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Molybdenum (Mo) doped BiVO4 was fabricated via a simple electrospun method. Morphology, structure, chemical states and optical properties of the obtained catalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), N2 adsorption–desorption isotherms (BET) and photoluminescence spectrum (PL), respectively. The photocatalytic properties indicate that doping Mo into BiVO4 can enhance the photocatalytic activity and dark adsorption ability. The photocatalytic test suggests that the 1% Mo-BiVO4 shows the best photocatalytic activity, which is about three times higher than pure BiVO4. Meanwhile, 3% Mo-BiVO4 shows stronger dark adsorption than pure BiVO4 and 1% Mo-BiVO4. The enhancement in photocatalytic property should be ascribed to that BiVO4 with small amount of Mo doping could efficiently separate the photogenerated carries and improve the electronic conductivity. The high concentration doping would lead the crystal structure transformation from monoclinic to tetragonal phase, as well as the formation of MoO3 nanoparticles on the BiVO4 surface, which could also act as recombination centers to decrease the photocatalytic activity.

Novel carbon quantum dot (CQD)-modified BiOI photocatalysts were prepared via a facile hydrothermal process. The CQD-modified BiOI materials were characterized by multiple techniques. The CQD with an average size around several nanometers was distributed on the surface of BiOI microsphere. Its photocatalytic activity was investigated sufficiently by the photodegradation of methylene orange (MO). The results showed that the CQD/BiOI 1.5 wt.% sample exhibited the optimum photocatalytic activity, which was 2.5 times that of the pure BiOI. This improvement was attributed to the crucial role of CQDs, which could be acted as a photocenter for absorbing solar light, charge separation center for suppressing charge recombination.Electronic supplementary materialThe online version of this article (doi:10.1186/s11671-016-1262-7) contains supplementary material, which is available to authorized users.