Study of Correlation Effects in the High Formal Oxidation State Compound Sr$_2$CoO$_4$

TL;DR

This study investigates the electronic and magnetic properties of Sr$_2$CoO$_4$, focusing on correlation effects and hybridization, revealing complex behavior near critical U values and challenging simple spin state assignments.

Contribution

It provides a detailed analysis of correlation and hybridization effects in Sr$_2$CoO$_4$ using LDA+U and LDA, highlighting the complex magnetic states and the limitations of simple spin models.

Findings

Sr$_2$CoO$_4$ is ferromagnetic within LDA.

Critical U value of 2.5 eV causes a state transition.

Strong 3d-2p hybridization complicates spin state assignment.

Abstract

Two recent reports confirm that the newly synthesized Sr$_2$CoO$_4$ (formal oxidation state Co$^{4+}$) shows a high Curie temperature (~ 250 K), but they report different moments of 1.8 $\mu_B$ and 1 $\mu_B$ per Co. Using both commonly used functionals in the correlated band approach (LDA+U) as well as the local density approximation (LDA),the combined effects of correlation and hybridization with O 2p states are calculated and analyzed. Sr$_2$CoO$_2$ is already ferromagnetic within LDA (M=1.95 $\mu_B$). Increasing U from zero, the two LDA+U schemes affect the moment oppositely out to a critical value $U_c$=2.5 eV, at which point they transform discontinuously from different states to the same large U state. Fixing U at $U_c$, fixed spin moment calculations show similar behavior out to a minimum at 1$\mu_B$ (a half metallic state), beyond which the fully-localized-limit scheme jumps to a state with energy minimum very near 2$\mu_B$ very close to the LDA moment). Although the energy minima occur very near integer values of the moment/Co (1$\mu_B, 2$\mu_B$), the strong 3d-2p mixing and resulting 3d orbital occupations seem to preclude any meaningful S=1/2 or S=1 assignment to the Co ion.