Preparation and crystal structure of a new bismuth vanadate, Bi3.33(VO4)2O2

Single crystals of a new bismuth vanadate, Bi3.33(VO4)2O2 was prepared by hydrothermal reaction using a hydrated sodium bismuthate, NaBiO3·nH2O as one of the starting compounds. The crystal structure was determined by using single crystal X-ray diffraction data. This compound crystallizes in the triclinic space group P1¯ (#2) with a = 7.114(1), b = 7.844(2), c = 9.372(2) Å, α = 106.090(7), β = 94.468(7) and γ = 112.506(8)°, Z = 2 and the final R factors are R1 = 0.052 and wR2 = 0.14 for 2085 unique reflections. The crystal structure is composed by four bismuth atoms with the coordination number of 6 or 8 and two VO4 tetrahedra, and one of four bismuth atoms is statistically distributed in the splitting sites with the distance of 0.83 Å. This compound exhibited photocatalytic behavior for decomposition of phenol under visible light irradiation and its activity was less than that of monoclinic BiVO4.

Crystal structure of Bi3.33(VO4)2O2. Solid lines indicate the unit cell.Figure optionsDownload as PowerPoint slideHighlights
► We can prepare a new bismuth vanadate, Bi3.33(VO4)2O2 by hydrothermal reaction using a hydrated sodium bismuthate.
► We clarify that the crystal structure is composed by four bismuth atoms with the coordination number of 6 or 8 and two VO4 tetrahedra.
► This compound exhibited photocatalytic behavior for decomposition of phenol under visible light irradiation.