Enhanced anodic catalytic performance in PrFeO of perovskite materials via Co-doping with Sr and VB subgroup metals (V, Nb, Ta)

The anodic catalytic capability of PrFeO is restricted by the Fe-site element type in the perovskite material structure due to its low electrical conductivity of electrons. Here, we present a strategy for tuning the Fe-site element type via Sr and VB subgroup metals (V, Nb, Ta) co-doping to enhance the anodic catalytic performance of PrFeO anode materials. Our calculations show that Sr and Nb co-doping has suitable hydrogen adsorption energy for PrFeO anode materials, and its adsorption energy is adjusted to −0.717 eV, which is more suitable to absorb the hydrogen molecule than other high-profile perovskite anode materials. Meanwhile, after the doped surface is adsorbed by hydrogen molecules, the bond length lengthens until it breaks, and one of the broken hydrogen atoms moves directly above the surface oxygen atom, which is beneficial for accelerating the anodic catalytic reaction. Thus, the PrSrFeNbO material is a promising perovskite anode catalyst. Interestingly, the stability of PrFeO is significantly affected by the oxygen vacancy content; the structural stability of the undoped system can be maintained via Sr and Nb co-doping to avoid decomposition, which provides new thinking to maintain the high stability of perovskite ferrite materials. Furthermore, we find that relative to the PrFeO, the PrSrFeNbO surface of hydrogen adsorption has obvious charge transfer and upward shift of the d-band center. Our anodic catalytic theoretical work shows that Sr and Nb co-doping can effectively enhance the catalytic performance of the PrFeO ferrite materials.