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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.
Springer Science and Business Media LLC
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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