材料科学
电容器
反铁电性
电介质
薄膜
铁电性
极化(电化学)
分析化学(期刊)
光电子学
电压
纳米技术
电气工程
化学
色谱法
物理化学
工程类
作者
Minh D. Nguyen,Yorick A. Birkhölzer,Evert Pieter Houwman,Gertjan Koster,Guus Rijnders
标识
DOI:10.1002/aenm.202200517
摘要
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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