Tailoring high-energy storage NaNbO3-based materials from antiferroelectric to relaxor states

Journal Article (2023)
Author(s)

Mao Hua Zhang (Technische Universität Darmstadt)

Hui Ding (Technische Universität Darmstadt)

Sonja Egert (Technische Universität Darmstadt)

Changhao Zhao (Technische Universität Darmstadt)

Lorenzo Villa (Technische Universität Darmstadt)

Lovro Fulanović (Technische Universität Darmstadt)

Pedro B. Groszewicz (TU Delft - Applied Sciences)

Gerd Buntkowsky (Technische Universität Darmstadt)

Hans Joachim Kleebe (Technische Universität Darmstadt)

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Research Group
RST/Storage of Electrochemical Energy
DOI related publication
https://doi.org/10.1038/s41467-023-37060-4 Final published version
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Publication Year
2023
Language
English
Research Group
RST/Storage of Electrochemical Energy
Issue number
1
Volume number
14
Article number
1525
Downloads counter
207
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Abstract

Reversible field-induced phase transitions define antiferroelectric perovskite oxides and lay the foundation for high-energy storage density materials, required for future green technologies. However, promising new antiferroelectrics are hampered by transition´s irreversibility and low electrical resistivity. Here, we demonstrate an approach to overcome these problems by adjusting the local structure and defect chemistry, delivering NaNbO3-based antiferroelectrics with well-defined double polarization loops. The attending reversible phase transition and structural changes at different length scales are probed by in situ high-energy X-ray diffraction, total scattering, transmission electron microcopy, and nuclear magnetic resonance spectroscopy. We show that the energy-storage density of the antiferroelectric compositions can be increased by an order of magnitude, while increasing the chemical disorder transforms the material to a relaxor state with a high energy efficiency of 90%. The results provide guidelines for efficient design of (anti-)ferroelectrics and open the way for the development of new material systems for a sustainable future.