Electronic structure and magnetic properties of $\mathrm{CaCr}\mathrm{O}_3$: The interplay between spin- and orbital-orderings

Abstract

The electronic structure and magnetic properties of CaCr$\mathrm{O}_3$ have been calculated by two methods, including hybrid-exchange density-function theory and density-functional theory + $U$. The computed densities of states from both of these methods are in a qualitative agreement with the previous x-ray spectroscopy. On the other hand, the opening of the band gap separates them apart. hybrid-exchange density-functional theory always gives a finite band gap, down to $\sim 1.2$ eV from HSE06 functional, whereas by tuning the Hubbard-$U$ parameter down to $0.5$ eV, a conducting state with AFM-C (defined in the text) spin configuration can be achieved. From hybrid density-functional theory, the computed nearest-neighbouring exchange interaction along the $c$-axis and in the $ab$-plane are $\sim 4$ meV and $\sim 6$ meV (anti-ferromagnetic), respectively, which are qualitatively in agreement with the previous magnetic measurements. These anti-ferromagnetic exchange interaction, together with the in-plane anti-ferro-orbital ordering will induce a spin-orbital frustration, which could play a role for the abnormal electronic properties in CaCrO$_3$. In hybrid-exchange density-functional theory, an abrupt reduction ($\sim 0.2$ eV) of the majority-spin band gap of the ferromagnetic state between 60 K and 100 K has been found as lowering temperature, which shows a strong link to the previous optical conductivity measurements in [A. C. Komarek, et. al., Phys. Rev. B \textbf{84}, 125114 (2011)]. In sharp contrast, the density-functional theory + $U$ methods predicted AFM-C state as the lowest AFM state for the crystal structure measured below 90 K, above which AFM-A is however the lowest. The closely related concepts including electron-hole liquid and surface-plasmon-mediating spin-spin interactions have been discussed as well.