| 1. |
- Delczeg, Lorand, et al.
(författare)
-
Assessing common density functional approximations for the ab initio description of monovacancies in metals
- 2009
-
Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 80:20
-
Tidskriftsartikel (refereegranskat)abstract
- Using the exact muffin-tin orbitals method, we investigate the accuracy of five common density functional approximations for the theoretical description of the formation energy of monovacancies in three close-packed metals. Besides the local density approximation (LDA), we consider two generalized gradient approximation developed by Perdew and co-workers (PBE and PBEsol) and two gradient-level functionals obtained within the subsystem functional approach (AM05 and LAG). As test cases, we select aluminum, nickel, and copper, all of them adopting the face centered cubic crystallographic structure. Our results show that, compared to the recommended experimental values, LDA is be the most reliable approximation for the vacancy formation energies in these metals. However, taking into account also the performances of the functionals for the equation of state changes the final verdict in favor of the generalized gradient approximations.
|
|
| 2. |
- Delczeg-Czirjak, Erna Krisztina, 1978-, et al.
(författare)
-
Ab initio study of the elastic anomalies in Pd-Ag alloys
- 2009
-
Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 79
-
Tidskriftsartikel (refereegranskat)abstract
- Ab initio total-energy calculations, based on the exact muffin-tin orbital method, are used to determine the elastic properties of Pd1-xAgx random alloys in the face-centered-cubic crystallographic phase. The compositional disorder is treated within the coherent-potential approximation. The single crystal and polycrystalline elastic constants and the Debye temperature are calculated for the whole range of concentration, 0 <= x <= 1. It is shown that the variation in the elastic parameters of Pd-Ag alloys with chemical composition strongly deviates from a simple linear or parabolic trend. The complex electronic origin of these anomalies is demonstrated.
|
|
