Exploring the critical dependence of adsorption of various dyes on the degradation rate using Ln3+-​TiO2 surface under UV​/solar light

The degrdn. of structurally different anionic dyes like Alizarin Red S (ARS) Amaranth (AR)​, Brilliant Yellow (BY)​, Congo Red (CR)​, Fast Red (FR)​, Methyl orange (MO)​, and Methyl red (MR) were carried out using Ln3+ (Ln3+ = La3+, Ce3+ and Gd3+) doped TiO2 at different pH conditions under UV​/solar light. All the anionic dyes underwent rapid degrdn. at acidic pH, while resisted at alk. conditions due to the adsorptive tendency of these dyes on the catalyst surface at different pH conditions. Gd3+ (0.15 mol​%)​-​TiO2 exhibited better activity compared to other photocatalyst ascribed to half filled electronic configuration of Gd3+ ions. It is proposed that Ln3+ serves only as charge carrier traps under UV light, while it also act as visible light sensitizers under solar light. Irresp. of the catalyst and excitation source, the dye degrdn. followed the order: AR > FR > MO > MR > ARS > BY > CR. The results suggest that pre-​adsorption of the pollutant is vital for efficient photocatalysis which is dependent on the nature of the substituent's group attached to the dye mol