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Engineered Oxygen Vacancies in NiCo2O4/BiOI Heterostructures for Enhanced Photocatalytic Pollutant Degradation

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Abstract To address the bottleneck issue of poor carrier separation and transfer efficiency in NiCo2O4 photocatalyst, a novel 1D/2D-rod on rose like NiCO2O4/BiOI nanohybrid with abundant OV’s was successfully synthesized using a single step hydrothermal method and employed to the photocatalytic degradation of Rhodamine B (RhB). The study revealed that the optimized NiCo2O4-OV/BiOI hybrid could possess superior photocatalytic degradation efficiency towards RhB degradation under visible light with rate constant that was 3.8 and 3.03 times greater than that of BiOI and NiCo2O4-OV. Experimental findings indicated that the formation NiCo2CO4-OV/BiOI heterojunction significantly improved the charge separation efficiency and facilitated the formation of surface OV’s. These OV’s enhanced photogenerated e--h+ separation and increased catalytic efficiency. Quenching experiments results confirmed that both holes and superoxide radicals are playing crucial roles in the degradation process. Thus, an oxygen vacancy and engineering NiCo2CO4-OV/BiOI heterojunction enhanced degradation mechanism was proposed, offering insights for the integration of advanced oxidation technologies and the development of catalytic materials to enhance pollutant degradation efficiency.
Title: Engineered Oxygen Vacancies in NiCo2O4/BiOI Heterostructures for Enhanced Photocatalytic Pollutant Degradation
Description:
Abstract To address the bottleneck issue of poor carrier separation and transfer efficiency in NiCo2O4 photocatalyst, a novel 1D/2D-rod on rose like NiCO2O4/BiOI nanohybrid with abundant OV’s was successfully synthesized using a single step hydrothermal method and employed to the photocatalytic degradation of Rhodamine B (RhB).
The study revealed that the optimized NiCo2O4-OV/BiOI hybrid could possess superior photocatalytic degradation efficiency towards RhB degradation under visible light with rate constant that was 3.
8 and 3.
03 times greater than that of BiOI and NiCo2O4-OV.
Experimental findings indicated that the formation NiCo2CO4-OV/BiOI heterojunction significantly improved the charge separation efficiency and facilitated the formation of surface OV’s.
These OV’s enhanced photogenerated e--h+ separation and increased catalytic efficiency.
Quenching experiments results confirmed that both holes and superoxide radicals are playing crucial roles in the degradation process.
Thus, an oxygen vacancy and engineering NiCo2CO4-OV/BiOI heterojunction enhanced degradation mechanism was proposed, offering insights for the integration of advanced oxidation technologies and the development of catalytic materials to enhance pollutant degradation efficiency.

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