摘要
Surface defective or heterojunction sites of catalysts generally afford remarkable catalytic activity thanks to their high-surface-energy. Regularly-generating multiple defective sites on the surface of a catalyst is exceedingly promising in many reactions. In this study, we report an unexpected Co/Fe-Co planar hybrid composite nanosheet with serried surface defects including surface biphasic junction sites or defective holes. A facile thermal-induced process was applied to trigger the generation of defective sites on planar Co/Fe-Co hydroxides. Through a controlled thermal process, massive serried CoO nanocrystals were in situ dissolved out of the surface of cobalt hydroxide, while defective surface holes were formed on the Fe-doped Co(OH)2 nanosheets under a prolonged thermal procedure. The morphology and microscale structure of the resulting Co/Fe-Co hybrid 2-dimensional (2D) composites were systematically examined by virtue of various characterization techniques. As expected, the obtained surface defective Co/Fe-Co planar composites showed obviously enhanced catalytic activity in the Fenton-like reaction. Based on a catalytic study, we proved that the CoO nanocrystals densely-distributed on thinlayer Co(OH)2. Uniformly-introduced Fe heteroatoms in the inter-structure of Co(OH)2, along with the formed surface defective holes on Fe-Co hybrid composites, are synergistically responsible for increased catalytic removal efficiency of MB in the presence of peroxomonosulfate.
源语言 | 英语 |
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页(从-至) | 2065-2077 |
页数 | 13 |
期刊 | Materials Chemistry Frontiers |
卷 | 1 |
期 | 10 |
DOI | |
出版状态 | 已出版 - 10月 2017 |