First-principles calculations unveil electric-field and strain control of altermagnetic states in pentagonal FeO2, suggesting applications in low-power devices.
Two-dimensional multiferroics promise low-power, multifunctional devices, yet the intrinsic coexistence and mutual control of three coupled ferroic orders in a single layer remains elusive. Here, we identify pentagonal monolayer FeO₂ as an intrinsic triferroic altermagnet where ferroelectric (FE), ferroelastic (FA), and altermagnetic (AM) orders coexist and are tightly coupled, accompanied by a competing antiferroelectric (AFE) phase using first-principles calculations. The sole presence of glide mirror Mₓ symmetry in a FeO₂ sublayer, with the breaking of four-fold rotation C4z symmetry, induces in-plane vector ferroelectricity and twin-related ferroelastic strains. Both FE and AFE phases break combined parity - time symmetry and display sizable altermagnetic spin splitting with Néel temperatures over 200~K. Electric-field-induced rotation of the FE polarization reverses the sign of the spin splitting, while in-plane uniaxial strain triggers ferroelastic switching that simultaneously rotates the FE polarization vector by 90^∘ and reverses the AM state. These electric-field- and strain-mediated pathways interlink six distinct polarization states that can be selected purely by electric fields and/or mechanical strain. This work extends intrinsic triferroicity to pentagonal monolayers and outlines a symmetry-based route toward mechanically and electrically configurable altermagnetic spintronics.
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Guo et al. (2025) studied this question.
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