RESUMEN
Within moderate band gap, g-C3N4 and CdS are both promising visible light driven photocatalysts. However, their intrinsic high recombination rate of photo-induced electron-hole pairs along with the poor susceptibility in photocorrosion of CdS is main limitations hindering their practical application. In this study, the CdS/g-C3N4 composites with various weight ratios of CdS to g-C3N4 were solvothermal prepared from the dispersion of components, g-C3N4 and CdS, in ethanol. The physicochemical characterizations demonstrate the success in the fabrication of well-dispersed CdS nanoparticles in the g-C3N4 matrix. The enhanced photocatalytic activity of the g-C3N4/CdS composite over the degradation of methylene blue under visible light was ascribed to the effective photo-induced electron-hole separation via the step scheme (S-scheme) pathway in which the main contribution of high oxidative hydroxyl radicals (â¢OH) was demonstrated. Furthermore, via S-scheme model, we also clarify the depletion of photo-induced holes on CdS which is ascribed as the reason for improvement in resistance to photocorrosion of composites.
RESUMEN
The SnO2/g-C3N4 composites were fabricated via an annealing mixture of g-C3N4 and SnO2, which were obtained from calcinating melamine and hydrothermal treatment of SnCl4 solution, respectively. The photocatalytic properties of g-C3N4/SnO2 were studied over the degradation of Rhodamine B (RhB) under visible light, which exhibits a significantly improved photocatalytic activity compared to the single components, g-C3N4 and SnO2. The enhancement in photocatalytic activity of SnO2/g-C3N4 could be described by the S-scheme pathway, in which the effective charge transfer between components is demonstrated toward the suppression in recombination of the photogenerated electron-hole pairs within redox potential conservation. Besides, a new criterion, photochemical space-time yield, was applied to evaluate the photocatalytic performance of our samples.