Structural Evolution and Properties of Solid Solutions of Hexagonal InMnO3 and InGaO3
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Solid solutions InMn1鈭?i>xGaxO3 (0 鈮?x 鈮?1) have been investigated using magnetic, dielectric, specific heat, differential scanning calorimetry (DSC), and high-temperature powder synchrotron X-ray diffraction (HT-SXRD) measurements. It was found that samples with 0.5 鈮?x 鈮?1 crystallize in space group P63/mmc with a 3.32 脜 and c 11.9 脜, and samples with 0.0 鈮?x 鈮?0.4 crystallize in space group P63cm with a 5.8 脜 and c 11.6 脜 at room temperature. HT-SXRD data revealed the existence of a P63cm-to-P63/mmc phase transition at about 480 K in InMn0.6Ga0.4O3 and at 950 K in InMn0.7Ga0.3O3. However, no dielectric, phonon, second-harmonic-generation, or DSC anomalies were found to be associated with these phase transitions. The phase transition should be improper ferroelectric from the symmetry point of view, but the above-mentioned experimental facts, together with the absence of ferroelectric hysteresis loops, revealed no evidence for ferroelectricity in the low-temperature P63cm structure. We suggest that InMn1鈭?i>xGaxO3 corresponds to a nonferroelectric phase of hexagonal RMnO3 with P63cm symmetry. The antiferromagnetic phase-transition temperature decreases from 118 K for x = 0 to 105 K for x = 0.1 and 73 K for x = 0.2, and no long-range magnetic ordering could be found for x 鈮?0.3. Specific heat anomalies associated with short-range magnetic ordering were observed for 0.0 鈮?x 鈮?0.5. InMn1鈭?i>xGaxO3 with small Mn contents (0.8 鈮?x 鈮?0.98) has a bright-blue color.

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