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Abstract In this work, Ag/BiVO4 heterostructural photocatalysts were developed in order to reveal exceptional structural-dependent photoinduced charge migration kinetics as well as the underlying photocatalytic antibacterial dynamic process. The structure-dependent interface of BiVO4 and Ag nanoparticles was successfully constructed to improve the photoinduced interface charge transfer efficiency and interface correlation. DFT calculation indicated that a net charge of about 0.33 e between Ag and tz-BiVO4 was achieved by extraordinary interface charge transfer, being far larger than that between Ag and ms-BiVO4. Larger net charge has consequences on mobility of charge carriers of tz-BiVO4 that can raise the migration and separation of charge carriers for Ag/tz-BiVO4 heterojunction. Fine interfacial contact between Ag and tz-BiVO4 led to the optimized photocatalytic performance toward E. coli inactivation, being predominately higher than that of tz-BiVO4, ms-BiVO4, and Ag/ms-BiVO4 catalysts. Besides photocatalytic activity, the thermocatalytic inactivation activity of Ag/tz-BiVO4 also exhibited a factor of about 7.2 and 3.1 times higher than that of tz-BiVO4 and Ag/ms-BiVO4. Trapping and EPR measurements suggested that the structural-dependent photocatalytic activity of Ag/BiVO4 mainly originated from the pronounced variation of the capability to produce H2O2 active species, where the capability of generating H2O2 over Ag/tz-BiVO4 is highly accelerated. Moreover, it cannot be ignored that this study provides an ideal candidate for many aspects, such as environmental and water pollution caused by pathogenic microorganisms and disinfection of medical materials, food packaging, household materials, and public places, etc. |
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