Novel heterojunction photocatalysts with remarkable photocatalytic capabilities and durability for degrading recalcitrant contaminants are extremely desired; however, their development still remains quite challenging. In this study, a series of flower-like BiOI/BiOCOOH p–n heterojunctions were fabricated via a controlled in situ anion-exchange process. During the process, BiOI formation and even deposition on BiOCOOH microspheres with tight interfacial contact were realized. As expected, BiOI/BiOCOOH heterojunctions revealed remarkable enhancements in photocatalytic antibiotic degradation capacities under visible light irradiation compared with pristine BiOI and BiOCOOH. The best-performing BiOI/BiOCOOH heterojunction (i.e., IBOCH-2) showed much improved photocatalytic CIP degradation efficiency of approximately 81- and 3.9-fold greater than those of bare BiOI and BiOCOOH, respectively. The eminent photocatalytic performances were due not only to the enhanced capability in harvesting photon energies in visible light regions, but also the accelerated separation of electrons and holes boosted by the p–n heterojunction. Active species trapping tests demonstrated that superoxide free radicals (•O2−) and photo-generated holes (h+) were major active species for CIP degradation. Recycling experiments verified the good durability of BIBO-2 over four runs. The facile in situ synthesis route and excellent performance endow flower-like BiOI/BiOCOOH heterojunctions with a promising potential for actual environmental remediation.
In-situ construction of ZnIn2S4/CdIn2S4 2D/3D nano hetero-structure for enhanced visible-light-driven hydrogen production
