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Glyphosate is currently the most widely used herbicide in the world due to its broad-spectrum effectiveness and relatively low cost. However, its massive and prolonged application has raised serious environmental concerns. In this context, novel strategies for the effective degradation of glyphosate and its derivatives are urgently needed. One promising and sustainable approach is the use of the photocatalytic method. In this study, we explore a polyfunctional photocatalytic system capable of producing high-value compounds by oxidation of glyphosate and simultaneously obtaining H 2 , a clean energy carrier. Namely, both organic and inorganic valuable compounds have been obtained by the partial oxidation of glyphosate. The effectiveness of various TiO 2 -based commercial and home-prepared polycrystalline photocatalysts has been explored. Pt-TiO 2 or Cu 2 O-TiO 2 heterostructured samples have been also investigated. The photocatalysts showed stability over repeated cycles and maintained their activity, indicating their practical potential. Mechanistic studies suggest that photogenerated holes were primarily responsible for the oxidative degradation of glyphosate, while photoexcited electrons drove the reduction of protons to H 2 gas. Pt-Brookite, used for the first time in this reaction, resulted in the most active photocatalyst affording about 51% of glyphosate conversion and an H 2 production of 0.34 mM.
Umair et al. (Fri,) studied this question.