Mechanistic investigations of single-walled carbon nanotube synthesis by ferrocene vapor decomposition in carbon monoxide

被引:72
作者
Anisimov, Anton S. [1 ,2 ]
Nasibulin, Albert G. [1 ,2 ]
Jiang, Hua [1 ,2 ]
Launois, Pascale [3 ]
Cambedouzou, Julien [3 ]
Shandakov, Sergey D. [1 ,2 ,4 ]
Kauppinen, Esko I. [1 ,2 ,5 ]
机构
[1] Aalto Univ, Dept Appl Phys, NanoMat Grp, Espoo 02015, Finland
[2] Aalto Univ, Ctr New Mat, Espoo 02015, Finland
[3] Univ Paris 11, CNRS, Phys Solides Lab, UMR 8502, F-91405 Orsay, France
[4] Kemerovo State Univ, Dept Phys, Lab Carbon NanoMat, Kemerovo 650043, Russia
[5] VTT Biotechnol, Espoo 02044, Finland
基金
芬兰科学院;
关键词
CATALYST PARTICLE; IRON PENTACARBONYL; GROWTH-MECHANISM; TEMPERATURE; KINETICS; METHANE; STATE; SIZE;
D O I
10.1016/j.carbon.2009.09.040
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The single-walled carbon nanotubes (SWCNTs) were synthesized by the carbon monoxide disproportionation reaction on Fe catalyst particles formed by ferrocene vapor decomposition in a laminar flow aerosol (floating catalyst) reactor. On the basis of in situ sampling of the product collected at different locations in the reactor, kinetics of the SWCNT growth and catalyst particle crystallinity were studied. Catalyst particles captured before SWCNT nucleation as well as inactive particles were determined to have cementite (Fe3C) phase, while particles with gamma- and alpha-Fe phases were found to be embedded in the SCWNTs. The growth rate in the temperature range from 804 to 915 degrees C was respectively varied from 0.67 to 2.7 mu m/s. The growth rate constant can be described by an Arrhenius dependence with an activation energy of E-a = 1.39 eV, which was attributed to the carbon diffusion in solid iron particles. CNT growth termination was explained by solid-liquid phase transition in the catalyst particles. A high temperature gradient in the reactor was found to not have any effect on the diameter during the SWCNT growth and as a result on the chirality of the growing SWCNTs. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:380 / 388
页数:9
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