Citation: Anqi LI, Wenjing YANG, Xueming LI, Yanfong REN. Performance and mechanism of a foam Ti/FeCo-Fe2O3-CoFe2O4/SnO2-Sb anode for synergistic activation of peroxymonosulfate toward degradation of organic pollutants[J]. Chinese Journal of Inorganic Chemistry, ;2026, 42(5): 944-958. doi: 10.11862/CJIC.20250323 shu

Performance and mechanism of a foam Ti/FeCo-Fe2O3-CoFe2O4/SnO2-Sb anode for synergistic activation of peroxymonosulfate toward degradation of organic pollutants

  • Corresponding author: Yanfong REN, renyr@cque.edu.cn
  • Received Date: 22 October 2025
    Revised Date: 27 January 2026

Figures(10)

  • To address the limited utilization efficiency of reactive species in conventional single electrochemical systems, we developed an electrochemical activation platform (Ti/FeCoO/SnO2-Sb+PMS) that coupling peroxymonosulfate (PMS) with a Ti/FeCo-Fe2O3-CoFe2O4/SnO2-Sb (named as Ti/FeCoO/SnO2-Sb) composite anode. To overcome the inherent limitations of conventional SnO2-Sb anodes in interfacial reaction kinetics and long-term operational stability, we introduced FeCoO as a key interlayer to build a hierarchical composite electrode. This design leverages the synergistic Fe and Co dual-metal sites to tailor the interfacial microenvironment, thereby achieving simultaneous enhancement in PMS activation efficiency and system stability. Performance evaluation showed that, within the Ti/FeCoO/SnO2-Sb+PMS system, the Ti/Fe-Co/SnO2-Sb anode delivered the best removal and mineralization of methyl orange (MO), with the removal efficiency of chemical oxygen demand (COD) markedly higher than that of the control system. In addition, acidic conditions favor PMS activation and further accelerate the degradation kinetics of MO. Compared with the Ti/SnO2-Sb/PMS system without FeCoO middle layer, the Ti/FeCoO/SnO2-Sb composite exhibited a more pronounced overall performance advantage. Mechanistic studies combining electrochemical analyses, electron paramagnetic resonance (EPR), and density functional theory (DFT) calculations indicate that the improved performance mainly arises from the composite interface effectively promoting direct electron transfer (DET) and strengthening electrochemical PMS activation. During degradation, superoxide radical (·O2-), hydroxyl radical (·OH), sulfate radical (SO4·-), and singlet oxygen (1O2) generation act synergistically, enabling efficient disruption of the conjugated structure of MO and sustained deep oxidation.
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