Holes' character and bond versus charge disproportionation in $s-p$ $ABX_{3}$ perovskites

Abstract

We use density functional theory methods to study the electronic structures of a series of $s-p$ cubic perovskites $ABX_{3}$: the experimentally available SrBiO$_{3}$, BaBiO$_{3}$, BaSbO$_3$, CsTlF$_{3}$, and CsTlCl$_{3}$, as well as the hypothetical MgPO$_{3}$, CaAsO$_{3}$, SrSbO$_{3}$, and RaMcO$_3$. We use tight-binding modeling to calculate the interatomic hopping integrals $t_{spσ}$ between the $B-s$ and $X-p$ atomic orbitals and charge-transfer energies $Δ$, which are the two most important parameters that determine the low-energy electron and hole states of these systems. Our calculations elucidate several trends in $t_{spσ}$ and $Δ$ as one moves across the periodic table, such as the relativistic energy lowering of the $B-s$ orbital in heavy $B$ cations leading to strongly negative $Δ$ values. Our results are discussed in connection with the general phase diagram for $s - p$ cubic perovskites proposed in Ref. 26, where the parent superconductors SrBiO$_{3}$ and BaBiO$_{3}$ are found to be in the regime of negative $Δ$ and large $t_{spσ}$. Here, we explore this further and search for new materials with similar parameters, which could lead to the discovery of new superconductors. Also, some considerations are offered regarding a possible relation between the physical properties of a given $s - p$ compound (such as its tendency to bond disproportionate and the maximal achievable superconducting transition temperature) and its electronic structure.