Origin of OER catalytic activity difference of oxygen-deficient perovskites AMnO (A = Ca, Sr): A theoretical study.

Mn-based oxygen-deficient perovskite catalysts AMnO (A = Ca, Sr) have been experimentally proved high oxygen evolution reaction (OER) activities for replacing Pt in oxygen electrocatalysis. Nevertheless, the correlation between the fundamental electronic structure at room temperature and the corresponding electrocatalysis is not fully accessible. In this paper, we combine the ground state density functional theory (DFT) method and dynamic mean-field theory (DFT+DMFT) at room temperature to investigate the origin of the OER difference for electrocatalysts AMnO (A = Ca, Sr). We find that at room temperature the highest occupied Mn d orbital in the square pyramidal crystal field of oxygen-deficient perovskites AMnO with insulating properties can provide a moderate bonding strength with intermediate hydroxyl OH*, leading to a high OER catalytic activity. According to the electronic structure analysis, we observe that replacing the A-site element Ca by Sr with the larger ionic radii would result in a higher OER activity due to the weakened hybridization between the Mn d orbital and the O p orbital of OH*. This insight could provide hints for the screening metal oxide electrocatalysts in the applications of the energy storage and conversion.