Improper antiferroelectricity in NaNbO3-based perovskites driven by antiferrodistortive modulation

Chao Xu, Nengneng Luo (), Cenchen Zhong, Gengguang Luo, Ruoxuan Che, Xuyun Guo, Changsheng Chen, Shujun Zhang () and Ye Zhu ()
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Chao Xu: The Hong Kong Polytechnic University
Nengneng Luo: Guangxi University
Cenchen Zhong: The Hong Kong Polytechnic University
Gengguang Luo: Guangxi University
Ruoxuan Che: Guangxi University
Xuyun Guo: The Hong Kong Polytechnic University
Changsheng Chen: The Hong Kong Polytechnic University
Shujun Zhang: University of Wollongong
Ye Zhu: The Hong Kong Polytechnic University

Nature Communications, 2025, vol. 16, issue 1, 1-10

Abstract: Abstract Perovskite materials exhibit a wide array of fascinating properties arising from various structural instabilities and the interplay between them. Probing such instabilities demands the use of high-resolution, high-sensitivity characterization techniques to prototypical materials with minimized complexity. Here we present the discovery of unconventional improper antiferroelectricity driven by antiferrodistortive modulation in NaNbO3-based perovskites, using advanced scanning transmission electron microscopy conducted on compositionally engineered samples, with a focus on Mn-doped (Na0.65Ag0.20Ca0.15)(Nb0.85Ti0.15)O3. Contrary to the prevailing understanding that such octahedral-rotation-driven improper polarization requires symmetry breaking at the interfaces in layered perovskites, our observation indicates that it can also be enabled in non-layered perovskites, by modulated octahedral rotations following an alternating sequence of (a−b−c+)m (m = integer) and a−b+c+ that is tunable via chemical doping. Combining with first-principles calculations and group theoretical analysis, we reveal a multimode interaction picture to generate the unique dipole order, resolving its long-standing structural ambiguity. The identified mechanism for octahedral-rotation-driven improper polarization represents a new design freedom to tailor the interplay of instabilities for coupled functionalities in perovskite oxides.

Date: 2025
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DOI: 10.1038/s41467-025-60568-w

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