Catalytic functions of Mo/Ni/MgO in the synthesis of thin carbon nanotubes

L.P. Zhou, K. Ohta, K. Kuroda, N. Lei, K. Matsuishi, Lizhen Gao, T. Matsumoto, J. Nakamura

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    Abstract

    The functions and structures of Mo/Ni/MgO catalysts in the synthesis of carbon nanotubes (CNTs) have been investigated by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Thin 2−5-walled CNTs with high purities (over 90%) have been successfully synthesized by catalytic decomposition of CH4 over Mo/Ni/MgO catalysts at 1073 K. It has been found that the yield of CNTs as well as the outer diameter or thickness correlates well with the contents of these three elements. The three components Mo, Ni, and MgO are all necessary to synthesize the thin CNTs at high yields since no catalytic activity was observed for CNT synthesis when one of these components was not present. The outer diameter of the CNTs increases from 4 to 13 nm and the thickness of graphene layers also increases with increasing Mo content at a fixed Ni content, while the inner diameter stays at 2−3 nm regardless of their contents. Furthermore, the average outer diameter is in good agreement with the average particle size of metal catalyst. That is, the thickness or the outer diameter can be controlled by selecting the composition of the Mo/Ni/MgO catalysts. XRD analyses have shown that Mo and Ni form a Mo−Ni alloy before CNT synthesis, while the Mo−Ni alloy phase is separated into Mo carbide and Ni. These alloy particles are supported on MgO cubic particles 15−20 nm in width. It has been found that only small Mo−Ni alloy particles 2−16 nm in size catalyze CNT synthesis, with larger particles over 15 nm exhibiting no activity. Mo carbide and Ni should play different roles in the synthesis of the thin CNTs, in which Ni is responsible for the dissociation of CH4 into carbon and Mo2C works as a carbon reservoir.
    Original languageEnglish
    Pages (from-to)4439-4447
    JournalThe Journal of Physical Chemistry Part B
    Volume109
    Issue number10
    DOIs
    Publication statusPublished - 2005

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