Density functional calculations for structural, electronic, and magnetic properties of gadolinium-oxide clusters

作者：Yuan, H K; Chen, H^*; Tian, C L; Kuang, A L; Wang, J Z

来源：Journal of Chemical Physics, 2014, 140(15): 154308.

DOI：10.1063/1.4871410

Gadolinium-oxide clusters in various sizes and stoichiometries have been systematically studied by employing the density functional theory with the generalized gradient approximation. The clusters in bulk stoichiometry are relatively more stable and their binding energies increase with the increasing size. Stoichiometric (Gd2O3)(n) clusters of n = 1-3 prefer cage-like structures, whereas the clusters of n = 4-30 prefer compact structures layered by wedge-like units and exhibit a rough feature toward the bulk-like arrangement with small disorders of atomic positions. The polyhedral-cages analogous to carbon-fullerenes are stable isomers yet not the minimum energy configurations. Their stabilities can be improved by embedding one oxygen atom or a suitable cage to form core-shell configurations. The mostly favored antiferromagnetic couplings between adjacent Gd atoms are nearly degenerated in energy with their ferromagnetic couplings, resulting in super-paramagnetic characters of gadolinium-oxide clusters. The Ruderman-Kittel-Kasuya-Yosida (RKKY)-type mechanism together with the superexchange-type mechanism plays cooperation role for the magnetic interactions in clusters. We present, as a function of n, calculated binding energies, ionization potential, electron affinity, and electronic dipole moment.

• 出版日期2014-4-21
• 单位西南大学