期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 3, 期 15, 页码 8028-8033出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ta00030k
关键词
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资金
- National Natural Science Foundation of China [21322606, 21436005, 21406075]
- Doctoral Fund of Ministry of Education of China [20120172110012]
- Fundamental Research Funds for the Central Universities [D214244w]
- Guangdong Natural Science Foundation [2013B090500027, 10351064101000000]
- China Postdoctoral Science Foundation [2014M550437]
The encapsulation of metal nanoparticles (MNPs) into metal-organic frameworks has generated recent research because of the promising novel physical and chemical properties originating from synergetic interactions between MNPs and MOFs. However, the development of a facile one-step approach for the incorporation of tiny MNPs within MOFs without additional stabilizing agents and reductants remains a great challenge. Herein, we report a new and general synthesis strategy for MNPs@MOFs that allows preferential self-assembly of MOFs around the in situ formed MNP surface by directly mixing both the reactive metal (e. g., H2PtCl6) and MOF precursors in DMF. This in situ one-step assembly approach is applicable to various MOFs, affording well-defined Pt@MOF composites with highly dispersed naked Pt NPs in narrow diameter distribution. The resulting Pt@MOF nanocomposites exhibit excellent stability, significantly enhanced catalytic activity and selectivity as compared to the commercial Pt/C in liquid-phase aerobic oxidation of alcohols.
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