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Harnessing Fe-Mo Atomic Interfaces for Boosted Electron Transfer and ROS Generation in Sustainable Pollutant
Lihong Liang1, Jiazhen Cao2, Zhuan Chen1
1Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry & Molecular Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
None:
Developing efficient and sustainable catalytic systems for persistent organic pollutant degradation remains a critical challenge in wastewater treatment. Herein, we present a novel FeMo0.5-OCN catalyst integrating iron clusters and molybdenum single atoms with oxygen coordination, which synergistically activates peroxymonosulfate (PMS) to generate reactive oxygen species (ROS), including sulfate radicals (SO4•-) and singlet oxygen (1O2), for enhanced pollutant degradation. Density functional theory (DFT) calculations and experimental studies reveal that Mo single atoms facilitate pollutant adsorption via oxygen coordination, while Fe clusters drive PMS activation, enabling efficient electron transfer and ROS generation. The FeMo0.5-OCN/PMS system achieves rapid degradation (>90% within 1 min) and high mineralization (73% TOC removal) of phenol, along with robust stability over 30 reaction cycles and broad pH adaptability (pH 2-11). Apart from phenol, this system demonstrates outstanding degradation efficiency for other phenolic contaminants as well. The practical applicability of the system is demonstrated by chemical oxygen demand (COD) removal efficiencies of 91, 44, and 33% for phenolic, high-salinity, and alcohol-containing wastewaters, respectively, outperforming conventional Fe2+/H2O2 systems and activated carbon treatments. Heterogeneous catalytic model quantifies the contribution of ROS and the mass transfer behaviors of pollutants at the solid-liquid interface. Sensitivity analysis confirms that the 1O2-facilitated generation of p-benzoquinone (p-BQ) is the rate-determining step in the overall reaction pathway. Life cycle assessment (LCA) confirms the system's superior environmental sustainability and cost-effectiveness compared to conventional Fenton systems (Fe2+/H2O2 and Fe2+/PMS), with minimal metal leaching. This work highlights the critical role of interfacial electronic interactions in catalytic design and provides a scalable strategy for durable, eco-friendly wastewater remediation.
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