Spin-dependent interactions in orbital-density-dependent functionals: Noncollinear Koopmans spectral functionals

The presence of spin-orbit coupling or noncollinear magnetic spin states can have dramatic effects on the ground-state and spectral properties of materials, in particular on the band structure. Here, we develop noncollinear Koopmans-compliant functionals based on Wannier functions and density-functional perturbation theory, targeting accurate spectral properties in the quasiparticle approximation. Our noncollinear Koopmans-compliant theory involves functionals of four-component orbital densities that can be obtained from the charge and spin-vector densities of Wannier functions. We validate our approach on four emblematic nonmagnetic and magnetic semiconductors where the effect of spin-orbit coupling goes from small to very large: the III-IV semiconductor GaAs, the transition-metal dichalcogenide WSe2, the cubic perovskite CsPbBr3, and the ferromagnetic semiconductor CrI3. The predicted band gaps are comparable in accuracy to state-of-the-art many-body perturbation theory and include spin-dependent interactions and screening effects that are missing in standard diagrammatic approaches based on the random phase approximation. While the inclusion of orbital- and spin-dependent interactions in many-body perturbation theory requires self-screening or vertex corrections, they emerge naturally in the Koopmans-functionals framework.