To enhance the photocatalytic activity of monoclinic scheelite (ms) BiVO4 for dye degradation, the heterostructured core (BiVO4)/shell (BiVO4:Eu3+) samples were synthesized by sol–gel method. The samples were characterized by UV–Vis diffuse… Click to show full abstract
To enhance the photocatalytic activity of monoclinic scheelite (ms) BiVO4 for dye degradation, the heterostructured core (BiVO4)/shell (BiVO4:Eu3+) samples were synthesized by sol–gel method. The samples were characterized by UV–Vis diffuse reflectance spectroscopy, X-ray diffraction (XRD) and X-ray photoelectron spectra (XPS). The results reveal that as-synthesized photocatalysts are characteristic of ms core/shell structure, responsive to visible light. The XPS spectra confirm that the doped Eu3+ mainly distributed in the outside layer of BiVO4 particle. The valence band (VB) spectra indicate the shell (BiVO4:Eu3+) exhibits a high carrier mobility. The core/shell photocatalysts showed higher photocatalytic activity than pure BiVO4 through degrading Rhodamine B and Methylene blue. The better performance of core/shell heterojunction mainly results from that the Eu3+ ions selectively present on shell layer, increasing the VB value of shell layer (forming a interface electric field with core) and carrier mobility. It is considered that the half-filled 7f–electron configuration of Eu3+ can improve the electron trapping and transfer. Besides, the low PL intensity and high SBET of BiVO4/BiVO4:Eu3+ contribute to enhanced photocatalytic performances.
               
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