Superlattice-induced ferroelectricity in charge-ordered La${}_{1/3}$Sr${}_{2/3}$FeO${}_3$

Abstract

Charge-order-driven ferroelectrics are an emerging class of functional materials, distinct from conventional ferroelectrics, where electron-dominated switching can occur at high frequency. Despite their promise, only a few systems exhibiting this behavior have been experimentally realized thus far, motivating the need for new materials. Here, we use density functional theory to study the effect of artificial structuring on mixed-valence solid-solution La${}_{1/3}$Sr${}_{2/3}$FeO${}_3$ (LSFO), a system well-studied experimentally. Our calculations show that A-site cation (111)-layered LSFO exhibits a ferroelectric charge-ordered phase in which inversion symmetry is broken by changing the registry of the charge order with respect to the superlattice layering. The phase is energetically degenerate with a ground-state centrosymmetric phase, and the computed switching polarization is 39 $\mu$C/cm${}^2$, a significant value arising from electron transfer between Fe ions. Our calculations reveal that artificial structuring of LSFO and other mixed valence oxides with robust charge ordering in the solid solution phase can lead to charge-order-induced ferroelectricity.

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Cited by in corpus (3)

• Two-dimensional multiferroic metal with voltage-tunable magnetization and metallicity
• Electron-lattice coupling contributions to polarization switching in charge-order-induced ferroelectrics
• First-principle Study of Multiple Metastable Charge Ordering States in La${}_{1/3}$Sr${}_{2/3}$FeO${}_3$