Surface Plasmon Resonance Induced Photocatalysis in 2D/2D Graphene/g-C3N4 Heterostructure for Enhanced Degradation of Amine-Based Pharmaceuticals under Solar Light Illumination

Abstract

Pharmaceuticals, especially amine-based pharmaceuticals, such as nizatidine and ranitidine, contaminate water and resist water treatment. Here, different amounts of graphene sheets are coupled with g-C3N4 nanosheets (wt% ratio of 0.5, 1, 3 and 5 wt% of graphene) to verify the effect of surface plasmon resonance introduced to the g-C3N4 material. The synthesized materials were systematically examined by advanced analytical techniques. The prepared photocatalysts were used for the degradation of amine-based pharmaceuticals (nizatidine and ranitidine). The results show that by introducing only 3 wt% graphene to g-C3N4, the absorption ability in the visible and near-infrared regions dramatically enhanced. The absorption in the visible range was 50 times higher when compared to the pure sample. These absorption features suggest that the surfaces of the carbon nitride sheet are covered by the graphene nanosheet, which would effectively apply the LSPR properties for catalytic determinations. The enhancement in visible light absorption in the composite was confirmed by PL analysis, which showed greater inhibition of the electron-hole recombination process. The XRD showed a decrease in the (002) plan due to the presence of graphene, which prevents further stacking of carbon nitride layers. Accordingly, the Gr/g-C3N4 composite samples exhibited an enhancement in the photocatalytic performance, specifically for the 5% Gr/g-C3N4 sample, and close to 85% degradation was achieved within 20 min under solar irradiation. Therefore, applying the Gr/g-C3N4 for the degradation of a pharmaceutical can be taken into consideration as an alternative method for the removal of such pollutants during the water treatment process. This enhancement can be attributed to surface plasmon resonance-induced photocatalysis in a 2D/2D graphene/g-C3N4 heterostructure.