Abstract

Taking advantage of the oil-water interface, we introduced Ag@AgCl quantum dots (QDs) onto 2D Sn3O4 nanosheets to fabricate a composite photocatalyst with a 3D flower-like structure (denoted as Ag@AgCl/Sn3O4). Using the degradation of tetracycline hydrochloride (TC-HCl) and methylene blue (MB) as the examples, the as-prepared Ag@AgCl/Sn3O4 composite with Ag@AgCl weight loading of 1% indicated 9.6 and 7.88 times higher photocatalytic activity than the Sn3O4 nanosheets. Within both degradation reactions, hydroxyl radicals (•OH) and superoxide radicals (•O2−) were identified as the critical oxidation intermediates based on radical trapping and electron spin resonance (ESR) experiments. The unique morphology and photoelectrochemical properties of the as-prepared composites suggested the introduced Ag@AgCl QDs cooperated with the Sn3O4 semiconductor to enhance the utilization of solar energy. Overall, the established heterojunction helped to reduce the transfer barrier of the photoinduced charge carriers, wherein the surface plasmonic resonance (SPR) of Ag nanoparticles was believed to take the main responsibility. The present work combines the Ag@AgCl-QDs and flower-like 3D Sn3O4 microspheres for the first time to achieve an impressive degrading rate of TC-HCl and MB at the Ag@AgCl weight loading as low as 1%.

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