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Hexagonal manganese oxides RMnO$_3$ show intriguing topological ferroelectric-domain walls with variable conductivity, leading to domain wall engineering. Despite the numerous experimental studies on the polar nanoscale structures, controlling ferroelectric domains has not been sufficiently investigated. Here, we reveal the unprecedented coexistence of polar-nonpolar nanoscale domains that can be formed by substituting Ti ions in HoMnO$_3$. Unusual polar nanoscale domains are embedded in nonpolar domains with different crystallographic symmetry. This polar-nonpolar coexisting structure is naturally assembled by adjusting the lattice length during a solid-state reaction process. Furthermore, the comprehensive study reveals that the reversible microstructural change with a nonpolar-polar transition is strongly correlated with the oxygen storage properties in Ho(Mn, Ti)O$_{3+\delta}$. The present results provide important insight into the nanoscale polar-nonpolar domain coexistence in functional rare-earth manganese oxides, RMnO$_3$.

Extensive studies have been performed on layered compounds, ranging from layered cuprates to van der Waals materials with critical issues of intergrowths and stacking faults. However, such structures have been studied less because of experimental difficulty. We present characteristic defect structures of intergrowths in the Ruddlesden-Popper Ca$_{2.46}$Sr$_{0.54}$Ti$_2$O$_7$, which is known to exhibit hybrid improper ferroelectricity. Transmission electron microscopy reveals that numerous intergrowths composed of 7 and 15 layers are introduced in the ferroelectric domains. Elemental maps demonstrate that Sr ions are selectively substituted into the perovskite layers of intergrowths. Density functional theory calculations support the site-selective substitution of Sr ions, favorably located in the intergrowths. The stabilization of the Ruddlesden-Popper phase and intergrowths via Sr substitution can be explained by the ionic-radius difference between Ca and Sr ions. The study reveals detailed defect structures originating from the layered perovskite structure of Ca$_{2.46}$Sr$_{0.54}$Ti$_2$O$_7$, and shows the usefulness of elemental mapping in probing the substitution effects in oxides.

Charged domain walls and boundaries in ferroelectric materials display distinct phenomena, such as an increased conductivity due to the accumulation of bound charges. Here, we report the electron microscopy observations of atomic-scale arrangements at charged domain boundaries in the hybrid improper ferroelectric Ca$_{2.46}$Sr$_{0.54}$Ti$_2$O$_7$. Like in the prototype improper ferroelectric YMnO$_3$, we find that charged domain boundaries in Ca$_{2.46}$Sr$_{0.54}$Ti$_2$O$_7$ correspond to out-of-phase boundaries, which separate adjacent domains with a fractional translational shift of the unit cell. In addition, our results show that strontium ions are located at charged domain boundaries. The out-of-phase boundary structure may decrease the polarization charge at the boundary because of the ferrielectric nature of Ca$_{2.46}$Sr$_{0.54}$Ti$_2$O$_7$, thereby promoting the stabilization of the charged state. By combining atomic-resolution imaging and density-functional theory calculations, this study proposes an unexplored stabilization mechanism of charged domain boundaries and structural defects accompanying out-of-phase translational shifts.

We investigated magnetic textures in a Sc-doped hexaferrite film by means of phase microscopy (PM) with a hole-free phase plate in a transmission electron microscope. In a zero magnetic field, the stripe-shaped magnetic domains coexist with magnetic bubbles. The magnetization in both magnetic domains was oriented perpendicular to the film and the domain walls have an in-plane magnetization. In the remnant state at 9.2 mT, several magnetic bubbles were formed with the formation of stripe-shaped magnetic domains, and the out-of-plane component in the stripe-shaped domains gradually appeared as the film thickness increased. As the film thickness increases further, the magnetic bubbles with clockwise or counter-clockwise spin helicities formed a triangular lattice. These results in the remnant state suggest that the domain wall energy in the magnetic bubble domains is lower in the thicker region.

Bloch lines are formed to reduce the magnetostatic energy generated by the Bloch walls in uniaxial magnets. Recently, it is reported that Bloch lines play important roles in the emergence and helicity reversal of magnetic bubbles in Sc-substitute M-type hexaferrites (BaFe$_{12-x-0.05}$Sc$_{x}$Mg$_{0.05}$O$_{19}$). Although Bloch lines have been discussed on the basis of micromagnetic simulations, the detailed structure was not observed directly. In this study, we investigated the microscopic structures of Bloch lines in BaFe$_{10.35}$Sc$_{1.6}$Mg$_{0.05}$O$_{19}$ uniaxial magnets. Differential-phase contrast scanning transmission microscopy (DPC-STEM) directly revealed that the edges of the Bloch walls were misaligned in the Bloch lines of BaFe$_{10.35}$Sc$_{1.6}$Mg$_{0.05}$O$_{19}$. From the micromagnetic simulations based on the Monte-Carlo technique, we showed that the misaligned Bloch walls were caused by the dipole-dipole interactions in the hexaferrite. Our results will help to understand the microstructures of Bloch lines at nanometer scale., Comment: 18 pages, 5 figures