ENHANCED PLASMONIC ACTIVITY IN AG-MODIFIED MnO<sub>2</sub>/SiO<sub>2</sub> SPHERES FOR RAPID MITIGATION OF ANTIBIOTIC RESISTANCE
Ternary SiO 2 /MnO 2 –Ag composites were synthesized and evaluated as photocatalysts for the degradation of antibiotic Tetracycline (TC) in aqueous solution. Morphological and optical analyses demonstrated that MnO 2 nanoparticles were efficiently tailored on the adsorbed sites of SiO 2 spheres, while plasmonic metallic silver nanoparticles (Ag NPs) were coated on the surface of the SiO 2 /MnO 2 composite. The SiO 2 /MnO 2 –Ag ternary composition, as obtained, exhibited remarkable photocatalytic activity in the degradation of TC (91.3%) antibiotic, surpassing the performance of individual SiO 2 , MnO 2 , and SiO 2 /MnO 2 catalysts. This higher photocatalytic efficiency is primarily attributed to two key factors: enhanced photo-absorption capabilities facilitated by the presence of Ag nanoparticles, and the substantial mitigation of photoinduced electron and hole recombination through efficient charge transfer at the Schottky junction. SiO 2 plays a pivotal role by acting as a template that accelerates the separation of electron–hole pairs, while Ag metal serves as an electron sink, thereby bolstering interfacial charge transfer.
Authors
- Xiu-Jia Guan
- Shun‐Hsyung Chang (ORCID: https://orcid.org/0000-0002-9836-3234)
- Yu‐Hung Chen (ORCID: https://orcid.org/0000-0001-5403-3762)
- Kasimayan Uma (ORCID: https://orcid.org/0000-0002-2626-6283)
- Yu‐Ching Chen (ORCID: https://orcid.org/0009-0008-0865-841X)
- Lung‐Chien Chen (ORCID: https://orcid.org/0000-0001-5470-8491)
- Zong‐Liang Tseng (ORCID: https://orcid.org/0000-0002-8424-1914)
Institutions
- National Taipei University of Technology (TW)
- Ming Chi University of Technology (TW)
- National Kaohsiung University of Science and Technology (TW)
Publication Details
- Journal
- Surface Review and Letters
- Published
- 2025-02-21
- DOI
- https://doi.org/10.1142/s0218625x25400025
- Primary Topic
- Advanced Nanomaterials in Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00