Abstract

In this study, a facile four-step hydrothermal method was utilized to deposit a core-shell structure on UiO-66(Zr/Ti) nanoflake (NFs) as a visible-light-driven photocatalyst. The core was magnetic Fe3O4 which served as a charge carrier coated with WO3 shell. The as-prepared photocatalyst was characterized by XRD, VSM, BET, FTIR, FE-SEM, UV–Vis-DRS, and PL techniques which proved successful deposition of Fe3O4@WO3 core/shell particle on UiO-66(Zr/Ti)-NFs. The obtained photocatalyst was subsequently applied for urea photo-oxidation. This magnetically recoverable photocatalyst exhibited superior activity due to its desirable band alignment, high stability, and generation of the photo-induced charge carriers, as well as providing a high surface area with low mass transfer resistance. Fe3O4 core acted as charge-carrier to transport the photogenerated charges of UiO-66(Zr/Ti)-NFs (electron-donor) to WO3 charge-collectors for effective photoconversion. The central composite design was applied to design the experiments matrix in which flow rate, pH, irradiation time, catalyst mass, and initial urea concentration were considered as operational factors. The optimized condition was found by defining the desirability function. 90% degradation percentage was achieved at 550 mL/min solution flowrate, pH = 7, 120 min irradiation time, 0.22 g UiO-66(Zr)-NFs-Fe3O4@WO3, and 40 mg/L of the initial concentration of urea with the desirability value of 0.89. Such a superior photocatalytic activity of UiO-66-Fe3O4@WO3 can be ascribed to the reclamation of Fe3O4 as a low bandgap carrier, which accelerated the conveyance of electrons and followed surpassing charge separation. Our present findings open a new strategy to produce a wide range of core-shell heterogeneous catalysts to be applied in photoreactors scale-up.

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