The Ca@TiO2@g-C3N4 nanocomposite was synthesized using non-precious components via heat polymerization followed by an ultrasonic power technique. The nanocomposite was extensively characterized. The X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) investigations unequivocally demonstrated the successful synthesis of the Ca@TiO2@g-C3N4 nanostructures. By account of its small particle size of 6.1081 nm, narrow band gap energy of 2.82 eV, and visible light activity, it was able to photodegrade MG dye in an efficient manner, achieving a 99.9 % degradation rate. The photoluminescence measurement demonstrated efficient separation and transfer of charge carriers. The ternary photocatalyst’s activity can be attributed to the production of a S-scheme heterojunction at the interfaces of TiO2@g-C3N4, the generation of defects such as Ti3+ and Ovs through the surface interaction of Ca with TiO2, and the enlarged surface area of the photocatalyst. The ternary Ca@TiO2@g-C3N4 nanostructures demonstrated superior photodegradation of MG dye in comparison to pure g-C3N4 and binary TiO2@g-C3N4. A viable mechanism is also shown through active species trapping experiments using different scavengers, demonstrating that the photogenerated h+ and O2− are vital in the photodegradation reaction under visible light irradiation. Furthermore, the catalyst’s potential for industrial applications is enhanced by its utilization of inexpensive initial ingredients, straightforward synthesis process, and ability to harness solar light.
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