Development of coupled semiconductor oxides makes a significant advancement in catalytic functional materials. In this article, we report the preparation of nanobundle-shaped BiVO4–ZnO photocatalyst by a simple hydrothermal process followed by thermal decomposition. The photocatalyst was characterized by X-ray powder diffraction (XRD), high-resolution scanning electron microscopy (HR-SEM), field emission scanning electron microscopy (FE-SEM), energy-dispersive spectroscopy (EDS), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), photoluminescence spectroscopy (PL), and UV–vis diffuse reflectance spectroscopy (DRS). The XRD pattern confirmed formation of monoclinic scheelite BiVO4 and the hexagonal wurtzite structure of ZnO. HR-SEM images show nanobundle-like structure, and the size of the nanospheres ranges from 20 to 40 nm. BiVO4–ZnO has increased absorption in the UV and visible region when compared to ZnO. The catalytic activity of BiVO4–ZnO was evaluated by the photodegradation of Acid Violet 7 (AV 7), Evens Blue (EB), and Reactive Red 120 (RR 120). The results revealed that the photocatalytic activity of BiVO4–ZnO was much higher than that of ZnO, BiVO4, and TiO2–P25 under natural sunlight. BiVO4–ZnO is more advantageous than ZnO and BiVO4 in the degradation of AV 7, EB, and RR 120 because it has maximum efficiency at neutral pH 7. BiVO4–ZnO was found to be stable and reusable without appreciable loss of catalytic activity up to four consecutive cycles. The self-cleaning property of BiVO4–ZnO has been evaluated using contact angle measurements. Our results provide some new insights on the performance of solar active photocatalysts on environmental remediation.

Heterostructrued Pr6O11–ZnO prepared by a simple hydrothermal process, shows enhanced solar photocatalytic activity for azo dye degradation, hydrophobicity and photoconductivity.

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In this article we report the fabrication of 3 wt% Dy 2 WO 6 doped ZnO via a template-free hydrothermal process and its photocatalytic activity against azo dyes Rhodamine-B (Rh-B) and Trypan Blue (TB) in solar light irradiation.The as prepared Dy 2 WO 6 doped ZnO was characterised by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), high resolution scanning electron microscopy (HR-SEM) field emission transmission electron microscopy (FE-TEM), X-ray photoelectron spectroscopy (XPS), diffused reflectance (DRS) and photoluminescence (PL) spectroscopy. The results suggested that rare earth tungstate doping, with Dy 2 WO 6 , on ZnO has a great influence on the photocatalytic activity. Dy 2 WO 6 -ZnO possesses high reusability without appreciable loss of catalytic activity up to four runs and exhibits higher electrocatalytic activity than the prepared ZnO for methanol electrooxidation in alkaline medium, revealing its promising potential as the anode catalyst in direct methanol fuel cells. Hydrophobicity of ZnO increases on doping with Dy 2 WO 6 .

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In the present study, ZnO modified with rare earth oxides GdxMn; M=Mo, V, W) were synthesized by hydrothermal process and their catalytic activity was tested in an oxidative cyclization reaction for the selective synthesis of quinazolinones. The catalysts were characterized by various techniques such as BET surface area analysis, XRD, SEM‐EDX, DSC‐TGA, ICP‐MS and elemental color mapping. 5 wt% Gd2MoO6/ZnO exhibited good catalytic activity and gave 60–91% of Quinazolin‐4(3H) ones in toluene. The catalysts could be reused at least four times without loss of catalytic activity.

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