_1-xNd_xMnO₃ (SNMO) having the simple perovskite structure, there are interesting electronic states, which are related to degrees of charge, orbital, and spin freedoms for e_g electrons in Mn ions. Among these states, in the case of SNMO, the C-, A-and CE-type antiferromagnetic states were reported for 0.20 ≤ x ≤ 0.38, for 0.38 ≤ x ≤ 0.48, and for 0.48 ≤ x ≤ 0.52, respectively. The points to note here are that these antiferromagnetic states are directly associated with corresponding orbital orderings, and that the CE-type state also accompanies charge ordering. Because of these features, we were interested in the (A → CE) state change in SNMO. The crystallographic features of prepared SNMO samples with 0.46 ≤ x ≤ 0.50 have thus been investigated mainly by means of a transmission electron microscope equipped with a low-temperature holder. As a result, the state around 100 K for x = 0.48 was first understood to be identified as the Imma state, which includes a large number of orbital-modulated (OM) regions with an average size of about 10 nm. The feature of such regions is that the orbital modulation has an incommensurate periodicity and a charge modulation is absent in them. On the other hand, the CE-type state having the commensurate orbital and charge modulations was also confirmed to be present for x = 0.50. In addition to these two states, the state around 100 K for x = 0.46 was found to be characterized by the coexistence state consisting of the C-type orbital-ordered state and the Imma states including OM regions. In other words, the presence of the A-type orbital-ordered state could not be confirmed in the temperature range between 300 K and about 100 K for 0.46 ≤ x ≤ 0.50 in this study.

Abstract: We present a new method for soft chemical synthesis of perovskite materials. Perovskite K1-xLixNbO3 powders are produced by an ion-exchange reaction of layered perovskite precursor, K2NbO3F, with lithium chloride in water at room temperature. X-ray diffraction and X-ray fluorescent spectroscopic studies show that a mechanism of the ion-exchange reaction is a self-assembly between the perovskite nanosheets in aqueous solution.