Formation of uncapped nanometre-sized metal particles by decomposition of metal carbonyls in carbon nanotubes

被引:37
|
作者
Chamberlain, Thomas W. [1 ]
Zoberbier, Thilo [2 ]
Biskupek, Johannes [2 ]
Botos, Akos [1 ]
Kaiser, Ute [2 ]
Khlobystov, Andrei N. [1 ]
机构
[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
[2] Univ Ulm, Cent Facil Electron Microscopy, D-89081 Ulm, Germany
基金
欧洲研究理事会;
关键词
IONIC LIQUIDS ILS; NANOPARTICLES; GRAPHENE; PRECURSORS; REDUCTION; CATALYSIS; FUEL; STABILITY; RUTHENIUM; MOLECULES;
D O I
10.1039/c2sc01026g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbonyl complexes of transition metals (M-x(CO)(y), where x = 1, 2, or 3 and y 6, 10, or 12 for M = W, Re, or Os, respectively) inserted into single walled carbon nanotubes (SWNT, diameter 1.5 nm) transform into metallic nanoparticles (MNPs) under heat treatment or electron beam irradiation. The host-nanotube acts as an efficient template, controlling the growth of MNPs to similar to 1 nm in diameter. The only co-product of nanoparticle formation, carbon monoxide (CO) gas, creates pockets of high pressure between nanoparticles, thus preventing their collision and coalescence into larger structures. As a result, the MNPs stay largely spheroidal in shape and are uniformly distributed throughout the entire length of the SWNT. Despite their extremely small size (on average each MNP contains 30-90 atoms) and no protection of their surface by a capping layer of molecules, the metallic nanoparticles encapsulated in nanotubes are very stable under ambient conditions and even at elevated temperatures. Aberration-corrected high-resolution transmission electron microscopy reveals the crystalline nature of the MNPs, probes their interactions with the nanotube interior and illustrates the complex dynamics of confined MNPs in real-time and direct-space.
引用
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页码:1919 / 1924
页数:6
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