Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT

Freigegeben

Zeitschriftenartikel

Importance of tetrahedral coordination for high-valent transition-metal oxides: YCrO4 as a model system

MPG-Autoren
/persons/resource/persons126888

Tsirlin,  A. A.
Chemical Metal Science, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

/persons/resource/persons134454

Rabie,  M. G.
Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

/persons/resource/persons126592

Efimenko,  A.
Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

/persons/resource/persons126666

Hu,  Z.
Zhiwei Hu, Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

/persons/resource/persons126881

Tjeng,  L. H.
Liu Hao Tjeng, Physics of Correlated Matter, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

Externe Ressourcen
Es sind keine externen Ressourcen hinterlegt
Volltexte (beschränkter Zugriff)
Für Ihren IP-Bereich sind aktuell keine Volltexte freigegeben.
Volltexte (frei zugänglich)
Es sind keine frei zugänglichen Volltexte in PuRe verfügbar
Ergänzendes Material (frei zugänglich)
Es sind keine frei zugänglichen Ergänzenden Materialien verfügbar
Zitation

Tsirlin, A. A., Rabie, M. G., Efimenko, A., Hu, Z., Saez-Puche, R., & Tjeng, L. H. (2014). Importance of tetrahedral coordination for high-valent transition-metal oxides: YCrO4 as a model system. Physical Review B, 90(8): 085106, pp. 1-6. doi:10.1103/PhysRevB.90.085106.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0023-CF4B-F
Zusammenfassung
We have investigated the electronic structure of the high oxidation state material YCrO 4 within the framework of the Zaanen-Sawatzky-Allen phase diagram. While Cr 4+-based compounds such as SrCrO 3/CaCrO 3 and CrO 2 can be classified as small-gap or metallic negative-charge-transfer systems, we find using photoelectron spectroscopy that YCrO 4 is a robust insulator despite the fact that its Cr ions have an even higher formal valence state of 5+. We reveal using band-structure calculations that the tetrahedral coordination of the Cr 5+ ions in YCrO 4 plays a decisive role, namely to diminish the bonding of the Cr 3d states with the top of the O 2p valence band. This finding not only explains why the charge-transfer energy remains effectively positive and the material stable, but also opens up a new route to create doped carriers with symmetries different from those of other transition-metal ions.