By combining the plasmon resonance of Ag nanoparticles and orientation effects of ZIF-8, as well as the visible-light activity of g-C₃N₄, we constructed a direct Z-scheme heterojunction with a co-existing Ag⁺/Ag⁰ system by an in situ coprecipitation method. The presence of Ag⁺/Ag⁰ on the surface of ZIF-8 was confirmed by the exchange of Ag⁺ and Zn²⁺ ions. This promoted the reduction of the band gap of ZIF-8, according to X-ray diffraction (XRD) and X-ray photoelectron spectroscopy. The results reveal that the 12 wt% Ag@ZIF-8/g-C₃N₄ nanocomposite presented the best adsorptive-photocatalytic activity for the degradation of multi-residue antibiotics under visible light irradiation for 60 min. Its degradation efficiency reached 90%, and its average apparent reaction rate constant was 10.27 times that of pure g-C₃N₄. In the radical scavenger experiments, ˙O₂ ^- and ˙OH were shown to be important in the process of photocatalytic degradation. In addition, we proposed a possible direct Z-scheme photocatalytic mechanism, that is, an internal electric field was formed to compensate the mediators between the interfaces of Ag@ZIF-8 and g-C₃N₄. This improvement can be attributed to the direct Z-scheme heterojunction system fabricated between Ag@ZIF-8 and g-C₃N₄. This can accelerate photogenerated electron-hole separation and the redox capability of Ag@ZIF-8/g-C₃N₄. The integration of the adsorption and photocatalytic degradation of various antibiotics is a promising approach. ZIF-8 has been widely used in the integrated adsorptive-photocatalytic removal of various antibiotics due to its large surface area, high orientation adsorption capacity. Therefore, this study provides new insights into the design of enhanced redox capacity for the efficient degradation of multiple antibiotics under visible-light irradiation.

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