Ag₃PO₄ decorated black urchin-like defective TiO₂ for rapid and long-term bacteria-killing under visible light.

Abstract

Both phototherapy via photocatalysts and physical puncture by artificial nanostructures are promising substitutes for antibiotics when treating drug-resistant bacterial infectious diseases. However, the photodynamic therapeutic efficacy of photocatalysts is seriously restricted by the rapid recombination of photogenerated electron-hole pairs. Meanwhile, the nanostructures of physical puncture are limited to two-dimensional (2D) platforms, and they cannot be fully used yet. Thus, this research developed a synergistic system of Ag₃PO₄ nanoparticles (NPs), decorated with black urchin-like defective TiO₂ (BU-TiO_2-X/Ag₃PO₄). These NPs had a decreased bandgap compared to BU-TiO_2-X, and BU-TiO_2-X/Ag₃PO₄ (3:1) exhibited the lowest bandgap and the highest separation efficiency for photogenerated electron-hole pairs. After combination with BU-TiO_2-X, the photostability of Ag₃PO₄ improved because the oxygen vacancy of BU-TiO_2-X retards the reduction of Ag⁺ in Ag₃PO₄ into Ag⁰, thus reducing its toxicity. In addition, the nanospikes on the surface of BU-TiO_2-X can, from all directions, physically puncture bacterial cells, thus assisting the hybrid's photodynamic therapeutic effects, alongside the small amount of Ag⁺ released from Ag₃PO₄. This achieves synergy, endowing the hybrid with high antibacterial efficacy of 99.76 ± 0.15% and 99.85 ± 0.09% against <i>Escherichia coli</i> and <i>Staphylococcus aureus</i>, respectively, after light irradiation for 20 min followed by darkness for 12 h. It is anticipated that these findings may bring new insight for developing synergistic treatment strategies against bacterial infectious diseases or pathogenic bacterial polluted environments.