Enhancing Organic Pollutant Degradation Efficiency through a Photocatalysis–Electro-Fenton System via MoS2 Crystal Morphology Regulation

A photocatalysis–electro-Fenton (PEF) system was constructed via molybdenum disulfide (MoS2) to remove tetracycline (TC) without an external oxidant supply and solution pH adjustment. In the system, original graphite felt (GF) was used as a cathode, from which H2O2 was in situ generated continuously...

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Veröffentlicht in:ACS applied materials & interfaces 2024-11, Vol.16 (45), p.61983-61994
Hauptverfasser: Zhang, Huan, Liu, Chang, Dong, Wenrong, Chen, Peng, Jia, Feifei, Song, Shaoxian
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Sprache:eng
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Zusammenfassung:A photocatalysis–electro-Fenton (PEF) system was constructed via molybdenum disulfide (MoS2) to remove tetracycline (TC) without an external oxidant supply and solution pH adjustment. In the system, original graphite felt (GF) was used as a cathode, from which H2O2 was in situ generated continuously under power. MoS2 was motivated by visible light to facilitate the cycle of Fe2+/Fe3+, enhancing the Fenton process to produce •OH. The experimental results showed that the system can increase the degradation rate of pollutants by more than 5 times. Moreover, the quenching and electron paramagnetic resonance (EPR) tests demonstrated that •OH was the dominant active species. X-ray photoelectron spectroscopy (XPS) characterization, Mo concentration, and cycle experiments proved the excellent catalytic activity and chemical stability of MoS2. It is worth mentioning that the photocatalytic performances of different morphologies of MoS2 (flower, flake, and radar) were compared. As a result, flower-like MoS2 exhibited a much superior photoresponse than flake and radar, which could accelerate the Fe2+/Fe3+ cycle further effectively. These findings highlight the morphology–performance relationship of MoS2 under a PEF system and the mechanisms of contaminant degradation, which is of great significance for developing photoelectric Fenton technology.
ISSN:1944-8244
1944-8252
1944-8252
DOI:10.1021/acsami.4c12136