4.7 Article

Bimetal-organic frameworks with coordinatively unsaturated metal sites for highly efficient Fenton-like catalysis

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 414, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.128669

Keywords

Fenton-like catalysis; Coordinatively unsaturated metal sites; CUMSs/MIL-101(Fe,Cu); H2O2 activation; Ciprofloxacin; Density functional theory

Funding

  1. Joint Research Fund for Overseas Chinese Scholars and Scholars in Hong Kong and Macao - National Natural Science Foundation of China [51925807, 51738013, 51729801]

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Recently, a new Fenton-like catalyst, CUMSs/MIL-101(Fe, Cu), with mixed valence of Fe(II)/Fe(III) and Cu(I)/Cu(II) as coordinatively unsaturated metal sites has been successfully synthesized and demonstrated enhanced degradation performance for ciprofloxacin compared to single iron catalyst in the neutral pH range. This work provides a new strategy for designing highly efficient, stable, and eco-friendly Fenton-like catalysts for superior environmental remediation efficiency across a wide pH range.
Recently, Fe-based metal-organic frameworks (Fe-MOFs) have been widely investigated as Fenton-like catalysts for environmental applications. However, their catalytic performance is limited by the insufficient number of Lewis acid sites for hydrogen peroxide (H2O2) activation and the slow Fe(III)-Fe(II) conversion. To overcome these limitations, coordinatively unsaturated iron-copper bimetallic sites may serve as Lewis acid sites, thus enhancing Fenton-like catalytic activity. Herein, we successfully synthesized a new Fenton-like catalyst of CUMSs/MIL-101(Fe,Cu), i.e., MIL-101 (MIL, Mat ' erial Institute Lavoisier) with mixed valence of Fe(II)/Fe(III) and Cu(I)/Cu(II) as coordinatively unsaturated metal sites (CUMSs). Further, we evaluated the performance of catalytically activating H2O2 for ciprofloxacin (CIP) degradation. The results indicate a rapid CIP degradation by dosing CUMSs/MIL-101(Fe,Cu) (0.1 g.L-1) and H2O2 (3 mM) in the neutral pH range, with a 20-fold higher apparent rate constant than in a MIL-101(Fe)/H2O2 system. Various conditions of initial pH, catalyst amount, H2O2 concentration, and coexisting anions on the CIP degradation were systematically investigated for optimizing CIP degradation. Furthermore, we identified the intermediates during the CIP degradation and proposed the possible degradation pathways. We concluded that the thermodynamically favorable reaction between Cu(I) and Fe(III) and p-cation interactions accelerate the redox cycles of Fe(II)/Fe(III) and Cu(I)/Cu(II) CUMSs and this effect improves the Fenton-like performance over a broad pH range. Density functional theory calculations further clarified the dissociation process and the corresponding energy barriers of H2O2 at the atomic level. This work offers a new way for designing highly efficient, stable and harmless Fenton-like catalysts for achieving excellent environmental remediation efficiency over a wide pH range.

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