A novel 0D/3D Z-Scheme heterojunction ZnS/MIL-88(A) with significantly boosted photocatalytic activity toward tetracycline

Coupling two different photocatalytic materials to construct a heterojunction is a preferable strategy for obtaining the composite photocatalyst with high activity. Herein, a novel 0D/3D Z-scheme heterostructure ZnS/ MIL-88(A) was constructed by anchoring 0D ZnS nanoparticles on the surface of the 3D MIL-88(A). The prepared ZnS/MIL-88(A) was characterized by using FT-IR, XRD, SEM, UV-vis and XPS. The photodegradation of tetracycline (TC) was conducted under the irradiation of visible light to evaluate the photocatalytic performance of ZnS/MIL-88(A). The creation of the Z-scheme heterostructure between ZnS and MIL-88(A) enables ZnS/MIL-88 (A) to exhibit excellent visible-light absorption ability and dramatically boost separation and transfer of the photo-induced charge carriers. Compared with MIL-88(A), ZnS/MIL-88(A) shows prominently enhanced photocatalytic activity toward tetracycline, achieving a TC degradation rate of 94 %. The highest photodegradation rate constant (0.02083 min(-1)) of TC by ZnS/MIL-88(A) is 7.77 and 12.33 folds as large as those by MIL-88(A) and ZnS, respectively. After five cycles of reuse, ZnS/MIL-88(A) shows only a slightly decreased TC removal rate, presenting excellent photo-stability. Furthermore, the Z-scheme interfacial charge migration mode and the photocatalytic mechanism of ZnS/MIL-88(A) were discussed according to the band position as well as the identification result of the active species. The radicals center dot O-2(-) and center dot OH generated in photocatalysis serve as major reactive species to decompose TC. This work provides a new way for designing efficient composite photocatalysts.