Tuned d-band states over lanthanum doped nickel oxide for efficient oxygen evolution reaction

Abstract

The d-band state of materials is an important descriptor for activity of oxygen evolution reaction (OER). For NiO materials, there is rarely concern about tuning their d-band states to tailor the OER behaviors. Herein, NiO nanocrystals with doping small amount of La³⁺ were used to regulate d-band states for promoting OER activity. Density of states calculations based on density functional theory revealed that La³⁺ doping produced upper shift of d-band center, which would induce stronger electronic interaction between surface Ni atoms and species of oxygen evolution reaction intermediates. Further density functional theory calculation illustrated that La³⁺ doped NiO possessed reduced Gibbs free energy in adsorbing species of OER intermediate. Predicted by theoretical calculations, trace La³⁺ was introduced into crystal lattice of NiO nanoparticles. The La³⁺ doped NiO nanocrystal showed much promoted OER activity than corresponding pristine NiO product. Further electrochemical analysis revealed that La³⁺ doping into NiO increased the intrinsic activity such as improved active sites and reduced charge transfer resistance. The in-situ Raman spectra suggested that NiO phase in La³⁺ doped NiO could be better maintained than pristine NiO during the OER. This work provides an effective strategy to tune the d-band center of NiO for efficient electrocatalytic OER.