Search

Development of highly efficient and metal‐free photocatalysts for bacterial inactivation under natural light is a major challenge in photocatalytic antibiosis. Herein, we developed an acidizing solvent‐thermal approach for inserting a non‐conjugated ethylenediamine segment into the conjugated planes of 3,4,9,10‐perylene tetracarboxylic anhydride to generate a photocatalyst containing segregated π‐conjugation units (EDA‐PTCDA). Under natural light, EDA‐PTCDA achieved 99.9 % inactivation of Escherichia coli and Staphylococcus aureus (60 and 45 min), which is the highest efficiency among all the natural light antibacterial reports. The difference in the surface potential and excited charge density corroborated the possibility of a built‐in electron‐trap effect of the non‐conjugated segments of EDA‐PTCDA, thus forming a highly active EDA‐PTDA/bacteria interface. In addition, EDA‐PTCDA exhibited negligible toxicity and damage to normal tissue cells. This catalyst provides a new opportunity for photocatalytic antibiosis under natural light conditions. [ABSTRACT FROM AUTHOR]

Development of highly efficient and metal‐free photocatalysts for bacterial inactivation under natural light is a major challenge in photocatalytic antibiosis. Herein, we developed an acidizing solvent‐thermal approach for inserting a non‐conjugated ethylenediamine segment into the conjugated planes of 3,4,9,10‐perylene tetracarboxylic anhydride to generate a photocatalyst containing segregated π‐conjugation units (EDA‐PTCDA). Under natural light, EDA‐PTCDA achieved 99.9 % inactivation of Escherichia coli and Staphylococcus aureus (60 and 45 min), which is the highest efficiency among all the natural light antibacterial reports. The difference in the surface potential and excited charge density corroborated the possibility of a built‐in electron‐trap effect of the non‐conjugated segments of EDA‐PTCDA, thus forming a highly active EDA‐PTDA/bacteria interface. In addition, EDA‐PTCDA exhibited negligible toxicity and damage to normal tissue cells. This catalyst provides a new opportunity for photocatalytic antibiosis under natural light conditions. [ABSTRACT FROM AUTHOR]

Bi2MoO6 nanoflakes are synthesized via a normal hydrothermal method. Bi2MoO6 photocatalysts show lower photocatalytic activity for the degradation of methylene blue under visible light irradiation. In order to further enhance the degradation efficiency, Bi2MoO6 is used to activate the peroxymonosulfate for the degradation of methylene blue under visible light. Bi2MoO6 nanoflakes show excellent degradation efficiency in the Bi2MoO6/Vis/peroxymonosulfate (PMS) system. Moreover, the influences of PMS dosage, pH value, and inorganic anions on photodegradation are evaluated. The mechanism of activating peroxymonosulfate is proved by radical quenching experiment, which reveals that sulfate radicals govern the removal of methylene blue. [ABSTRACT FROM AUTHOR]