RESUMEN
Here, a novel method for synthesis of heterostructured TiO2-MoO3 (MT) nanosheets photocatalyst by utilizing a facile electrochemical method and examined it's photocatalytic activity by the degradation of tetracycline hydrochloride (TCH), a model of organic pollutants, in the presence of peroxymonosulfate (PMS) under solar light irradiation (SL) was reported for the first time. The influence of several factors on the degradation efficiency including the initial concentration of TCH, solution pH, catalyst dosage, PMS concentration, and the existence of inorganic anions was explored. The MT-15/PMS system displayed a promising photocatalytic performance and up to 97% of TCH was degraded in 90 min the rate of the degradation reaction of MT-15/PMS was the highest (0.05299 min-1) compared to 0.00251, 0.00337, 0.00546, 0.00735, 0.01337min-1of TiO2-P25, TiO2-P25/PMS, MoO3, MoO3/PMS, and MT-15 respectively. The enhancement can be attributed to several reasons. First, the 2D morphology of the optimized heterostructure photocatalyst plays a significant role in providing much more active sites on its surface. Next, the boosted light absorption efficiency and higher photoproduced electron-hole pair separation ability, induced by the unique direct transformation of photogenerated electrons from the valance band of TiO2 to the conduction band of MoO3 via the Ti-O-Mo bond formed at the interface of MT heterostructure. Finally, the appropriate accessible reactive sites for the activation of PMS together with the synergistic effect between activation of PMS and photocatalytic processes eased the production of active species for the degradation of pollutants. Based on the scavenger experiments and EPR analysis, hydroxide and sulfate radicals were found to be the dominant free radical active species in the degradation process. Furthermore, the synergistic degradation reaction mechanism was proposed.