Abstract

ABSTRACTThe existence of organic pollutants in aqueous media has become a vital issue and a critical threat to human health, where organic toxic dyes represent the major contaminants in wastewater. Over the past few years, photocatalytic techniques have garnered a lot of interest in dye removal from wastewater. In this study, a series of ErxTbxZn1 − 2xO nanophotocatalysts (where x = 0.00, 0.01, 0.03, and 0.05) were synthesized and coded as ZET0, ZET1, ZET2, and ZET3 NPs (nanoparticles). The chemical and physical characteristics of the NPs were investigated using Fourier‐transform infrared spectroscopy (FT‐IR), X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), energy‐dispersive X‐ray (EDX) spectroscopy, and ultraviolet–visible diffuse reflectance spectroscopy (UV–vis DRS) techniques. Further examination by performing photocatalytic experiments, ZET1 NPs demonstrated effective Rhodamine B (RhB) dye degradation within 60 min. It was found that the kinetic rate constant values were 0.008, 0.097, 0.050, and 0.040 min−1 for ZET0, ZET1, ZET2, and ZET3 NPs, respectively. Aside from their remarkable photocatalytic degradation efficiency, these ZET1 photocatalysts are highly stable even after five consecutive cycles. In addition, the active species test revealed that the primary oxidation species involved in the photocatalytic process are holes (h+) and hydroxyl radicals (•OH), and a possible photocatalytic mechanism for degrading RhB by ZET1 photocatalysts was tentatively proposed. The enhancement of the photocatalytic degradation efficiency is due to the low recombination rate of photogenerated charge carriers, as well as a strong synergistic impact of Tb, Er, and ZnO components. Thus, the current study could offer a versatile strategy for the design of new and effective nano photocatalysts for wastewater purification in the future.

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