Xudong Lv , Baoshan Gu , Jinquan Yi , Peiyan Yang , Zhifeng Wang
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引用次数: 0
Abstract
Graphene oxide (GO) is a promising metal-free photocatalyst for the degradation of organic pollutants. In particular, GO and H2O2 exhibit a synergistic effect that significantly enhances the degradation efficiency of organic pollutants. However, the mechanism of reactive oxygen species (ROS) generation and transformation in the GO and H2O2 system (GO/H2O2) has not been reported. In this study, we prepared GO with photocatalytic activity under visible light. When targeting the reactive red X-3B (X-3B) as a pollutant, the synergistic efficiency of the GO/H2O2 was enhanced by 85.56%. We employed electron paramagnetic resonance (EPR) and free radical probe to conduct both qualitative and quantitative analyses of ROS. The results show that ·OH, ·O2− and 1O2 were produced in the GO, H2O2, and GO/H2O2 systems. The synergistic effect was mainly driven by the reaction of H2O2 and h+ produced by GO under visible light. h+ is the engine of the synergistic effect between GO and H2O2. The transformation relationships among ·OH, ·O2− and 1O2 in the GO, H2O2 and GO/H2O2 systems were investigated. The main free radicals in the degradation process were 1O2 and ·O2−. The influencing factors of the GO/H2O2 system were investigated, covering GO concentration, H2O2 concentration, pH value, X-3B concentration, and common water matrices. Notably, GO demonstrates excellent durability and mineralization capacity, maintaining superior photocatalytic performance even after 6 cycles. Moreover, during its application, the number of defects in GO increases, which improves the photocatalytic performance. This work clarified the underlying synergistic mechanism of ROS in GO/H2O2.
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