ABSTRACT
We have investigated the structural, bonding, and electronic properties of both ferroelectric (FE) and paraelectric (PE) phases of the hexagonal LuMnO3 compound using calculations based on density functional theory. The structural properties have been determined by employing the generalized gradient approximation with Perdew-Burke-Ernzerhof and Wu-Cohen parameterization. The bonding and electronic properties have been treated by recently developed modified Becke-Johnson exchange potential, which succeeded to open a band gap for both PE and FE phases, in agreement with experimental predictions. The Bader's topological analysis of electronic density showed that the character of the Lu-O axial bonds changes when the crystal exhibits the PE â FE structural transition. This fact is in agreement with experimental findings. The covalent character of the Lu-O bond significantly increases due to orbital hybridization between the Lu 5dz(2) and O 2pz-states. This bonding mechanism causes the ferroelectricity in the hexagonal LuMnO3 compound.
ABSTRACT
Structural, electronic and optical properties of the antisite BiMO4 defect in Bi12MO20 sillenites (BMO, M=Si, Ge, Ti) were investigated using density functional theory. The defect is studied in neutral, positively and negatively charged states. It is demonstrated that within the neutral defect the Bi 6s(2) lone pair is broken and the valence state of the Bi is 4+ (6s(1)). Within the charged defects, the Bi 6s orbital is found to be either full (Bi(3+): 6s(2)) or empty (Bi(5+): 6s(0)). All three charged states introduce energy bands within the BMO gap. By analyzing possible transitions between them we deduced a simple model of functioning of the BiMO4 defect that is able to explain the photochromic and photorefractive effect in sillenites and that reproduces almost all known experimental facts.
