Switchable Polarization in an A-Site Deficient Perovskite through Vacancy and Cation Engineering

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Authors: Suguru Yoshida, Olivier Hernandez, Jinsuke Miyake, Kei Nakayama, Ryo Ishikawa, Hajime Hojo, Yuichi Ikuhara, Venkatraman Gopalan, Katsuhisa Tanaka, Koji Fujita
Cited by: 3
References: 75

Abstract

While defects are unavoidable in crystals and often detrimental to material performance, they can be a key ingredient for inducing functionalities when tailored. Here, we show that an A-site-deficient perovskite Y 1/3 TaO 3 exhibits switching-like polarization response at room temperature in the Pb 2 1 m phase, enabled by ordered vacancies coupled with TaO 6 octahedral rotations. Defect-ordered perovskites are frequently trapped in centrosymmetric incommensurate states due to competing structural instabilities; we circumvent this by favoring rotational over off-centering instability through compositional selection. Unlike canonical improper ferroelectrics that are ferrielectric, the vanishing dipoles on vacancy layers in Y 1/3 TaO 3 allow for a net ferroelectric alignment of local dipoles, resulting in enhanced polarization. Upon heating, Y 1/3 TaO 3 transforms to a paraelectric incommensurate phase at ≃750 K, whose atomic arrangement mirrors the domain topology observed in hybrid improper ferroelectrics. Superspace analysis of the modulated phase reveals a route to improve room-temperature polarization, achieved through epitaxial strain, as confirmed by our lattice-dynamics calculations. This defect-ordering strategy should be generalizable to other improper ferroelectrics, including magnetoelectric multiferroics, providing a pathway to amplify otherwise limited macroscopic polarization.

Fields of Study & Subjects

Multiferroics and related materials Ferroelectric and Piezoelectric Materials Ferroelectric and Negative Capacitance Devices

Publication details

Journal / source
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Volume
148
Issue
4
Pages
4557–4567
Publication date
23 January 2026
Language
EN