Yang He, Chen Zezhi, Peng Ranran, Huang Haoliang, Fu Zhengping, Zhai Xiaofang, Lu Yalin
CAS Key Laboratory of Materials for Energy Conversion, Department of Materials Science and Engineering, University of Science and Technology of China Hefei 230026 P. R. China
Synergetic Innovation Center of Quantum Information & Quantum Physics, Hefei National Laboratory for Physical Sciences at Microscale, University of Science and Technology of China Hefei 230026 P. R. China.
RSC Adv. 2018 May 8;8(30):16937-16946. doi: 10.1039/c8ra02374c. eCollection 2018 May 3.
Aurivillius oxides with an intergrowth structures have been receiving increasing interest because of their special structures and potential outstanding ferroelectric properties. In this work, BiLaTiNbFeO-BiTiFeO and BiTiNbO-BiLaTiNbFeO compounds were successfully synthetised using a simple solid-state reaction method. X-Ray diffraction patterns and scanning transmission electron microscopy high angle annular dark field (STEM-HAADF) images confirm the 2-3 and the 3-4 intergrowth structures in BiTiNbO-BiLaTiNbFeO and BiLaTiNbFeO-BiTiFeO compounds, respectively. A superlattice-like distortion in these oxides was proposed resulting from the combination of sub-lattices with different and parameters, which was validated by XRD refinements and Raman spectra. Polarization-electric field tests and pulsed polarization positive-up negative-down measurements demonstrate that such superlattice-like structures can effectively enhance the intrinsic ferroelectric polarization and coercive field of these oxides, especially when compared with their component oxides BiTiNbO, BiLaTiNbFeO and BiTiFeO. Simultaneously, ferroelectric Curie temperatures of BiTiNbO-BiLaTiNbFeO and BiLaTiNbFeO-BiTiFeO oxides are lowered because of the internal stress in the superlattice-like structure. Nevertheless, the paramagnetism of the samples is hardly influenced by their structure, while mainly related to their iron content, in which iron has a similar effective magnetic moment around 3.4-3.9.
具有共生结构的奥里维利乌斯氧化物因其特殊结构和潜在的优异铁电性能而受到越来越多的关注。在本工作中,采用简单的固态反应法成功合成了BiLaTiNbFeO-BiTiFeO和BiTiNbO-BiLaTiNbFeO化合物。X射线衍射图谱和扫描透射电子显微镜高角度环形暗场(STEM-HAADF)图像分别证实了BiTiNbO-BiLaTiNbFeO和BiLaTiNbFeO-BiTiFeO化合物中的2-3和3-4共生结构。提出这些氧化物中存在一种类似超晶格的畸变,这是由具有不同晶格参数的子晶格组合导致的,XRD精修和拉曼光谱验证了这一点。极化-电场测试和脉冲极化正上负下测量表明,这种类似超晶格的结构可以有效增强这些氧化物的本征铁电极化和矫顽场,特别是与它们的组成氧化物BiTiNbO、BiLaTiNbFeO和BiTiFeO相比时。同时,由于类似超晶格结构中的内应力,BiTiNbO-BiLaTiNbFeO和BiLaTiNbFeO-BiTiFeO氧化物的铁电居里温度降低。然而,样品的顺磁性几乎不受其结构影响,而主要与其铁含量有关,其中铁的有效磁矩在3.4-3.9左右相似。