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Objective: To photodegrade Diuron with TiO2-Al2O3 nanomaterials supported on graphene nanoplatelets (GnPs) Design/methodology/approach: The synthesis of the materials was carried out by the sol-gel method under mild conditions. Subsequently, the obtained materials were subjected to thermal processing for structural stabilization and pulverized. Synthesized nanomaterials were then characterized by nitrogen adsorption/ desorption, X-ray diffraction, scanning electron microscopy, and Uv-Vis spectroscopy. Results: The adsorption/desorption results indicated that the ternary TiO2-Al2O3/GnPs nanomaterials were found to have complex porosity, which suggested that TiO2-Al2O3 was formed on agglomerated GnPs. X-ray diffraction data revealed that the anatase phase of TiO2 and the -Al2O3 phase coexist with the crystalline phase of graphene. The morphology of the materials indicates that the nanoplatelets were randomly dispersed in a continuous mixed oxide phase. About the UV analysis, the presence of GnPs at 1 wt % concentration reduces the band gap by 6%. Limitations on study/implications: The physical and chemical properties of GnPs make the material an excellent candidate for the degradation of pollutants by photocatalysis. Findings/conclusions: The addition of GnPs improved the Diuron degradation, probably by forming a nanostructured interface or heterojunction. [ABSTRACT FROM AUTHOR]

The present work reports a facile strategy to develop L-arginine mediated Zn doped graphitic carbon nitride (g-C3N4) and its enhanced photocatalytic activity. The physicochemical properties of Zn-doped g-C3N4 were studied extensively by XPS, UV–Vis, XRD, SEM and BET analysis. The studied properties of the photocatalyst were then correlated with its photocatalytic hydrogen production rates. Zn doping was evidenced by the presence of Zn-N peak from high-resolution core level XPS spectral analysis. Photocatalytic hydrogen evolution experiments revealed that, upon Zn doping, the hydrogen production rate of g-C3N4 was increased from 34.6 to 78.7 µmol/g.h, i.e. 2.3 times more. The enhancement in the photocatalytic properties after Zn doping was addressed by estimating changes in the positions of conduction band minimum and valence band maximum through XPS valence band spectral analysis. [ABSTRACT FROM AUTHOR]