Using density functional calculations, we find that the newly synthesized Ca2FeOsO6 has the high-spin Fe3+ (3d5)-Os5+ (5d3) state. The octahedral Os5+ ion has a large intrinsic exchange splitting, and its t2g↑3 configuration makes the spin-orbit coupling ineffective. Moreover, there is a strong antiferromagnetic (AF) coupling between the neighboring Fe3+ (S = 5/2) and Os5+ (S = -3/2), but the AF couplings within both the fcc Fe3+ and Os5+ sublattices are one order of magnitude weaker. Therefore, a magnetic frustration is suppressed and a stable ferrimagnetic (FiM) ground state appears. This FiM order is due to the virtual hopping of the t2g electrons from Os5+ (t2g↓3) to Fe3+ (t2g↑3eg↑2). However, if the experimental bended Fe3+-O2−-Os5+ exchange path gets straight, the eg hopping from Fe3+ (t2g↑3eg↑2) to Os5+ (t2g↑3) would be facilitated and then a ferromagnetic (FM) coupling would occur.
@article{arxiv.1406.3101,
title = {Ferrimagnetism in the double perovskite Ca2FeOsO6: a density functional study},
author = {Hongbo Wang and Shasha Zhu and Xuedong Ou and Hua Wu},
journal= {arXiv preprint arXiv:1406.3101},
year = {2014}
}