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首页> 外文期刊>Chemistry of Materials: A Publication of the American Chemistry Society >Observation of Stabilized Monoclinic Phase as a 'Bridge' at the Morphotropic Phase Boundary between Tetragonal Perovskite PbVO3 and Rhombohedral BiFeO3
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Observation of Stabilized Monoclinic Phase as a 'Bridge' at the Morphotropic Phase Boundary between Tetragonal Perovskite PbVO3 and Rhombohedral BiFeO3

机译:四角钙钛合作用PBVO3和菱形BIFEO3稳定单斜相的稳定单斜相作为“桥梁”

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摘要

A morphotropic phase boundary (MPB) with coexisting tetragonal and monoclinic phases was observed in perovskite-type (ABO(3)) (1 - x)PbVO3-xBiFeO(3) solid solutions that were synthesized with a high-pressure and high temperature method. At x = 0.95, the single monoclinic phase as an intermediate between tetragonal (PbVO3) and rhombohedral (BiFeO3) phases was identified by Rietveld refinement of synchrotron X-ray powder diffraction data at room temperature, and the monoclinic phase persisted in a wide temperature range. This phase also showed a polarization rotation as a function of temperature. In the tetragonal phase with 0 <= x <= 0.8, a large tetragonal distortion existed in a wide temperature range from room temperature to similar to 900 K, and it showed little dependence on temperature, indicating that the thermal stability of the perovskite structure was enhanced compared with pristine PbVO3, which decomposes at 570 K. Correspondingly, the spontaneous polarization (P-s), which originates from the hybridization between A/B site cations and oxygen, maintained a high value (>100 mu C/cm(2)) in the tetragonal phase. The present study not only provides direct evidence of a monoclinic phase acting as a "bridge" between morphotropic phases but also suggests the potential of polar perovskites with strong polarity, i.e., PbVO3, as highperformance piezoelectric materials.
机译:在Perovskite型(ABO(3))(1 - x)PBVO3-Xbifeo(3)固溶下,在具有高压和高温法合成的固溶体中观察到具有共存四方和单斜相的MOLPHOPIC相位边界(MPB) 。在x = 0.95时,通过在室温下的同步细胞改进同步细化的同步细胞细化的单晶相(BifeO3)相之间的单型单斜相均鉴定在室温下,并且在宽温度范围内持续存在单晶相。该阶段还显示出作为温度的函数的偏振旋转。在四边形相中,0 <= x <= 0.8,在宽温度范围内,从室温至类似于900 k的宽温度范围内存在大的四边形变形,并且它对温度依赖性略有依赖性,表明钙钛矿结构的热稳定性是与原始PBVO3相比增强,其在570K处分解。相应地,自发极化(PS),其源自A / B位点阳离子和氧气之间的杂交,保持高值(>100μC/ cm(2))在四边形阶段。本研究不仅提供了一种直接证据,其作为Morphotopic阶段之间的单核相阶段作为“桥梁”,而且还表明极性钙质具有强极性的极性钙酸盐,即PBVO3,作为高度的压电材料。

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