Optimized Synthesis Strategy of Mxene-Loaded Graphitic Carbon Nitride (g-C3N4) for Enhanced Photocatalytic Degradation of Rhodamine B

Developing efficient photocatalysts is essential for sustainable wastewater treatment and tackling global water pollution. Graphitic carbon nitride (g-C3N4) is a promising material because it is active under visible light and chemically stable. However, its practical application is limited by fast recombination of charge carriers and a low surface area. In this study, we report a simple hydrothermal method to synthesize exfoliated porous g-C3N4 (E-PGCN) combined with Ti3C2 MXene to form a heterojunction composite that addresses these issues. Various characterization techniques (FTIR, XRD, XPS, SEM, BET) confirmed that adding MXene improves light absorption, increases surface area (53.7 m2/g for the composite versus 21.4 m2/g for bulk g-C3N4 (BGCN)), and enhances charge separation at the interface. Under UV-visible light irradiation with Rhodamine B (RhB) as the model pollutant, the E-PGCN/Ti3C2 MXene composite containing 3 wt% MXene demonstrated an impressive degradation efficiency of 93.2%. This performance is superior to BGCN (66.6%), E-PGCN (82.5%), and E-PGCN/Ti3C2 MXene-5 wt% composites (81%). This is due to the excess Mxene which caused agglomeration and reduced activity. Scavenger studies identified electron radicals as the dominant reactive species, with optimal activity at pH ~4.5. This enhanced performance, 1.4 times greater than BGCN and 1.13 times higher than E-PGCN, is ascribed to the synergistic interplay between the excellent electrical conductivity of MXene and the porous structural features of E-PGCN. This work highlights the importance of morphological engineering and heterojunction design for advancing metal-free photocatalysts, offering a scalable strategy for sustainable water purification.