TiO2-Bi2O3/(BiO)2CO3-reduced graphene oxide composite as an effective visible light photocatalyst for degradation of aqueous bisphenol A solutions

TiO2 nanorods (T) were combined with a narrow band gap semiconductor beta-Bi2O3 (B) to form a heterojunction, which makes it possible for TiO2 to become active as a photocatalyst also under visible light illumination. To further increase the photocatalytic activity of TiO2+ Bi2O3/(BiO)(2)CO3 (TB) composite, we used a hydrothermal procedure to link it with reduced graphene oxide (rGO). Structural, surface and electronic properties of the obtained catalysts were analyzed and correlated to their performance in photocatalytic oxidation of aqueous bisphenol A (BPA) solution conducted in a batch reactor under visible light illumination. XRD, FTIR, UV-vis DR spectroscopy and photocurrent measurements of visible light illuminated TB composite catalyst clearly showed that (i) beta-Bi2O3 acts as a photosensitizer for TiO2 and (BiO)(2)CO3 present in the TB composite, (ii) holes (h(+)) are photo-generated in valence band (VB) of beta-Bi2O3 and due to the beta-Bi2O3/TiO2 heterojunction transferred into VB of TiO2, (iii) p-n junction between beta-Bi2O3 and TiO2 allows the photo-generated electrons (e(-)) in the conduction band (CB) of beta-Bi2O3 to transfer to TiO2, and (iv) p-n junction between beta-Bi2O3 and (BiO)(2)CO3 allows the photogenerated Kelectrons in the conduction band of beta-Bi2O3 to transfer to (BiO)(2)CO3. This means that more charge carriers are available to participate in the catalytic visible-light triggered oxidation process for the degradation of organic pollutants dissolved in water. The highest photocurrent density was measured for multi-phase TBR (TB + rGO) composite, which indicates that visible-light generated charge carriers in TB composite are injected into the reduced graphene oxide. The latter acts as a web for charge carrier percolation and suppresses the recombination of electron-hole pairs, thus resulting in improved catalytic activity of TBR. The results of UV-vis DR spectroscopy and photocurrent density measurements were entirely in line with the results of photocatalytic oxidation of water dissolved bisphenol A (BPA) in batch reactor under visible light illumination.