Construction of novel Z-scheme Ag/ZnFe2O4/Ag/BiTa1-xVxO4 system with enhanced electron transfer capacity for visible light photocatalytic degradation of sulfanilamide.

Abstract

A novel Z-scheme system, Ag/ZnFe2O4/Ag/BiTa1-xVxO4 with enhanced electron transfer capacity was constructed for degrading sulfanilamide (SAM) using solar light. The photocatalytic activity of Ag/ZnFe2O4/Ag/BiTa1-xVxO4 was investigated. The effects of the mass ratio (ZnFe2O4:BiTaO4), doped V dose, Ag wt.% content, and irradiation time on the catalytic performance were evaluated. The reasonable mechanism of Ag/ZnFe2O4/Ag/BiTa1-xVxO4 solar photocatalytic degradation was also presented. These results reveal Ag/ZnFe2O4/Ag/BiTa1-xVxO4 possesses enhanced photocatalytic performance. The loaded Ag as electron mediator increases the electron transfer rate. Particularly, the doped V and the Fe ions from ZnFe2O4 form a powerful electron driving force, which enhances the electron transfer capacity. Ag/ZnFe2O4/Ag/BiTa1-xVxO4 shows optimal photocatalytic performance at 2.0 wt.% Ag and 0.5% doped V dose (ZnFe2O4:BiTaO4 = 1.0:0.5). Also, Ag/ZnFe2O4/Ag/BiTa1-xVxO4 exhibits high stability and repeatability in photocatalytic degradation. Several active species (•OH, •O2-, and h+) are produced in the Z-scheme photodegradation of SAM. These results on the enhanced photocatalytic activity of Ag/ZnFe2O4/Ag/BiTa1-xVxO4 are ascribed to synergistic photocatalytic effects of ZnFe2O4 and BiTa1-xVxO4 mediated through Ag and driven by doped V and Fe ions. Therefore, the Z-scheme Ag/ZnFe2O4/Ag/BiTa1-xVxO4 photocatalytic technology proves to be promising for the solar photocatalytic treatment of antibiotics under solar light.