A method
for efficiently catalyzing the oxygen evolution reaction
(OER) represents a top priority for water electrolysis due to its
multistep electron transfer pathway and sluggish kinetics. The OER
activity can be promoted by generating high valence transition-metal
species in the electrocatalysts. In the present work, a versatile
anion–cation double doped Co3O4 (Se/Ni-Co3O4) microtube architecture is innovatively fabricated
as an OER electrocatalyst, by combining reliable and template-free
solvothermal strategy and calcination treatment. The obtained Se/Ni-Co3O4 possesses some desirable properties for OER
including an attractive mesoporous structure, abundant exposed active
species associated with surface oxygen vacancies, and fast charge
transfer rate. By precisely exploring the redox reaction behavior,
it is found that the effective Se and Ni double doping could readily
promote the generation of active Co(IV) species. Consequently, the
obtained Se/Ni-Co3O4 electrocatalyst affords
a very good OER electrocatalytic activity with an onset potential
of 1.47 V, small Tafel slope (62.9 mV dec–1), and
excellent durability in alkaline solution, which is even superior
to that obtained in the benchmark RuO2. The novel strategy
introduced in this research may open a new opportunity for the rational
design of highly efficient Co3O4-based OER electrocatalysts.