Publication | Open Access
Enhancing the Energy‐Storage Density and Breakdown Strength in PbZrO<sub>3</sub>/Pb<sub>0.9</sub>La<sub>0.1</sub>Zr<sub>0.52</sub>Ti<sub>0.48</sub>O<sub>3</sub>‐Derived Antiferroelectric/Relaxor‐Ferroelectric Multilayers
70
Citations
46
References
2022
Year
DielectricsEngineeringBreakdown StrengthMultiferroicsFerroelectric ApplicationMultilayer Period NumberQuantum MaterialsAntiferroelectric/relaxor‐ferroelectric MultilayersMaterials ScienceEnergy StorageDomain StructureElectrical PropertyMultilayer Thin‐film CapacitorsMaterial AnalysisApplied PhysicsFerroelectric MaterialsThin FilmsFunctional MaterialsEnergy‐storage Density
Abstract Multilayer thin‐film dielectric capacitors with high energy‐storage performance and fast charge/discharge speed have significantly affected the development of miniaturized pulsed‐power devices. Here, the interfacial strain in epitaxial multilayers of antiferroelectric PbZrO 3 and relaxor‐ferroelectric Pb 0.9 La 0.1 Zr 0.52 Ti 0.48 O 3 is shown to significantly enhance the maximum polarization of the multilayer thin‐film capacitors, beyond that of the composing individual layers. Insights obtained from atomically resolved energy‐dispersive X‐ray spectroscopy and high‐resolution X‐ray diffraction analysis of the interface and domain structure are used to develop phenomenological models that explain the observed trends in breakdown strength and energy‐storage density as a function of multilayer period number. The underlying mechanism is the mechanical coupling between the layers that depends on the individual layer thicknesses. These factors result in a strongly enhanced recoverable energy‐storage density (increased by a factor of 4 to ≈128.4 J cm −3 ) with high efficiency (≈81.2%). Moreover, the multilayer films show almost fatigue‐free energy‐storage performance after 10 10 switching cycles, even at elevated temperatures up to 220 °C, demonstrating their robustness. The outstanding properties show the great potential of epitaxial multilayers for energy‐storage applications, due to the well‐defined separate layers and coupling of properties across the interfaces, not present in ceramic composites.
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