Correlation effects in CaCu3Ru4O12
arXiv:1211.2984 · doi:10.1103/PhysRevB.87.155122
Abstract
We have investigated the electronic structure of CaCu3Ru4O12 and LaCu3Ru4O12 using soft x-ray photoelectron and absorption spectroscopy together with band structure and cluster configuration interaction calculations. We found the Cu to be in a robust divalent ionic state while the Ru is more itinerant in character and stabilizes the metallic state. Substitution of Ca by La predominantly affects the Ru states. We observed strong correlation effects in the Cu 3d states affecting the valence band line shape considerably. Using resonant photoelectron spectroscopy at the Cu L3 edge we were able to unveil the position of the Zhang-Rice singlet states in the one-electron removal spectrum of the Cu with respect to the Ru-derived metallic bands in the vicinity of the chemical potential.
References in corpus (4)
Cited by in corpus (6)
- Competition between heavy-fermion and Kondo interaction in isoelectronic A-site ordered perovskites
- CaCuRuO: a high Kondo-temperature transition metal oxide
- Negative charge transfer energy in correlated compounds
- Strong Correlation Effects of A-site Ordered Perovskite CaCu3Ti4O12 revealed by Angle-Resolved Photoemission Spectroscopy
- Evidence for weak antilocalization-weak localization crossover and metal-insulator transition in CaCuRuO thin films
- Variation of strong correlation effects in A-site ordered perovskites CaCu3Ti4-xRuxO12: Photoemission and inverse photoemission studies