Lab-in-a-Shell: Encapsulating Metal Clusters for Size Sieving Catalysis

被引:150
作者
Qiao, Zhen-An [1 ]
Zhang, Pengfei [1 ]
Chai, Song-Hai [1 ]
Chi, Miaofang [2 ]
Veith, Gabriel M. [3 ]
Gallego, Nidia C. [3 ]
Kidder, Michelle [1 ]
Dai, Sheng [1 ,4 ]
机构
[1] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
[3] Oak Ridge Natl Lab, Div Mat Sci & Technol, Oak Ridge, TN 37831 USA
[4] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
关键词
SOLVENT-FREE OXIDATION; HETEROGENEOUS CATALYST; SELECTIVE OXIDATION; AEROBIC OXIDATION; NANOPARTICLES; ALCOHOLS; CARBON; GOLD; PD; NANOCLUSTERS;
D O I
10.1021/ja505903r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here we describe a lab-in-a-shell strategy for the preparation of multifunctional core shell nano-spheres consisting of a core of metal clusters and an outer microporous silica shell. Various metal clusters (e.g., Pd and Pt) were encapsulated and confined in the void space mediated by the entrapped polymer dots inside hollow silica nanospheres acting first as complexing agent for metal ions and additionally as encapsulator for dusters, limiting growth and suppressing the sintering. The Pd clusters encapsulated in hybrid core shell structures exhibit exceptional size-selective catalysis in allylic oxidations of substrates with the same reactive site but different molecular size (cyclohexene similar to 0.5 nm, cholesteryl acetate similar to 1.91 nm). The solvent-free aerobic oxidation of diverse hydrocarbons and alcohols was further carried out to illustrate the benefits of such an architecture in catalysis. High activity, outstanding thermal stability and good recyclability were observed over the core shell nanocatalyst.
引用
收藏
页码:11260 / 11263
页数:4
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