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Theoretical analysis reveals dominant altermagnetic instability in ruthenium dioxide at low temperatures, highlighting unique magnetic ordering mechanisms.
We study the instability in RuO2 using the Hartree–Fock approximation followed by the random phase approximation. We employ a three-orbital Hubbard model without spin-orbit coupling. An analysis of the eigenvalues and eigenvectors of the static susceptibility in the non-magnetic phase for various local interaction parameters U, JH, and hole doping n shows that the spin susceptibility is the dominant response channel. In the stoichiometric system without spin-orbit coupling, commensurate altermagnetic order is identified as the leading instability at sufficiently low temperatures, whereas at higher temperatures or finite hole doping, incommensurate wave vectors emerge. To elucidate the origin of the magnetic instability, we analyze the band splitting by the staggered Weiss field and discuss the qualitative difference between altermagnets and antiferromagnets.
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Csontosová et al. (2026) studied this question.
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