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Mass Spectroscopy of Chemical Reaction of 3d Metal Clusters Involved in Chemical Vapor Deposition Synthesis of Carbon Nanotubes
Author(s) -
Shuhei Inoue,
Shigeo Maruyama
Publication year - 2008
Publication title -
japanese journal of applied physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.487
H-Index - 129
eISSN - 1347-4065
pISSN - 0021-4922
DOI - 10.1143/jjap.47.1931
Subject(s) - cobalt , dehydrogenation , carbon nanotube , chemisorption , chemistry , nickel , transition metal , fourier transform ion cyclotron resonance , cluster (spacecraft) , chemical reaction , chemical vapor deposition , inorganic chemistry , chemical engineering , analytical chemistry (journal) , materials science , catalysis , nanotechnology , ion , organic chemistry , computer science , programming language , engineering
The chemical reactions of transition metal clusters in the gas phase have aroused considerable scientific interest and are also of critical scientific importance. For example, these reactions are involved in the synthesis of single-walled carbon nanotubes, which are considered ideal materials because of their outstanding properties. Alcohol catalytic chemical vapor deposition (ACCVD) is one of the best synthetic processes for carbon nanotubes (CNTs); however, even the initial growth mechanism is still unclear, unlike those of other synthetic processes. In this study, we used a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer to determine the initial reactions of transition metal cluster ions (iron, cobalt, and nickel) that are typically adopted in the alcohol CVD process. Metal clusters with approximately 10-25 atoms each, generated by a pulsed laser ablation system in a supersonic-expansion cluster beam source, were directly carried into the FT-ICR cell. Subsequently, ethanol was introduced into the ICR cell. We observed two different results: one was simple chemisorption observed in the iron cluster and the other was dehydrogenated chemisorption observed in the nickel cluster; however, cobalt clusters exhibited both patterns, and a sequential reaction was observed. Furthermore, the dehydrogenation of ethanol on the cobalt cluster is fully described from isotope-labeled experiments.

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