Iron phthalocyanine nanodots decorated ultra-thin porous carbon nitride: A combination of photocatalysis and Fenton reaction to achieve two-channel efficient tetracycline degradation.

Recent years, many scholars have been greatly intrigued by the large amounts of emerging antibiotics pollutants (such as tetracycline, penicillin, etc.) in natural water environments. Photo-Fenton oxidation, a highly advanced oxidation technique, has been seen as a promising way to effectively break down these pollutants by generating a great deal of reactive oxygen species (ROS). Herein, iron phthalocyanine nanodots (FePc)/ultra-thin porous carbon nitride (UPCN) nanocomposites were successfully prepared by thermal polymerization and calcination processes. In the system with a small amount (10 μL) of hydrogen peroxide (H 2 O 2) and natural pH conditions, the 1%-FePc/UPCN nanocatalcatalyst had the best degradation effect, and the TC removal rate reached 89% within 20 min and 99% within 60 min. The excellent performance of the nano-composites is ascribed to the large surface area, multiple active sites, small pore size, easy excitation and fast transfers of photogenerated carriers induced by π - π bond. In addition, the improvement of the degradation of TC is also due to the synergistic effect of the photocatalytic reaction center dominated by UPCN and Fenton reaction center dominated by FePc in the system, simultaneously. In this study, a synergistic dual-reaction center catalytic system was constructed to provide new insights and strategies for the degradation of organic pollutants in natural water environments. [Display omitted] • FePc/UPCN nanocomposite was successfully prepared by loading FePc nanodots on UPCN. • A small amount of H 2 O 2 (10 μL) was required for optimal performance. • At natural pH, 1%-FePc/UPCN photocatalyst showed the highest Photo-Fenton performance. [ABSTRACT FROM AUTHOR]