Because of the limitations of traditional chlorine-based bactericidal water treatment, such as the formation of disinfection byproducts (DBPs) and resistance to chlorine, novel approaches and materials are required for effective disinfection of water. This study focuses on the development of a new sterilization material, Ag/NH2-MIL-125(Ti), which was designed to effectively inactivate Escherichia coli in water. The effectiveness of the as-designed material stems from the synergistic interactions between Ag nanoparticles (NPs) and photoactive metal-organic frameworks (MOFs). In this complex material, the MOFs play a critical role in dispersing and isolating the Ag NPs, thus preventing undesirable aggregation during bacterial inactivation. Simultaneously, Ag NPs enhance the photocatalytic performance of the MOFs. Sterilization experiments demonstrate the remarkable rapid E. coli inactivation performance of Ag/NH2-MIL-125(Ti) under illuminated and nonilluminated conditions. Within 25 min of visible light exposure, the as-prepared material achieves a >7-log E. coli reduction. In addition, Ag/NH2-MIL-125(Ti) efficiently decomposes acetic acid, which is the main DBP precursor, under visible light irradiation. Mechanistic investigations revealed that •O2- and h+ were the primary active substances responsible for the inactivation of E. coli and the decomposition of acetic acid, respectively.
Keywords: Ag nanoparticles; Ti-based metal−organic frameworks; bactericidal; cooperativity; photocatalysis.