de.mpg.escidoc.pubman.appbase.FacesBean
English
 
Help Guide Disclaimer Contact us Login
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Electronic properties of lanthanide oxides from the GW perspective

MPS-Authors
http://pubman.mpdl.mpg.de/cone/persons/resource/persons22010

Rinke,  Patrick
Theory, Fritz Haber Institute, Max Planck Society;

http://pubman.mpdl.mpg.de/cone/persons/resource/persons22064

Scheffler,  Matthias
Theory, Fritz Haber Institute, Max Planck Society;

Locator
There are no locators available
Fulltext (public)

e125115.pdf
(Publisher version), 2MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Jiang, H., Rinke, P., & Scheffler, M. (2012). Electronic properties of lanthanide oxides from the GW perspective. Physical Review B, 86(12): 125115. doi:10.1103/PhysRevB.86.125115.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0010-1665-3
Abstract
A first-principles understanding of the electronic properties of f -electron systems is currently regarded as a great challenge in condensed-matter physics because of the difficulty in treating both localized and itinerant states on the same footing by the current theoretical approaches, most notably density-functional theory (DFT) in the local-density or generalized gradient approximation (LDA/GGA). Lanthanide sesquioxides (Ln2O3) are typical f -electron systems for which the highly localized f states play an important role in determining their chemical and physical properties. In this paper, we present a systematic investigation of the performance of many-body perturbation theory in the GW approach for the electronic structure of the whole Ln2O3 series. To overcome the major failure of LDA/GGA, the traditional starting point for GW, for f -electron systems, we base our GW calculations on Hubbard U corrected LDA calculations (LDA+U). The influence of the crystal structure, the magnetic ordering, and the existence of metastable states on the electronic band structures are studied at both the LDA+U and the GW level. The evolution of the band structure with increasing number of f electrons is shown to be the origin for the characteristic structure of the band gap across the lanthanide sesquioxide series. A comparison is then made to dynamical mean-field theory (DMFT) combined with LDA or hybrid functionals to elucidate the pros and cons of these different approaches.