We investigate the metal-insulator transition in the layered Ruddelsden
Popper series of strontium iridates Srn+1IrnO3n+1. Tight-binding models of t2g
orbitals for n = 1, 2, and infinity are constructed, and changes in band
dispersion due to dimensionality and spin-orbit coupling are presented.
Identifying the states near the Fermi level to be predominantly Jeff = 1/2, we
use an effective Hubbard model to study the effect of correlations. Transitions
from a metallic state to various magnetically ordered states at different
critical interactions are obtained. A canted antiferromagnetic insulator is
found for Sr2IrO4, a c-axis collinear antiferromagnetic insulator for Sr3Ir2O7,
and non-coplanar canted antiferromagnetic insulator via magnetic metal for
SrIrO3. We derive the strong-coupling spin-model and compare the magnetic
ordering patterns obtained in the weak and strong coupling limits. We find that
they are identical, indicating that magnetic ordering is not sufficient to
justify Mott physics in this series of iridates.Comment: 11 pages, 18 figure