Efficient photoactivation of peroxymonosulfate by Z-scheme nitrogen-defect-rich NiCo2O4/g-C3N4 for rapid emerging pollutants degradation

Limited peroxymonosulfate (PMS, HSO4-) activation efficiency resulted from slow metal reduction has been a challenge in visible-light (vis) assisted sulfate radical-based oxidation. Herein, a Z-scheme photocatalyst composed of nitrogen-defect-rich graphitic carbon nitride nanosheets embedded with nickel cobaltate nanoparticles (NiCo2O4/g-C3N4-N-vac) was elaborately designed to accelerate Ni(III)/Ni(II) and Co(III)/Co(II) cycles for PMS activation in PMS/vis system. The NiCo2O4/g-C3N4-N-vac exhibited remarkable enhancement with a tetracycline hydrochloride (TCH) degradation rate constant (0.1168 min(-1)), higher than those of NiCo2O4/g-C3N4 (0.0724 min(-1)) and g-C3N4 (0.0233 min(-1)), respectively. Also, the removal efficiencies of 95.5%, 94.2%, 98.0% and 91.4% for carbamazepine, 4-chlorophenol, atrazine and p-nitrophenol were achieved within 30 min, respectively. Theoretical and experimental results suggested that nitrogen (N) vacancies modulated electric structure to build Z-scheme-charge-transfer platform for rapid reduction of Ni(III) and Co(III), thereby accelerating PMS activation for remarkable removal of emerging pollutants. NiCo2O4/g-C3N4-N-vac exhibited excellent stability and corresponding electrical energy per order (EE/O) in different water matrix was evaluated. Additionally, TCH degradation behavior, pathways and toxicity of products were analyzed, respectively. This work provided an novel paradigm to design the efficient photo-activator of PMS for environmental remediation.

Automated summary

The study designed a Z-scheme photocatalyst to enhance the degradation efficiency of tetracycline hydrochloride, achieving high removal rates for carbamazepine, 4-chlorophenol, atrazine, and p-nitrophenol.