Role of Local Structural Distortions on the Origin of <i>j</i> = 1/2 Pseudo-Spin State in Sodium Iridate

Na₂IrO₃ (NIO) is known to be a spin–orbit (SO) driven <i>j</i> = 1/2 pseudo-spin Mott–Hubbard (M–H) insulator. The mixing of <i>j</i> = 1/2 pseudo-spin derived from t_2g orbitals with the e_g orbitals has not been probed yet from the viewpoint of local structural distortions. Using a combination of theoretical calculations and X-ray spectroscopy, we show that the energetics in the vicinity of Fermi level (<i>E</i>_F) is governed by SO interactions, electron correlation, and local octahedral distortions. The <i>j</i> = 3/2 and 1/2 pseudo-spin states have an admixture of both t_2g and e_g characters due to a local structural distortion. Reduction of the local octahedral symmetry also enables Ir 5d–O 2p hybridization around the <i>E</i>_F resulting in an M–H insulator with enhanced charge-transfer character. The possibility of the Slater insulator phase is also ruled out by a combination of the absence of room-temperature density of states in valence band spectra, calculated moments, and temperature-dependent magnetization measurements.