Ferromagnetic Ferroelectricity due to Orbital Ordering

Abstract

Realization of ferromagnetic ferroelectricity, combining two ferroic orders in a single phase, is the longstanding problem of great practical importance. One of the difficulties is that ferromagnetism alone cannot break inversion symmetry $\mathcal{I}$. Therefore, such a phase cannon be obtained by purely magnetic means. Here, we show how it can be designed by making orbital degrees of freedom active. The idea can be traced back to a basic principle of interatomic exchange, which states that an alternation of occupied orbitals along a bond (i.e., antiferro orbital order) favors ferromagnetic coupling. Moreover, the antiferro orbital order breaks $\mathcal{I}$, so that the bond becomes not simply ferromagnetic but also ferroelectric. Then, we formulate main principles governing the realization of such a state in solids, namely: (i) The magnetic atoms should not be located in inversion centers, as in the honeycomb lattice; (ii) The orbitals should be flexible enough to adjust they shape and minimize the energy of exchange interactions; (iii) This flexibility can be achieved by intraatomic interactions, which are responsible for Hund's second rule and compete with the crystal field splitting; (iv) For octahedrally coordinated transition-metal compounds, the most promising candidates appear to be iodides with a $d^2$ configuration and relatively weak $d$-$p$ hybridization. Such a situation is realized in the van der Walls compound VI${}_3$, which we expect to be ferromagnetic ferroelectric.

22 pages, 11 figures

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