Van Aken Bas B, Palstra Thomas T M, Filippetti Alessio, Spaldin Nicola A
Materials Science Centre, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, The Netherland.
Nat Mater. 2004 Mar;3(3):164-70. doi: 10.1038/nmat1080. Epub 2004 Feb 22.
Understanding the ferroelectrocity in magnetic ferroelectric oxides is of both fundamental and technological importance. Here, we identify the nature of the ferroelectric phase transition in the hexagonal manganite, YMnO(3), using a combination of single-crystal X-ray diffraction, thorough structure analysis and first-principles density-functional calculations. The ferroelectric phase is characterized by a buckling of the layered MnO(5) polyhedra, accompanied by displacements of the Y ions, which lead to a net electric polarization. Our calculations show that the mechanism is driven entirely by electrostatic and size effects, rather than the usual changes in chemical bonding associated with ferroelectric phase transitions in perovskite oxides. As a result, the usual indicators of structural instability, such as anomalies in Born effective charges on the active ions, do not hold. In contrast to the chemically stabilized ferroelectrics, this mechanism for ferroelectricity permits the coexistence of magnetism and ferroelectricity, and so suggests an avenue for designing novel magnetic ferroelectrics.
理解磁性铁电氧化物中的铁电现象具有重要的基础意义和技术意义。在此,我们结合单晶X射线衍射、全面的结构分析和第一性原理密度泛函计算,确定了六方锰酸盐YMnO₃中铁电相变的本质。铁电相的特征是层状MnO₅多面体发生屈曲,并伴有Y离子的位移,从而导致净极化。我们的计算表明,该机制完全由静电和尺寸效应驱动,而非钙钛矿氧化物中铁电相变通常伴随的化学键变化。因此,诸如活性离子的玻恩有效电荷异常等结构不稳定性的常见指标并不成立。与化学稳定的铁电体不同,这种铁电机制允许磁性和铁电性共存,从而为设计新型磁性铁电体提供了一条途径。