Facile route for C-N/Nb 2 O 5 nanonet synthesis based on 2-methylimidazole for visible-light driven photocatalytic degradation of Rhodamine B

Herein, we fabricated a C and N co-modified Nb O nanonet structure (C-N/Nb O NNs) from niobium oxalate using 2-methylimidazole (Hmim) as a source for C and N a simple hydrothermal route. The obtained nanonets are robust and cost-effective with excellent recycling stability. Compared with N-doped TiO...

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Veröffentlicht in:RSC advances 2019-12, Vol.9 (68), p.39561-39571
Hauptverfasser: Qaraah, Fahim A, Mahyoub, Samah A, Hafez, Mahmoud Elsayed, Xiu, Guangli
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Sprache:eng
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Zusammenfassung:Herein, we fabricated a C and N co-modified Nb O nanonet structure (C-N/Nb O NNs) from niobium oxalate using 2-methylimidazole (Hmim) as a source for C and N a simple hydrothermal route. The obtained nanonets are robust and cost-effective with excellent recycling stability. Compared with N-doped TiO (N-TiO ) and a Nb O control sample (Nb O -CS), the resulting nanonets exhibited the highest performance toward the photocatalytic degradation of Rhodamine B (RhB) upon visible light irradiation ( > 420 nm). Through this study, we revealed that the synergetic effects of C and N on the nanonet surface, which were effectively incorporated into the surface of the Nb O nanonet structure, not only remarkably enhanced the visible light response by decreasing the bandgap to 2.9 eV but also improved the light utilization efficiency and photo-induced electron-hole pair separation efficiency of our nanonet structure. We also proposed that the presence of carbonate species (CO ) and nitrogen species (NO ) increased the population of generated holes (h ) that had the key role in the photodegradation mechanism of RhB, suggesting reasonable importance for the modification of Nb O with C and N. This synergism offers a new view to reveal the origin of photodegradation processes, introducing h as a key intermediate. Our approach provides a new insight to design 2D nanostructures with potential applications in catalysis, solar energy conversion, and environmental protection.
ISSN:2046-2069
2046-2069
DOI:10.1039/C9RA07505D