Silver Cluster Formation, Dynamics, and Chemistry in Metal-Organic Frameworks

被引:213
作者
Houk, Ronald J. T. [1 ]
Jacobs, Benjamin W. [1 ]
El Gabaly, Farid [1 ]
Chang, Noel N. [2 ]
Talin, A. Alec [3 ]
Graham, Dennis D. [4 ]
House, Stephen D. [4 ]
Robertson, Ian M. [4 ]
Allendorf, Mark D. [1 ]
机构
[1] Sandia Natl Labs, Livermore, CA 94551 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[3] NIST, Ctr Nanosci & Technol, Gaithersburg, MD 20899 USA
[4] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
关键词
NANOPARTICLES; COORDINATION; SPECTROSCOPY; AGNO3; MOF-5; IONS;
D O I
10.1021/nl901397k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthetic methods used to produce metal nanoparticles typically lead to 6 distribution of particle sizes. In addition, creation of the smallest clusters, with sizes of a few to tens of atoms, remains very challenging. Nanoporous metal-organic frameworks (MOFs) are a promising solution to these problems, since their long-range crystalline order creates completely uniform pore sizes with the potential for both steric and chemical stabilization. We report a systematic investigation of silver nanocluster formation within MOFs using three representative MOF templates. The as-synthesized clusters are spectroscopically consistent with dimensions <= 1 nm, with a significant fraction existing as Ag-3 clusters, as shown by electron paramagnetic resonance. Importantly, we show conclusively that very rapid TEM-induced MOF degradation leads to agglomeration and stable, easily imaged particles, explaining prior reports of particles larger than MOF pores. These results solve an important riddle concerning MOF-based templates and suggest that heterostructures composed of highly uniform arrays of nanoparticles within MOFs are feasible.
引用
收藏
页码:3413 / 3418
页数:6
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