Understanding the Structural-Dependent Photocatalytic Antibacterial Activity: a Case Study of Ag Modified BiVO4

• Published in: Nanoscale research letters Vol. 15; no. 1; p. 152
• Main Authors: Guan, Hailin, Tian, Yuefeng, Dong, Alideertu, Su, Yiguo
• Format: Journal Article
• Language: English
• Published: New York Springer US 22.07.2020; Springer Nature B.V; SpringerOpen
• Subjects: Ag/BiVO4; Antibacterial activity; Bismuth oxides; Catalysts; Catalytic activity; Charge efficiency; Charge transfer; Chemistry and Materials Science; Current carriers; Deactivation; DFT calculation; Disinfection; E coli; E. coli inactivation; Food packaging; Heterojunctions; Hydrogen peroxide; Inactivation; Materials Science; Medical materials; Microorganisms; Molecular Medicine; Nano Express; Nanochemistry; Nanoparticles; Nanoscale Science and Technology; Nanotechnology; Nanotechnology and Microengineering; Photocatalysis; Reaction kinetics; Silver; Structural dependent; Vanadates; Water pollution; Structural dependent; DFT calculation; Photocatalysis; Ag/BiVO; inactivation
• ISSN: 1556-276X; 1931-7573; 1556-276X
• DOI: 10.1186/s11671-020-03380-3

In this work, Ag/BiVO 4 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 BiVO 4 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-BiVO 4 was achieved by extraordinary interface charge transfer, being far larger than that between Ag and ms-BiVO 4 . Larger net charge has consequences on mobility of charge carriers of tz-BiVO 4 that can raise the migration and separation of charge carriers for Ag/tz-BiVO 4 heterojunction. Fine interfacial contact between Ag and tz-BiVO 4 led to the optimized photocatalytic performance toward E. coli inactivation, being predominately higher than that of tz-BiVO 4 , ms-BiVO 4 , and Ag/ms-BiVO 4 catalysts. Besides photocatalytic activity, the thermocatalytic inactivation activity of Ag/tz-BiVO 4 also exhibited a factor of about 7.2 and 3.1 times higher than that of tz-BiVO 4 and Ag/ms-BiVO 4 . Trapping and EPR measurements suggested that the structural-dependent photocatalytic activity of Ag/BiVO 4 mainly originated from the pronounced variation of the capability to produce H 2 O 2 active species, where the capability of generating H 2 O 2 over Ag/tz-BiVO 4 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.