SiO 2 @AuAg/PDA hybrid nanospheres with photo-thermally enhanced synergistic antibacterial and catalytic activity
Wastewater discharged from industrial, agricultural and livestock production contains a large number of harmful bacteria and organic pollutants, which usually cause serious harm to human health. Therefore, it is urgent to find a "one-stone-two-birds" strategy with good antimicrobial and po...
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Veröffentlicht in: | RSC advances 2024-01, Vol.14 (7), p.4518-4532 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Wastewater discharged from industrial, agricultural and livestock production contains a large number of harmful bacteria and organic pollutants, which usually cause serious harm to human health. Therefore, it is urgent to find a "one-stone-two-birds" strategy with good antimicrobial and pollutant degradation activity for treating waste water. In this paper, SiO
@AuAg/Polydopamine (SiO
@AuAg/PDA) core/shell nanospheres, which possessed synergistic "Ag
-release-photothermal" antibacterial and catalytic behaviors, have been successfully prepared
a simple
redox polymerization method. The SiO
@AuAg/PDA nanospheres showed good catalytic activity in reducing 4-nitrophenol to 4-aminophenol (0.576 min
mg
). Since the AuAg nanoclusters contain both gold and silver elements, they provided a high photothermal conversion efficiency (48.1%). Under NIR irradiation (808 nm, 2.5 W
), the catalytic kinetics were improved by 2.2 times. Besides the intrinsic Ag
-release, the photothermal behavior originating from the AuAg bimetallic nanoclusters and the PDA component of SiO
@AuAg/PDA also critically improved the antibacterial performance. Both
and
could be basically killed by SiO
@AuAg/PDA nanospheres at a concentration of 90 μg mL
under NIR irradiation. This "Ag
-release-photothermal" coupled sterilization offers a straightforward and effective approach to antimicrobial therapy, and further exhibits high potential in nanomedicine for combating bacterial contamination in environmental treatment and biological fields. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/d3ra07607e |