Decoration of Pt on the metal free RGO-TiO2 composite photocatalyst for the enhanced photocatalytic hydrogen evolution and photocatalytic degradation of pharmaceutical pollutant β blocker

Abstract Easy synthesis of graphene based composite photocatalyst with the incorporation of minimal quantity of noble metals for the enhanced photocatalytic hydrogen evolution as well as photocatalytic degradation and mineralization of recalcitrant pollutants under solar irradiation is an urgent requirement from the clean energy and environment point of view all over the globe. Herein, we demonstrate the decoration of Pt by photodeposition method on the hydrothermally synthesized RGO-TiO 2 nanocomposite. The various photocatalysts synthesized were successfully characterized by XRD, FTIR, Raman, UV–visible absorption spectra, XPS, SEM and TEM techniques. The well characterized photocatalysts were further investigated for the photocatalytic hydrogen evolution studies of methanol water mixtures under UV as well as simulated solar light irradiation. The optimized Pt-RGO-TiO 2 (1 wt % Pt and 10 wt % RGO) composite was found to show 14 fold increase in the photocatalytic hydrogen evolution efficiency under UV light irradiation and 20 fold increase under simulated solar light irradiation as compared to bare TiO 2 under UV light irradiation. The ternary photocatalyst showed very good recycle and reuse capability up to 4 cycles. The optimized Pt-RGO-TiO 2 was further tested for the enhanced photocatalytic degradation and mineralization of pharmaceutical pollutant namely β blocker Propranolol under UV as well as simulated solar light irradiation. The obtained results showed 79% and 94% reduction in COD of Propranolol under UV and simulated solar light irradiation respectively. The appreciable enhancement in the photocatalytic activity of the Pt decorated RGO-TiO 2 photocatalyst as compared to bare TiO 2 under UV and simulated solar light can be attributed to the use of maximum range of solar spectrum along with their excellent properties of charge separation by RGO and Pt.