| Home > Publications database > First-Principles Calculation of Electronic Excitations in Solids with SPEX |
| Journal Article | PreJuSER-10562 |
; ; ;
2010
Oldenbourg
München
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Please use a persistent id in citations: http://hdl.handle.net/2128/18346 doi:10.1524/zpch.2010.6110
Abstract: We describe the software package SPEX, which allows first-principles calculations of quasiparticle and collective electronic excitations in solids using techniques from many-body perturbation theory. The implementation is based on the full-potential linearized augmented-plane-wave (FLAPW) method, which treats core and valence electrons on an equal footing and can be applied to a wide range of materials, including transition metals and rare earths. After a discussion of essential features that contribute to the high numerical efficiency of the code, we present illustrative results for quasiparticle band structures calculated within the GW approximation or the electronic self-energy, electron-energy-loss spectra with inter- and intraband transitions as well as local-field effects, and spin-wave spectra of itinerant ferromagnets. In all cases the inclusion of many-body correlation terms leads to very good quantitative agreement with experimental spectroscopies.
Keyword(s): J ; Many-Body Perturbation Theory (auto) ; Self-Energy (auto) ; Quasiparticle Band Structure (auto) ; Dielectric Function (auto) ; Spin Waves (auto)
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