Regulating oxygen vacancies in Co3O4 by combining solution reduction and Ni2+ impregnation for oxygen evolution reaction

Oxygen vacancies are considered to be an important factor to influence the electronic structure and charge transport of electrocatalysts in the field of energy chemistry. Various strategies focused on oxygen vacancy engineering are proved to be efficient for further improving the electrocatalytic performance of Co3O4. Herein, an optimal Co3O4 with rich oxygen vacancies have been synthesized via a two-step process combining solution reduction and Ni2+ impregnation. The as-prepared electrocatalyst exhibits an enhanced oxygen evolution performance with the overpotential of 330 mV at the current density of 10 mA cm(-2) in alkaline condition, which is 84 mV lower than that of pristine one. With the increasing of oxygen vacancies, the charge transfer efficiency and surface active area are relatively enhanced reflected by the Tafel slope and double-layer capacitance measurement. These results indicate that combination of solution reduction and heteroatom doping can be a valid way for efficient metal oxides-based electrocatalyst development by constructing higher concentration of oxygen vacancy.

Automated summary

Oxygen vacancies are considered important for the electronic structure and charge transport of electrocatalysts. We synthesized Co3O4 with rich oxygen vacancies and found that it exhibited enhanced oxygen evolution performance in alkaline conditions. Increasing oxygen vacancies can improve charge transfer efficiency and surface active area.