Efficient production of singlet oxygen via dioxygen activation on Cu0 decorated MoS2 facilitates the elimination of oxytetracycline
Molecular oxygen (O<sub>2</sub>), a green oxidant, is applied in advanced oxidation processes, which represents one of the current focal points in water treatment research. However, achieving efficient and economical activation of O<sub>2</sub> remains a formidable challenge because of its spin-restricted nature. Herein, zero-valent copper (Cu<sup>0</sup>) modified molybdenum disulfide (MoS<sub>2</sub>) materials were applied as O<sub>2</sub> activators to degrade organic pollutants. The results showed that Cu<sup>0</sup>-MoS<sub>2</sub> could significantly enhance the activation of O<sub>2</sub> and thus accelerate the removal of oxytetracycline (OTC). Notably, 90.0 % of OTC was eliminated within 20 min in the Cu<sup>0</sup>-F-MoS<sub>2</sub> (Cu<sup>0</sup>-Flower-MoS<sub>2</sub>) /air system. Quenching experiments, XPS spectra, and DFT calculations confirmed <sup>•</sup>O<sub>2</sub><sup>-</sup> and <sup>1</sup>O<sub>2</sub> were pivotal reactive species, with both Mo and Cu playing essential roles. Specially, O<sub>2</sub> was activated by Cu<sup>0</sup>/Cu<sup>+</sup> to generate <sup>•</sup>O<sub>2</sub><sup>-</sup>, then <sup>•</sup>O<sub>2</sub><sup>-</sup> was oxidized by Mo<sup>6+</sup> of MoS<sub>2</sub> into <sup>1</sup>O<sub>2</sub>. This research offers an eco-friendly approach for eliminating organic substances by activating O<sub>2</sub>.
Authors
- Xiaoyu Zheng (ORCID: https://orcid.org/0000-0001-8685-5728)
- Liangguo Yan (ORCID: https://orcid.org/0000-0002-2721-0142)
- Yanfei Li (ORCID: https://orcid.org/0000-0002-7033-0414)
- Wen Song
- Xuguang Li (ORCID: https://orcid.org/0000-0002-3868-3439)
Institutions
- University of Jinan (CN)
Publication Details
- Journal
- Journal of Colloid and Interface Science
- Published
- 2024-10-28
- DOI
- https://doi.org/10.1016/j.jcis.2024.10.139
- Citations
- 8
- Primary Topic
- Advanced Photocatalysis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.82
Funders
- National Natural Science Foundation of China