Tunable and Persistent Macroscopic Polarization in Nominally Centrosymmetric Defective Oxides

TL;DR

This study demonstrates that defect-induced symmetry breaking in centrosymmetric oxides can produce persistent, switchable polarization, opening new avenues for environmentally friendly polar materials in energy and electronics.

Contribution

It introduces a defect-mediated method to induce and control polarization in centrosymmetric oxides, which was previously unachieved.

Findings

Persistent pyroelectric effects with high coefficients.

Switchable polarization governed by oxygen vacancy redistribution.

Potential for high-performance, sustainable polar materials.

Abstract

Introducing symmetry breaking in materials enables the emergence of functionalities. This can be microscopically and macroscopically driven by applying external stimuli such as mechanical stress, electric field, temperature, and chemical modification. For instance, non-zero net dipole moments are formed in a material with the presence of local charged defects or their clusters, which can alter the crystal structure, charge states, and electrostatic potential across the material. Here, we demonstrate a conceptual approach to defects-mediated symmetry breaking that allows for built-in polarization in a centrosymmetric oxide, $\mathrm{Gd}_x\mathrm{Ce}_{1-x}\mathrm{O}_{2-\delta}$ (CGO) films, via creating a macroscopic charge asymmetry. Our results show that switchable and enduring polarization in CGO films is governed by the redistribution of oxygen vacancies. This leads to notable and persistent pyroelectric effects with coefficient of approximately 180 $\mu\mathrm{C}\cdot\mathrm{m}^{-2}\cdot\mathrm{K}^{-1}$. Our findings highlight the potential to develop high-performance, sustainable, environmentally friendly polar film materials by manipulating ionic defects from their centrosymmetric ground states. This approach provides new opportunities to expand polar materials in current and future energy and electronic applications.