纳米晶
选择性
甲基环戊烷
催化作用
金属有机骨架
环己烷
材料科学
化学工程
结晶度
纳米晶材料
多相催化
金属
化学
纳米技术
结晶学
物理化学
有机化学
吸附
工程类
作者
Kyungsu Na,Kyung Min Choi,Omar M. Yaghi,Gábor A. Somorjai
出处
期刊:Nano Letters
[American Chemical Society]
日期:2014-09-08
卷期号:14 (10): 5979-5983
被引量:244
摘要
The growth of nanocrystalline metal–organic frameworks (nMOFs) around metal nanocrystals (NCs) is useful in controlling the chemistry and metric of metal NCs. In this Letter, we show rare examples of nMOFs grown in monocrystalline form around metal NCs. Specifically, Pt NCs were subjected to reactions yielding Zr(IV) nMOFs [Zr6O4(OH)4(fumarate)6, MOF-801; Zr6O4(OH)4(BDC)6 (BDC = 1,4-benzenedicarboxylate), UiO-66; Zr6O4(OH)4(BPDC)6 (BPDC = 4,4′-biphenyldicarboxylate), UiO-67] as a single crystal within which the Pt NCs are embedded. These constructs (Pt⊂nMOF)nanocrystal are found to be active in gas-phase hydrogenative conversion of methylcyclopentane (MCP) and give unusual product selectivity. The Pt⊂nUiO-66 shows selectivity to C6-cyclic hydrocarbons such as cyclohexane and benzene that takes place with 100 °C lower temperature than the standard reaction (Pt-on-SiO2). We observe a pore size effect in the nMOF series where the small pore of Pt⊂nMOF-801 does not produce the same products, while the larger pore Pt⊂nUiO-67 catalyst provides the same products but with different selectivity. The (Pt⊂nMOF)nanocrystal spent catalyst is found to maintain the original crystallinity, and be recyclable without any byproduct residues.
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