Ultrasonic chemical synthesis of hybrid mpg-C3N4/BiPO4 heterostructured photocatalysts with improved visible light photocatalytic activity

Highly efficient mpg-C3N4/BiPO4 heterostructured photocatalysts were successfully synthesized via a facile ultrasonic chemical method. The structure, morphology, surface composition and chemical state of mpg-C3N4/BiPO4 hybrid photocatalysts were characterized by XRD, TEM, FTIR and XPS, respectively. Their photocatalytic activity was evaluated under visible light, UV light and solar light irradiation against the photodegradatiori of rhodamine B (RhB). BiPO4 nanorod was anchored on the surface of mpg-C3N4 nanosheets and the strong electrostatic interaction between mpg-C3N4 and BiPO4 facilitated the formation of mpg-C3N4/BiPO4 heterostructure. Under visible light irradiation, O-center dot(2)- and h(+) were the two primary active species. BiPO4 served as an electron trap to efficiently promote the separation of photo generated electron-hole pairs. The electrons in the CB of both BiPO4 and mpg-C3N4 could react with O-2 adsorbed onto the surface of BiPO4/mpg-C3N4 and reduce it to form O-center dot(2)-, the holes left behind in the VB of mpg-C3N4 could not directly oxidize OH- or H2O to form (OH)-O-center dot. The 9.5CN/0.5BPO could degrade 92.3% of RhB in 30 min, which was about 1.3 times as high as that of mpg-C3N4. The TOC removal rate of 9.5CN/0.5BPO was 1.23 times higher than that of mpg-C3N4. Under UV light irradiation, O-center dot(2)-, h+ and (OH)-O-center dot were the primary active species, the inhibition degree followed the order BQ> EDTA-2Na >TBA. The electrons in the CB of both BiPO4 and mpg-C3N4 could react with O-2 to generate O-center dot(2)-, the holes in the VB of BiPO4 could react with OH- or H2O to produte (OH)-O-center dot. The 9.5CN/0.5BPO could degrade 94.3% of RhB in 6 min, which was approximately 4.2 times higher than that of BiPO4 and 1.5 times larger than that of mpg-C3N4. The TOC removal rate of 9.5CN/0.5BPO was 6.98 times higher than that of P25. HPLC analysis proved that the destruction of the conjugated structure of RhB would be the major process. Based on the experimental results, a possible charge transfer mechanism for the enhanced visible and UV light photocatalytic activity was proposed. (C) 2017 Elsevier B.V. All rights reserved.