Hefei National Laboratory for Physical Sciences at the Microscale, Department of Physics, University of Science and Technology of China, Hefei 230026, China.
Department of Physics and Astronomy, University of Nebraska, Lincoln, NE 68588, USA.
Sci Rep. 2017 Mar 8;7:43540. doi: 10.1038/srep43540.
Here, we report the structure evolution, magnetic and ferroelectric properties in Co-doped 4- and 3-layered intergrowth Aurivillius compounds BiNdTiFeCoO-BiNdTiFeCoO. The compounds suffer a structure evolution from the parent 4-layered phase (BiNdTiFeO) to 3-layered phase (BiNdTiCoO) with increasing cobalt doping level from 0 to 1. Meanwhile the remanent magnetization and polarization show opposite variation tendencies against the doping level, and the sample with x = 0.3 has the largest remanent magnetization and the smallest polarization. It is believed that the Co concentration dependent magnetic properties are related to the population of the Fe -O-Co bonds, while the suppressed ferroelectric polarization is due to the enhanced leakage current caused by the increasing Co concentration. Furthermore, the samples (x = 0.1-0.7) with ferromagnetism show magnetoelectric coupling effects at room temperature. The results indicate that it is an effective method to create new multiferroic materials through modifying natural superlattices.
在这里,我们报告了 Co 掺杂的 4 层和 3 层相间的 Aurivillius 化合物 BiNdTiFeCoO-BiNdTiFeCoO 的结构演变、磁和铁电性能。随着钴掺杂水平从 0 增加到 1,化合物经历了从母体 4 层相(BiNdTiFeO)到 3 层相(BiNdTiCoO)的结构演变。同时,剩余磁化强度和极化表现出与掺杂水平相反的变化趋势,x=0.3 的样品具有最大的剩余磁化强度和最小的极化强度。据信,Co 浓度依赖性磁性能与 Fe-O-Co 键的分布有关,而铁电极化的抑制是由于 Co 浓度的增加导致漏电流增加所致。此外,具有铁磁性的样品(x=0.1-0.7)在室温下表现出磁电耦合效应。结果表明,通过修饰天然超晶格来创造新型多铁材料是一种有效的方法。