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Core-shell dual-MOF heterostructures derived magnetic CoFe_2O_4/CuO (sub) microcages with superior catalytic performance

机译:核-壳双MOF异质结构衍生的CoFe_2O_4 / CuO(sub)磁性微笼具有优异的催化性能

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摘要

The high performance of catalysts relies largely on the meticulous design of hierarchical hollow microanostructures 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.
机译:催化剂的高性能主要取决于具有更多活性位和出色结构韧性的分级空心微/纳米结构的精心设计。在这里,我们开发了一种简单的策略来设计和制造CoFe2O4 / CuO(亚)微笼,使用芯-壳双MOF异质结构(Fe-II-Co PBAs @ HKUST-1)作为前体和自我牺牲模板。从双MOF异质结构衍生金属氧化物复合材料具有挑战性,这种方法可以克服不同MOF之间可能存在的晶格失配所带来的困难。首先制造了均匀的核-壳双MOF结构Fe-II-Co PBAs @ HKUST-1,然后通过在空气中进行热退火将其转变为CoFe2O4 / CuO(亚)微笼。所得的CoFe2O4 / CuO(亚)微笼子得到了广泛的表征,并表现出显着的催化性能,具有优异的稳定性和磁可循环性,用于NaBH4将4-硝基苯酚还原为4-氨基苯酚。此外,还发现CoFe2O4 / CuO(亚)微笼对水溶液中NaBH4催化还原亚甲基蓝(MB)具有很高的活性。结果表明,CoFe2O4 / CuO(亚)微笼在有机污染物的降解和环境修复方面具有潜在的应用前景。

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