Ex Situ Method for Photoreduction of the Cadmium Ion from Terbium-Loaded Bismuth Vanadium Oxide.

Abstract

The photoreduction of Cd (II) to Cd (0) was performed using Bi4V2O11, which was tremendously enhanced by Tb3+-doped Bi4V2O11. The relationship between charge carrier isolation and light harvesting was studied in depth in this research, and a promising technique for fabricating effective photocatalysts for heavy metals was discovered. Lattice disorder effects due to size variance between V5+ and Tb3+ cations in Bi4V2O11 nanomaterials substituted with an invariable Tb3+ cation at different concentrations (x = 15, 20, and 25%). Bi4V2O11 and 15% Tb/Bi4V2O11 evidenced a coexistence of monoclinic (α-phase) with a CS/m symmetry, while 25% Tb/Bi4V2O11 was tetragonal (γ-phase) with an I4/mmm symmetry. Raman scattering experiments elucidated the changes in Bi4V2O11 lattice corresponding to oxygen motion, suggesting significant destabilization of the VO4 tetrahedra after addition of Tb3+. The SEM micrograph depicted a disparity in the microstructure with reduced grain size in 25% Tb/Bi4V2O11 samples. However, the TEM micrographs of 25% Tb/Bi4V2O11 nanomaterials revealed that crystallite sizes of 25–35 nm were obtained, presenting a single tetragonal phase, highly homogeneous in nature. Impedance spectroscopy was used to study the conductivity of these compounds in the temperature range of 300 °C. At 300 °C, the compounds with x = 25% showed a conductivity of 15.92 S cm–1. The conductivity values were found to be comparable with the highest values reported in the literature for similar compounds.