Flipping of electronic spins in BiFeO3 via chiral d-d excitations

Abstract

BiFeO3 is a multiferroic material featuring ferroelectricity and noncollinear antiferromagnetism. Definitive and efficient control of the characteristic spin texture of BiFeO3 is attractive for emerging quantum devices. In this regard, crystal-field d→ d excitations localized on Fe atomic sites in BiFeO3 provide an avenue for manipulation of the spin texture as they induce a complex interplay among the spin, charge, and lattice degrees of freedom. In this work, the ab initio GW-BSE method is used to characterize these excitations within an excitonic picture. We find that the d-d transitions appear as strongly bound, chiral, spin-flip excitons deep within the electronic band gap as a result of the intricate competition between the lattice potential, the antiferromagnetic ordering, the spin-orbit coupling, and the electron-hole interaction. Most crucially, these excitons are composed of electron-hole pairs with opposite spins that constitute almost all of their total angular momentum. These excitons of specific angular momentum can be selectively excited using circularly polarized light, consequently modulating the local magnetic moment.

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