期刊
APPLIED SURFACE SCIENCE
卷 466, 期 -, 页码 637-646出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2018.10.074
关键词
Core-shell heterostructures; Metal-organic frameworks; Calcination; Catalytic degradation; Organic pollutants
类别
资金
- National Natural Science Foundation of China [21475095]
- Tianjin Natural Science Foundation [17JCTPJC47900]
The high performance of catalysts relies largely on the meticulous design of hierarchical hollow micro/nanostructures with more active sites and superb structural tenability. Herein, we developed a simple strategy to design and fabricate CoFe2O4/CuO (sub)microcages using core-shell dual-MOF heterostructures (Fe-II-Co PBAs@HKUST-1) as both the precursor and self-sacrificing template. The derivation of metal oxide composites from dual-MOF heterostructures is challenging, and this method could overcome the difficulty caused by the possible lattice mismatch between the different MOFs. Uniform core-shell dual-MOF structures Fe-II-Co PBAs@HKUST-1 were first fabricated and then converted to CoFe2O4/CuO (sub)microcages by thermal annealing in air. The resulting CoFe2O4/CuO (sub)microcages were extensively characterized and exhibited remarkable catalytic performance with an excellent stability and magnetic recyclability for the reduction of 4-nitrophenol to 4-aminophenol by NaBH4. In addition, CoFe2O4/CuO (sub)microcages were also found to be highly active for catalytic reduction of methylene blue (MB) by NaBH4 in an aqueous solution. The results show that CoFe2O4/CuO (sub)microcages have potential application for organic pollutants degradation and environmental rehabilitation.
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