Efficient visible light-driven photodegradation of glyphosate utilizing Bi2WO6 with oxygen vacancies: Performance, mechanism, and toxicity assessment

Abstract

Global environmental deterioration poses a major risk to ecological security and human health, and emerging technologies are urgently needed to deal with it. Therefore, the exploitation of photocatalysts with favorable activity for efficient degradation of pesticide contaminants is one of the strategies to achieve environmental remediation. Herein, oxygen vacancy-rich Bi2WO6 (Ov-BWO) was prepared through a solvothermal method utilizing ethylene glycol (EG), which exhibited excellent photocatalytic efficiency in photodegradation of glyphosate. The formation of oxygen vacancies (Ovs) in Ov-BWO was demonstrated utilizing XPS and EPR. PL, TRPL, photocurrent tests, and EIS analyses revealed that Ovs accelerated effective transfer of photogenerated charge, extended lifetime of charge carriers, promoted production of active species and significantly improved the photocatalytic performance. Compared with the low-activity Bi2WO6 (BWO, 59.6%), Ov-BWO showed outstanding photocatalytic activity, achieving a degradation efficiency of 91% for glyphosate at 120 min of visible light irradiation. Moreover, Ov-BWO also displayed outstanding recyclable stability after four repeated uses. Based on the characterization of photoelectric properties, a feasible photocatalytic reaction was put forth, along with glyphosate degradation pathways. Furthermore, the degradation intermediates of glyphosate were analyzed in detail employing HPLC-MS. The toxicity assessment indicated that degraded products had been proven to be non-toxic to the ecological system. This work presents the potential of photocatalysts with Ovs for the photodegradation of pesticides, providing a viable strategy for environmental renovation.