Abstract

Photocatalytic disinfection is an eco-friendly strategy that uses solar energy to purify bacteria-contaminated water. However, improvements in photocatalysts tend to focus on thermodynamics while neglecting kinetic interactions that involve oxygen. Here, we propose the MOF-on-MOF heterojunction NR-HKUST-1@Cu/ZIF-8 (NH@CZ) for kinetic photocatalytic disinfection; the heterojunction reduced bacterial load by nearly 8-log within 20 min. The NH@CZ structure exhibits a high specific surface area with Cu2O8 and CuN4 sites that provide substantial oxygen storage capacity and binding sites. In vitro experiments demonstrated the effective delivery of oxygen to photocatalytic reactions via NH@CZ, leading to enhanced superoxide radical (·O2-) generation. Experimental analysis and theoretical calculations confirm that the formation of heterojunctions in NH@CZ provides an efficient pathway for oxygen reduction by reducing the energy barrier associated with oxygen adsorption. Mechanistic studies show that reactive oxygen species (ROS) disrupt bacterial cell membranes, resulting in the release of cellular contents (e.g., potassium ions and macromolecular proteins) and subsequent cell death. Furthermore, the oxygen-carrying NH@CZ killed all microorganisms in Wei River water samples within 45 min. The MOF-on-MOF heterojunction offers a promising pathway to enhance ROS generation and provides valuable insights into advances in water disinfection technology.

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