Biofilm-Assisted Fabrication of Ag@SnO₂‑<i>g</i>‑C₃N₄ Nanostructures for Visible Light-Induced Photocatalysis and Photoelectrochemical Performance

Development of advanced materials with a benign environmentally friendly approach for heterogeneous visible light photocatalysis is always preferable. An environmentally favorable approach was used to anchor silver nanoparticles (Ag NPs) to tin oxide-decorated-graphitic carbon nitride (SnO2-g-C3N4) using a biofilm as a green reducing tool for the biogenic synthesis of 1–6 mM Ag@SnO2-g-C3N4 nanostructures (NSs). The fabricated NSs were characterized using sophisticated techniques. The developed Ag@SnO2-g-C3N4 NSs showed a well-defined spherical-shaped Ag NPs anchored to SnO2-g-C3N4 NSs. The synthesized NSs were applied for photocatalytic degradation of hazardous dyes and photoelectrochemical studies. A comparative investigation of Ag@SnO2-g-C3N4 NSs for the visible light-assisted photocatalytic degradation of Methylene blue (MB), Congo red (CR), and Rhodamine B (RhB) was performed. The photocatalytic degradation of MB, CR, and RhB reached ∼99% in 90 min, ∼98% in 60 min, and ∼94% in 240 min, respectively. The anchoring of Ag NPs to SnO2-g-C3N4 NSs further enhanced the visible light photocatalytic degradation of the dyes due to surface plasmon resonance and by lowering the recombination of the photogenerated electrons and holes. Further, high electron transfer ability of Ag@SnO2-g-C3N4 NSs was investigated by electrochemical impedance spectroscopy to understand the mechanistic insights of the excellent activity under visible light irradiation. Hence, the present study provides an environmentally benign approach for the synthesis and excellent visible light effective photocatalysis and photoelectrochemical performance

Environmentally Sustainable Fabrication of Ag@<i>g‑</i>C₃N₄ Nanostructures and Their Multifunctional Efficacy as Antibacterial Agents and Photocatalysts

Noble-metal silver (Ag) nanoparticles (NPs) anchored/decorated onto polymeric graphitic carbon nitride (<i>g</i>-C₃N₄) as nanostructures (NSs) were prepared using modest and environment-friendly synthesis method with a developed-single-strain biofilm as a reducing implement. The as-fabricated NSs were characterized using standard characterization techniques. The nanosized and uniform AgNPs were well deposited onto the sheet-like matrix of <i>g</i>-C₃N₄ and exhibited good antimicrobial activity and superior photodegradation of dyes methylene blue (MB) and rhodamine B (RhB) dyes under visible-light illumination. The Ag@<i>g</i>-C₃N₄ NSs exhibited active and effective bactericidal performance and a survival test in counter to <i>Escherichia coli</i>, <i>Staphylococcus aureus</i>, and <i>Pseudomonas aeruginosa.</i> The as-fabricated NSs also exhibited superior visible-light photodegradation of MB and RhB in much less time as compared to other reports. Ag@<i>g</i>-C₃N₄ NSs (3 mM) showed superior photocatalytic measurements under visible-light irradiation: ∼100% MB degradation and ∼89% of RhB degradation in 210 and 250 min, respectively. The obtained results indicate that the AgNPs were well deposited onto the <i>g</i>-C₃N₄ structure, which decreases the charge recombination rate of photogenerated electrons and holes and extends the performance of pure <i>g</i>-C₃N₄ under visible light. In conclusion, the as-fabricated Ag@<i>g</i>-C₃N₄ NSs are keen nanostructured materials that can be applied as antimicrobial materials and visible-light-induced photocatalysts