Abstract
The wide application of the Fenton reaction has been severely restricted by the requirement of continuous feeding of H2O2, the iron-slurry production, and the slow recycle rate of Fe3+/Fe2+. This work reports transforming type-II Fe2O3@2H-MoS2 heterostructures to a Z-scheme Fe2O3@C@1T/2H-MoS2 catalyst capable of photocatalytic in situ generation of H2O2 as an oxidant for the subsequent Fenton reaction. With MoS2 as a co-catalyst to improve the reduction from Fe3+ to Fe2+, the cascade process demonstrates high performance in oxidative degradation of organics (e.g., 100 mg L−1 tetracycline within 100 min). The in situ generated H2O2, with a yield as high as 1575 μmol g−1 h−1 in air-saturated methanol solution (75 vol%), accounts for 43.5% of the total degradation efficiency. The current system represents an effective solution to the challenges in the traditional Fenton reaction, holding great potential for organic pollutant degradation in wastewater.
| Original language | English |
|---|---|
| Pages (from-to) | 1991-2001 |
| Number of pages | 11 |
| Journal | Journal of Materials Chemistry A |
| Volume | 11 |
| Issue number | 4 |
| DOIs | |
| State | Published - 12 Dec 2022 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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