TY - JOUR
T1 - Tailoring high-energy storage NaNbO3-based materials from antiferroelectric to relaxor states
AU - Zhang, Mao Hua
AU - Ding, Hui
AU - Egert, Sonja
AU - Zhao, Changhao
AU - Villa, Lorenzo
AU - Fulanović, Lovro
AU - Groszewicz, Pedro B.
AU - Buntkowsky, Gerd
AU - Kleebe, Hans Joachim
AU - More Authors, null
PY - 2023
Y1 - 2023
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85150666076&partnerID=8YFLogxK
U2 - 10.1038/s41467-023-37060-4
DO - 10.1038/s41467-023-37060-4
M3 - Article
C2 - 36934123
AN - SCOPUS:85150666076
SN - 2041-1723
VL - 14
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1525
ER -