摘要
In this study, a carbon quantum dots modified maghemite catalyst (CQDs@ γ -Fe 2 O 3 ) has been synthesized by a one-step solvothermal method for efficient persulfate (PDS) activation under visible light irradiation. Transmission electron microscopy (TEM), scanning electron microscopy (SEM) and UV–vis diffuse reflectance spectroscopy (UV–vis DRS) characterization indicated that the formation of heterojunction structure between CQDs and γ -Fe 2 O 3 effectively reduced the catalyst band gap ( E g ), favoring the separation rate of electrons and holes, leading to remarkable efficient sulfamethoxazole (SMX) degradation as compared to the dark-CQDs@ γ -Fe 2 O 3 /PDS and vis- γ -Fe 2 O 3 /PDS systems. The evolution of dissolved irons also demonstrated that CQDs could accelerate the in-situ reduction of surface-bounded Fe 3+ . Electron paramagnetic resonance (EPR) and radical scavenging experiments demonstrated that both OH and SO 4 − were generated in the reaction system, while OH was relatively more dominant than SO 4 − for SMX degradation. Finally, the reaction mechanism in the vis-CQDs@ γ -Fe 2 O 3 /PDS system was proposed involving an effective and accelerated heterogeneous-homogeneous iron cycle. CQDs would enrich the photo-generated electrons from γ -Fe 2 O 3 , causing efficient interfacial generation of surface-bond Fe 2+ and reduction of adsorbed Fe 3+ . This visible light induced iron cycle would eventually lead to effective activation of PDS as well as the efficient degradation of SMX.
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