Spinel oxides are affordable transition-metal electrocatalytic
materials, but their low conductivity and intrinsic activity restrict
their wide application in electrolyzed water catalysts. In this study,
a series of heterojunction samples comprising phosphorus-doped spinel
oxides NiCo2O4 in collaboration with g-C3N4 (NCP
x
@C3N4, x = 0.25, 0.50, 0.75) were fabricated
through a straightforward mixture method for water splitting. Therein,
the NCP0.5@C3N4 electrocatalyst exhibits
remarkable performance compared to the other synthesized compounds,
demonstrating a small overpotential of 247 mV at 10 mA cm–2 for the oxygen evolution reaction (OER), a favorable Tafel slope
of 48 mV dec–1, and decent durability. The collaborative
interaction between phosphorus doping and g-C3N4 results in the creation of numerous oxygen defects, increasing the
electrochemically active surface area in NCP0.5@C3N4 and demonstrating a direct enhancement of the OER.
Density functional theory (DFT) calculations verified that the introduction
of phosphorus and its collaboration with g-C3N4 effectively regulated the electronic structure and optimized the
d-band center position. Based on the results, a resilient synergistic
interaction between NCP0.5 and C3N4 sheets contributes to the enhanced electrocatalytic activity of
NCP0.5@C3N4.