arXiv subjects

Mao-Hua Zhang

Publications and source records attributed to Mao-Hua Zhang.

4 recordsLinked to original sources

arXiv2026

A Geometric Pathway for Tuning Ferroelectric Properties via Polar State Reconfiguration

We report the discovery of a geometric pathway for tuning ferroelectric properties through thermally driven reconfiguration between coexisting polar states in Li-substituted NaNbO3. Using first-principles density functional theory calculation and 7Li solid-state nuclear magnetic resonance spectroscopy measurement, we reveal that Li substitution creates two distinct polar configurations whose transformation under annealing enhances the Curie temperature and induces piezoelectric hardening. Our findings establish a geometrically-driven polar state reconfiguration mechanism, providing a general design principle for ferroics whereby macroscopic functional properties can be engineered via lattice geometry.

cond-mat.mtrl-sci↗

arXiv2026

Chemical heterogeneity at conducting ferroelectric domain walls

Natural interfaces in ferroic oxides have developed into versatile playgrounds for studying electronic correlation effects in 2D systems. The microscopic origin of the emergent local electronic properties is often debated, however, as quantitative atomic-scale characterization remains challenging. A prime example is enhanced conductivity at ferroelectric domain walls, attributed to mechanisms ranging from local band gap reduction to point defect accumulations. Here, we resolve the microscopic mechanisms for domain wall conduction in the ferroelectric model system BiFeO3, by combining transport measurements with atom probe tomography to quantify the local chemical composition and correlate it with the electrical properties. Significant chemical variations along the walls are observed, demonstrating an outstanding chemical flexibility at domain walls, which manifest in spatially varying physical properties. The results give a unifying explanation for the diverse electronic behavior observed and establish the fundamental notion that multiple conduction mechanisms can coexist within individual domain walls.

cond-mat.mtrl-sci↗

arXiv2024

Origin of Increased Curie Temperature in Lithium-Substituted Ferroelectric Niobate Perovskite: Enhancement of the Soft Polar Mode

The functionality of ferroelectrics is often constrained by their Curie temperature, above which depolarization occurs. Lithium (Li) is the only experimentally known substitute that can increase the Curie temperature in ferroelectric niobate-based perovskites, yet the mechanism remains unresolved. Here, the unique phenomenon in Li-substituted KNbO3 is investigated using first-principles density functional theory. Theoretical calculations show that Li substitution at the A-site of perovskite introduces compressive chemical pressure, reducing Nb-O hybridization and associated ferroelectric instability. However, the large off-center displacement of the Li cation compensates for this reduction and further enhances the soft polar mode, thereby raising the Curie temperature. In addition, the stability of the tetragonal phase over the orthorhombic phase is predicted upon Li substitution, which reasonably explains the experimental observation of a decreased orthorhombic-to-tetragonal phase transition temperature. Finally, a metastable anti-phase polar state in which the Li cation displaces oppositely to the Nb cation is revealed, which could also contribute to the variation of phase transition temperatures. These findings provide critical insights into the atomic-scale mechanisms governing Curie temperature enhancement in ferroelectrics and pave the way for designing advanced ferroelectric materials with improved thermal stability and functional performance.

cond-mat.mtrl-sci↗

arXiv2024

Heterogeneous antiferroelectric ordering in NaNbO3-SrSnO3 ceramics revealed by direct superstructure imaging

NaNbO3-based antiferroelectric materials offer a promising pathway towards greener and more cost-effective energy storage devices. However, their intrinsic structural instabilities often lead to reduced energy density that compromises their performance and longevity. In this brief communication, we demonstrate how Dark-Field X-ray Microscopy, when carried out on the characteristically weak 1/4{843}pc superstructure reflection, can map the antiferroelectric phase and its strain heterogeneity in typically small, deeply-embedded grains of a NaNbO3 and 0.95NaNbO3-0.05SrSnO3 ceramics, representative of different phase transition behavior. Our results clearly evidences the stabilizing effect of SrSnO3 on the antiferroelectric phase by enhancing the degree of mesostructural order. In doing so, our method establishes a new platform for exploring the impact of disorder on the long-range strain heterogeneity within antiferroelectrics and other materials with modulated crystal structures.

cond-mat.mtrl-sci↗