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Exotic domain-wall phenomena make ferroelectrics the candidates for nanoelectronics. The local symmetry and structure anomalies at domain walls have raised interest in the unusual functionalities, such as domain wall chirality and conductivity. Especially, the spontaneous lattice distortion and symmetry breaking at domain walls activate them as the location of structural transformation. However, the routes to achieve ferroelectric-antiferroelectric phase transition via ferroelectric domain walls remain challenging, which are important to develop materials for energy storage and conversion. Here, we have observed stepwise antiferroelectric phase transition in strained pure BiFeO3 ultrathin films derived from ferroelectric domain walls. Aberration-corrected transmission electron microscopy observation reveals that the resultant phase transition is mediated by dense 180° domain walls via providing the antiparallel cation displacement, cooperating with the enhanced interfacial oxygen octahedral clamping. First-principles calculations further confirm the critical role of interfacial oxygen octahedral coupling during this transition. These findings report an alternative route for antiferroelectric phase transition. Besides, our results provide fresh insights into functionalities of ferroelectric domain walls and open a venue for developing energy-storage materials based on domain engineering.

Retention failure is deleterious on ferroelectric domain stability, resulting in data loss in ferroelectric memories. However, the understanding of the origin of retention failure remains a challenge for the lack of a direct experimental evidence. Here, using a combination of piezoelectric force microscopy, atomic-scale scanning transmission electron microscopy and reciprocal space mapping, we report that the polarization retention failure is caused by a strain gradient induced flexoelectric field in tetragonal ferroelectric films. Atomic imaging reveals that the strain gradient is introduced by tensile strains, which is resultant from the vertically distributed Pb-rich anti-phase domains. This strain gradient couples with polarizations and results in flexoelectric fields in the films, leading to the retention failure in the films. Our study directly underlines the atomic mechanisms behind the strain gradient induced macroscopic retention failure behavior and clarifies the effect of local strain state on domain relaxation processes, thus can shed light on further understanding and improving the retention properties of oxide ferroelectrics.

Phase coexistence in ferroelectric oxide films displays complex phase competitions and transformation which suggest new multiple-coupled properties. Here we have successfully engineered the coexistence of flux-closure and a1/a2 phases in tensile-strained PbTiO3 films sandwiched between GdScO3 substrate and a SrTiO3 layer. Moreover, by using in-situ electron beam illumination, the unusual transformation from a1/a2 phase to the flux-closure phase was directly observed. In detail, there are two types of transformations: One is the nucleation, growth, and expansion of the flux-closure phase from the internal region of the a1/a2 phase. The other feature is a “dislocation gliding” like behavior: a thin lamella of a1/a2 shrinks like “partial dislocation pairs” and finally the gradually disappeared a1/a2 lamella forms a “perfect dislocation” in the flux-closure domain matrix. Phase-field simulations suggest that the a1/a2 to flux-closure transition is induced by the decrease of the depolarization field, which is screened by the injected electrons from electron beam irradiation. These results directly confirm the phase interconversion under an external stimulus at the nanometer scale, which shed new light on the fabrication of new polar textures.

A topological meron features a non-coplanar structure, whose order parameters in the core region are perpendicular to those near the perimeter. A meron is half of a skyrmion, and both have potential applications for information carrying and storage. Although merons and skyrmions in ferromagnetic materials can be readily obtained via inter-spin interactions, their behaviour and even existence in ferroelectric materials are still elusive. Here we observe using electron microscopy not only the atomic morphology of merons with a topological charge of 1/2, but also a periodic meron lattice in ultrathin PbTiO3 films under tensile epitaxial strain on a SmScO3 substrate. Phase-field simulations rationalize the formation of merons for which an epitaxial strain, as a single alterable parameter, plays a critical role in the coupling of lattice and charge. This study suggests that by engineering strain at the nanoscale it should be possible to fabricate topological polar textures, which in turn could facilitate the development of nanoscale ferroelectric devices. Merons are topological structures, but these have yet to be directly observed in ferroelectrics. Here, by epitaxially straining PbTiO3 on a SmScO3 substrate, electron microscopy and phase-field modelling allow the morphology and distribution of merons to be observed.

Ferroelectrics exhibit polarization tunable resistance switching behaviors, which are promising for next-generation non-volatile memory devices. For technological applications, thinner nanoscale arrays are expected, which feature with higher density and larger ON/OFF (RON/OFF) ratios in the metal/ferroelectrics/semiconductor heterojunction. Here, we acquire high density BiFeO3 (BFO) nano-islands around 10 nm in thickness displaying a high RON/OFF ratio of 103, comparable to the tunnel junctions. Moreover, both the macroscopic and microscopic resistive switching behaviors of the present BiFeO3 films reveal an unexpected the filamentary-type resistive switching which is modified by the charged domain walls in nano-islands dominated by the center-type domains. Particularly, the charged domain walls spontaneously formed within the BFO nano-islands are proposed as the conductive paths based on the redistribution of carriers under the applied voltages. Potential applications for memories with large RON/OFF ratios of such kind of configurable charged domain walls are demonstrated.

Manipulation of electronic states in functional ferroelectrics is promising for next generation electronics devices. The charged domain walls in ferroelectric materials especially facilitate the electronic state modulation and are promising for developing interface-based devices. However, the major challenges impeding the application are their intentional manipulation and the elusive pinning behavior. Here, results that charged domain walls in BiFeO3 films can be pinned and regulated by oxygen vacancy planar distributions controlled by oxygen pressure during film growth are reported. Using aberration-corrected scanning transmission electron microscopy complemented by theoretical simulations, rich pinning behavior of tail-to-tail charged domain walls by oxygen vacancy plates is revealed. At high annealing oxygen pressure, 71° charged domain walls are stabilized by narrow vacancy plates. Decreasing the oxygen pressure, the transformation from 71° to 109° charged domain walls happens by expanding the vacancy plates, as collaborated by phase field simulations. Besides, the 71°-109° charged domain wall pairs are stabilized due to further interaction between two neighboring vacancy plates. These results provide the active modulation of the electronic states and illuminate the rich pinning behavior of domain walls by vacancy defects in ferroelectrics, which in turn could provide implications for designing potential electronics devices.

Periodic arrays of electric dipole waves in ferroelectric oxides can be stabilized at room temperature by quenching., A dipole wave is composed of head-to-tail connected electric dipoles in the form of sine function. Potential applications in information carrying, transporting, and processing are expected, and logic circuits based on nonlinear wave interaction are promising for dipole waves. Although similar spin waves are well known in ferromagnetic materials for their roles in some physical essence, electric dipole wave behavior and even its existence in ferroelectric materials are still elusive. Here, we observe the atomic morphology of large-scale dipole waves in PbTiO3/SrTiO3 superlattice mediated by tensile epitaxial strains on scandate substrates. The dipole waves can be expressed in the formula of y = Asin (2πx/L) + y0, where the wave amplitude (A) and wavelength (L) correspond to 1.5 and 6.6 nm, respectively. This study suggests that by engineering strain at the nanoscale, it should be possible to fabricate unknown polar textures, which could facilitate the development of nanoscale ferroelectric devices.

The multiple polarization states driven by polarization rotation could trigger giant piezoelectric responses in electromechanical sensors. Theoretically and experimentally, polarization rotation in...

Domain behavior of (111)- oriented perovskite ferroelectric films is significantly different from (001)-/(101)- oriented ones, resulting in enhancing property responses such as a superior susceptibility and a reduced coercive field. However, the domain structures and evolutions with the thickness of (111)-oriented ferroelectric films, which are crucial to further understand the distinctive properties, are still obscure. In this study, the ferroelectric domains of (111)- oriented PbTiO3 films are investigated by transmission electronic microscopy (TEM) and piezoresponse force microscopy (PFM). We identify the domain evolution with the film thicknesses under anisotropic strains imposed by the orthorhombic GdScO3 (101)O substrates. Contrast analysis and electron diffraction patterns reveal that only four ferroelectric variants evolve in PTO films: d2+, d2-, d3+ and d3-, with the polarization directions along [010], [0 1 ¯ 0], [001] and [00 1 ¯ ], respectively. Two kinds of domain walls are formed: “inclined” (011) domain walls for d2-/d3+ (d2+/d3-) domains, “normal” (01 1 ¯ ) domain walls for d2-/d3+ (d2+/d3-) domains. The width of periodically distributed d2+/d3+ (d2-/d3-) domains increases with film thickness following the square root rule. Aberration-corrected scanning transmission electronic microscopy demonstrates the lattice characteristics of domains in (111)- oriented PbTiO3 films are consistent with tetragonal ferroelectric domains. PFM studies reveal that both the out-of-plane and in-plane polarization components of d2-/d3+ (d2+/d3-) domains are non-identical, whereas the d2+/d3+ (d2-/d3-) domains possess uniform out-of-plane polarization component and non-uniform in-plane polarization component. This study discloses the domain structure in (111)- oriented tetragonal ferroelectric films under anisotropic strains and the association with the ferroelectric properties.

Topological defects showing exotic properties and diverse functionalities provide us a potential utilization in nanoscale electronic devices. However, the formation mechanism and density manipulati...

Controlling domain width, orientation, and patterns in oxide ferroelectrics are not only important for fundamental research but also for potential electronic application. Here, a series of PbTiO3 thin films under various cooling rates were deposited on (110)-oriented NdScO3 substrates by pulsed laser deposition and investigated by using conventional transmission electron microscopy, Cs-corrected scanning TEM and piezoresponse force microscopy. Contrast analysis and electron diffraction revealed that PbTiO3 films are a1/a2 domain patterns under large tensile strains with different cooling rates. The a1/a2 domains distribute periodically and the domain width increases with decrease in the cooling rates. Upon increasing the cooling rate, the domain density increases and the domain configurations become complicated. There are special square frame-like domain patterns with charged domain walls found in the PTO films with the fast cooling rate. PFM measurement shows that the PTO films with high cooling rate exhibit enhanced piezoresponse behavior which is ascribed to the high density domain/domain walls and special domain configurations. The formation mechanism of the different domain configurations is discussed in terms of the effect of cooling rates, defects and thermal kinetics. These results are expected to provide useful information for domain/domain wall control and thus facilitate further modulation of the properties for potential applications.

Common pursuits of developing nanometric logic and neuromorphic applications have motivated intensive research studies into low-dimensional resistive random-access memory (RRAM) materials. However, fabricating resistive switching medium with inherent stability and homogeneity still remains a bottleneck. Herein, we report a self-assembled uniform biphasic system, comprising low-resistance 3 nm-wide (Bi0.4,La0.6)FeO3-δ nanosheets coherently embedded in a high-resistance (Bi0.2,La0.8)FeO3-δ matrix, which were spinodally decomposed from an overall stoichiometry of the (Bi0.24,La0.76)FeO3-δ parent phase, as a promising nanocomposite to be a stable and endurable RRAM medium. The Bi-rich nanosheets accommodating high concentration of oxygen vacancies as corroborated by X-ray photoelectron spectroscopy and electron energy loss spectroscopy function as fast carrier channels, thus enabling an intrinsic electroforming-free character. Surficial electrical state and resistive switching properties are investigated using multimodal scanning probe microscopy techniques and macroscopic I-V measurements, showing high on/off ratio (∼103) and good endurance (up to 1.6 × 104 cycles). The established spinodal decomposition-driven phase-coexistence BLFO system demonstrates the merits of stability, uniformity, and endurability, which is promising for further application in RRAM devices.

High-index ferroelectric thin films show excellent dielectricity, piezoelectricity and switching behaviors. Understanding the misfit strain relaxation behavior may prove beneficial to gaining insights into the high-quality growth of high-index ferroelectric films. In this study, ferroelectric PbTiO3 thin films were deposited on the (101)-oriented (La, Sr)(Al, Ta)O3 substrate by pulsed laser deposition and were investigated using (scanning) transmission electron microscopy. Two types of misfit dislocations with line directions of and [010] were found at the interface. The dislocation exhibited Burgers vectors of a [011] or [01 $\overline{1}$ 1], while the [010] dislocation featured Burgers vectors of a[ $\overline{1}$ 01]. The former might be generated by gliding, and the latter by climbing. We propose that the misfit strain relaxation in this film system basically results from the formation of dislocations and the residual misfit strain is relaxed via the formation of 90° ac domains.

Strongly correlated oxides exhibit multiple degrees of freedoms, which can potentially mediate exotic phases with exciting physical properties, such as the polar vortex recently found in ferroelectric oxide films. A polar vortex is stabilized by competition between charge, lattice, and/or orbital degrees of freedom, which displays vortex–ferroelectric phase transitions and emergent chirality, making it a potential candidate for designing information storage and processing devices. Here, by a combination of controlled film growth and aberration-corrected scanning transmission electron microscopy, we obtain nanoscale vortex arrays in [110]-oriented BiFeO3 films. These vortex arrays are stabilized in ultrathin BiFeO3 layers sandwiched by two coherently grown orthorhombic scandate layers, exhibiting a ferroelectric morphotropic phase boundary constituted by a mixed-phase structure of polar orthorhombic BiFeO3 and rhombohedral BiFeO3. Clear polarization switching and piezoelectric signals were observed in thes...

High-index ferroelectric films as (101)-orientated ones exhibit enhanced dielectric responses, piezoelectric responses, and exotic ferroelectric switching behaviors, which are potential candidates for applications in memories and capacitors. However, possible domain patterns and domain wall structures in (101)-oriented ferroelectric thin films are still elusive, which results in difficulties in understanding the origin and further modulating their special properties. In this work, a series of PbTiO3 (PTO) thin films with 35, 50, 60, and 70 nm in thickness were grown on (101)-oriented (LaAlO3)0.29(SrTa1/2Al1/2O3)0.71 (LSAT(101)) substrates by pulsed laser deposition and investigated by both piezoresponse force microscopy (PFM) and (scanning) transmission electron microscopy ((S)TEM). PFM measurements reveal that periodic stripe domains are dominant in 50 nm thick PTO films. Besides stripe domains, a/c domains appear in films with thickness more than 60 nm. A thickness-dependent evolution of piezoresponse a...

Flexoelectricity has been shown to be an effective strategy to modulate the polarization configurations, domain structures, and physical properties in nanoscale ferroelectric thin films. However, the relations between the domain switching processes and flexoelectric effects remain elusive, which is essential for the design of nanoscale ferroelectric electric devices. In this work, strain-gradient and normal PbTiO3 films are fabricated and investigated to resolve this elusive relationship. By using large-scale and local piezoelectric force microscopy characterization, the ferroelectric domain switching in strain-gradient PbTiO3 films is found to be hard and hindered under applied electric fields compared with the normal ones. Successive atomic-scale scanning transmission electron microscopy imaging analysis manifests that the domains in the strain-gradient PbTiO3 films are stabilized by an additional effective strain gradient-induced flexoelectric field, which was introduced by negative pressure originated from vertically distributed Pb-rich anti-phase domains. This study proposes an effective method to stabilize the ferroelectric polarization in nanoscale ferroelectric films, thus facilitate improving the reliability of ferroelectric electronic devices.

Large compressive strains may introduce giant tetragonality and morphotropic phase boundaries in perovskite BiFeO3 films, where the coexisting tetragonal and rhombohedral phases (T like and R like phases) are identified to exhibit large piezoelectric response. Here, we have further achieved mechanical bending deformations in R like BiFeO3 through its neighboring T like BiFeO3 phases, where a strain gradient of ∼106/m was identified. Aberration-corrected scanning transmission electron microscopy revealed not only the strain distributions but also the atomic scale Fe polar displacement in the gradient R like BiFeO3. In spite of the giant strain gradient, the polarization direction in each R like BiFeO3 unit cell was found mainly along its diagonal direction, suggesting that potential flexoelectric coupling induced polarization in BiFeO3 is smaller than its spontaneous polarizations, while a large built-in electric field can be obtained via the large strain gradient. Our results indicate that the common phase coexistences in oxide materials could be further manipulated to introduce elastic strain gradients and tune the properties for oxide films.

Giant piezoelectricity has been thought to be originated from polarization rotation, electric-field-induced phase transformation or nano-domain reorientation in diverse complicated morphotropic phase boundaries (MPB) based piezoelectric ceramics. However, the deterministic contribution to the peak piezoelectricity is still elusive. Here, a full stage of piezoelectric response is presented in pure PbTiO3 films epitaxially constrained as the monoclinic phase on SrTiO3(111), where the as-prepared films feature complicated monoclinic nano-domains with {201} domain boundaries. By applying external voltage, the piezoelectric response undergoes three distinct stages which correspond, respectively, to the three existing mechanisms in terms of polarization rotation, nano-domain reorientation, and electric-field-induced phase transformation. A direct correlation between the electric-poling process and the piezoelectric response is established, confirming that the phase transformation from the monoclinic to tetragonal plays a dominant role for the superior piezoelectric properties of the oxide. This study clarifies the role of monoclinic phase by integrating the three individual mechanisms of piezoresponse into a single-phase perovskite oxide, which may facilitate the development of high-performance piezoelectric materials for electronic device applications.

It is known that high-index perovskite ferroelectric thin films exhibit giant permittivity, piezoelectric response, and a particular switching behavior. However, the fine domain configuration in high-index ferroelectric films is not yet clarified, which triggers difficulties to further modulate their electric properties. In this work, we focus on the tetragonal PbTiO3 thin films with thicknesses of 20, 40, 55, and 70 nm deposited on a [101]-oriented KTaO3 substrate. By using piezoresponse force microscopy and state-of-the-art scanning transmission electron microscopy, the stripe a/c domains with alternately wide c and narrow a domains are observed in all these PbTiO3 films. The periodic stripe a/c domains with {101} domain walls extend along the in-plane [ 11 1 ¯ ] or [ 1 1 ¯ 1 ¯ ] direction, which almost completely relaxes the misfit strain between the PbTiO3 films and the KTaO3 substrate. The domain width decreases as the film thickness is reduced following the square root dependence. This results in an increase of ferroelastic a/c domain walls and promotes the enhancement of the piezoresponse amplitude for the thinner PbTiO3 films. In addition, the piezoresponse amplitude of a 20 nm PbTiO3 film is comparable to that of a 40 nm PbTiO3 film, which indicates that the piezoelectric response of ferroelectric films may saturate at a certain film thickness and scarcely increase even after the film thickness reduces further. These results clarify the domain configurations of [101]-oriented PbTiO3 thin films and provide useful information for understanding the relationship between microstructures and piezoelectric properties in ferroelectric films.

Topological lattices such as vortices are of importance in both scientific research and application potential. Here, we observed periodic vortex-antivortex pairs in PbTiO3/SrTiO3 multilayered films deposited on orthorhombic (110)-oriented GdScO3 by pulsed laser deposition. Domain patterns of the PbTiO3 layers containing topological structures were analyzed in detail by using advanced transmission electron microscopy. It was found that by increasing the PbTiO3 thickness, a/c domains with extra c domains will form in the triangle a domains in pure flux-closure structures. Atomically resolved high-angle annular dark field-scanning TEM imaging demonstrates that this specific domain structure results in vortex-antivortex pairs at the junctions of extra c domains and the original flux-closure structure, forming a periodic vortex-antivortex array throughout the PbTiO3 layer. These results suggest a pathway for designing new topological structures in ferroelectric films.