4.8 Article

Dissolved organic matter promotes photocatalytic degradation of refractory organic pollutants in water by forming hydrogen bonding with photocatalyst

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WATER RESEARCH
卷 242, 期 -, 页码 -

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2023.120297

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Photocatalysis; Refractory organic pollutants; Dissolved organic matter; Hydrogen bonding; Promoted degradation

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Removing refractory organic pollutants in real water using photocatalysis is challenging due to the quenching effect of dissolved organic matter (DOM) on photogenerated holes. This study presents a hydrogen bonding strategy to prevent hole quenching and even promote the photocatalytic degradation of refractory organic pollutants by forming hydrogen bonds between DOM and a hydroxylated S-scheme heterojunction photocatalyst. The formed hydrogen network stabilizes the excited-state of DOM and improves electron-hole separation, leading to the generation of more reactive oxygen species for pollutant removal.
Removing refractory organic pollutants in real water using photocatalysis is a great challenge because coexisting dissolved organic matter (DOM) can quench photogenerated holes and thus prevent generation of reactive oxygen species (ROS). Herein, for the first time, we develop a hydrogen bonding strategy to avoid the scavenging of photoexcited holes, by which DOM even promotes photocatalytic degradation of refractory organic pollutants. Theoretical calculations combined with experimental studies reveal the formation of hydrogen bonding between DOM and a hydroxylated S-scheme heterojunction photocatalyst (Mo-Se/OHNT) consisting of hydroxylated nitrogen doped TiO2 (OHNT) and molybdenum doped selenium (Mo-Se). The hydrogen bonding is demonstrated to change the interaction between DOM and Mo-Se/OHNT from DOM-Ti (IV) to a hydrogen bonded complexation through the hydroxyl/amine groups of DOM and the OHNT in Mo-Se/OHNT. The formed hydrogen network can stabilize excited-state of DOM and inject its electron to the conduction band rather than the valence band of the OHNT upon light irradiation, realizing the key to preventing hole quenching. The electron-hole separation in Mo-Se/OHNT is consequently improved for generating more ROS to be involved in removing refractory organic pollutants. Moreover, this hydrogen bonding strategy is generalized to nitrogen doped zinc oxide and graphitic carbon nitride and applies to real water. Our findings provide a new insight into handling the DOM problem for photocatalytic technology towards water and wastewater treatment.

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