CEA, DSM/IRAMIS/SPCSI, F-91191 Gif-sur-Yvette Cedex, France.
Phys Rev Lett. 2012 Dec 28;109(26):267601. doi: 10.1103/PhysRevLett.109.267601. Epub 2012 Dec 26.
We measure the ferroelectric polarization of BiFeO3 films down to 3.6 nm using low energy electron and photoelectron emission microscopy. The measured polarization decays strongly below a critical thickness of 5-7 nm predicted by continuous medium theory whereas the tetragonal distortion does not change. We resolve this apparent contradiction using first-principles-based effective Hamiltonian calculations. In ultrathin films, the energetics of near open circuit electrical boundary conditions, i.e., an unscreened depolarizing field, drive the system through a phase transition from single out-of-plane polarization to nanoscale stripe domains. It gives rise to an average polarization close to zero as measured by the electron microscopy while maintaining the relatively large tetragonal distortion imposed by the nonzero polarization state of each individual domain.
我们使用低能电子和光电子发射显微镜将 BiFeO3 薄膜的铁电极化测量到 3.6nm。在连续介质理论预测的临界厚度 5-7nm 以下,测量到的极化强烈衰减,而四方畸变没有变化。我们使用基于第一性原理的有效哈密顿量计算解决了这一明显的矛盾。在超薄薄膜中,接近开路电边界条件的能量学,即未屏蔽的去极化场,通过从单轴向外极化到纳米级条纹畴的相变来驱动系统。这导致了平均极化接近于零,正如电子显微镜所测量的那样,同时保持了每个畴的非零极化状态所施加的相对较大的四方畸变。