Parametrization of LSDA+ for noncollinear magnetic configurations: Multipolar magnetism in UO
arXiv:1811.06864 · doi:10.1103/PhysRevMaterials.3.083802
Abstract
To explore the formation of noncollinear magnetic configurations in materials with strongly correlated electrons, we derive a noncollinear LSDA+ model involving only one parameter , as opposed to the difference between the Hubbard and Stoner parameters . Computing in the constrained random phase approximation, we investigate noncollinear magnetism of uranium dioxide UO and find that the spin-orbit coupling (SOC) stabilizes the 3 ordered magnetic ground state. The estimated SOC strength in UO is as large as 0.73 eV per uranium atom, making spin and orbital degrees of freedom virtually inseparable. Using a multipolar pseudospin Hamiltonian, we show how octupolar and dipole-dipole exchange coupling help establish the 3 magnetic ground state with canted ordering of uranium -orbitals. The cooperative Jahn-Teller effect does not appear to play a significant part in stabilizing the noncollinear 3 state, which has the lowest energy even in an undistorted lattice. The choice of parameter in the LSDA+ model has a notable quantitative effect on the predicted properties of UO, in particular on the magnetic exchange interaction and, perhaps trivially, on the band gap: The value of eV computed fully delivers the band gap of 2.11~eV in good agreement with experiment, and a balanced account of other pertinent energy scales.
arXiv comment14 pages, 9 figures
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