Local structural mechanism for enhanced energy storage properties in heterovalent doped NaNbO3 ceramics
In recent years, there is a growing interest for new lead-free oxides with reversible antiferroelectric (AFE)-ferroelectric (FE) phase transition for high-power energy-storage applications. NaNbO3-based ceramics are particularly attractive due to their easy synthesis and cost-effectiveness. In order...
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Published in | Journal of the European Ceramic Society Vol. 44; no. 3; pp. 1597 - 1609 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.03.2024
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Subjects | |
Online Access | Get full text |
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Summary: | In recent years, there is a growing interest for new lead-free oxides with reversible antiferroelectric (AFE)-ferroelectric (FE) phase transition for high-power energy-storage applications. NaNbO3-based ceramics are particularly attractive due to their easy synthesis and cost-effectiveness. In order to stabilize reversible AFE-FE phase transition, NaNbO3 is doped with a combination of heterovalent substitutions, although the underlying structural mechanism for the same is poorly understood. Here, we investigated local and average structures of Ca/Zr doped NaNbO3 using neutron total scattering. We show that Ca/Zr doping increases the average AFE phase (Pbma) fraction, however, the material remains as a composite of both FE (P21ma) and AFE regions. Analysis of local structure suggests that increase in the long-range AFE phase results from more extensive twinning of local FE regions, due to introduced charge disorder. We propose that enhanced energy-storage properties of Ca/Zr-doped NaNbO3 arises from localized twin boundary motion between the defect-induced pinning centers. |
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ISSN: | 0955-2219 |
DOI: | 10.1016/j.jeurceramsoc.2023.10.072 |