Current understanding of the growth of carbon nanotubes in catalytic chemical vapour deposition

被引:464
|
作者
Jourdain, Vincent [1 ,2 ]
Bichara, Christophe [3 ,4 ]
机构
[1] Univ Montpellier 2, Lab Charles Coulomb, UMR 5221, F-34095 Montpellier, France
[2] CNRS, Lab Charles Coulomb, UMR 5221, F-34095 Montpellier, France
[3] CNRS, CINAM, F-13288 Marseille 9, France
[4] Aix Marseille Univ, F-13288 Marseille 9, France
关键词
SURFACE-ENERGY ANISOTROPY; METAL-SUPPORT INTERACTION; LOW-TEMPERATURE GROWTH; IN-SITU; SELECTIVE SYNTHESIS; PREFERENTIAL GROWTH; FILAMENTOUS CARBON; MOLECULAR-DYNAMICS; RAMAN-SPECTROSCOPY; DEPENDENT GROWTH;
D O I
10.1016/j.carbon.2013.02.046
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
Due to its higher degree of control and its scalability, catalytic chemical vapour deposition is now the prevailing synthesis method of carbon nanotubes. Catalytic chemical vapour deposition implies the catalytic conversion of a gaseous precursor into a solid material at the surface of reactive particles or of a continuous catalyst film acting as a template for the growing material. Significant progress has been made in the field of nanotube synthesis by this method although nanotube samples still generally suffer from a lack of structural control. This illustrates the fact that numerous aspects of the growth mechanism remain ill-understood. The first part of this review is dedicated to a summary of the general background useful for beginners in the field. This background relates to the carbon precursors, the catalyst nanoparticles, their interaction with carbonaceous compounds and their environment. The second part provides an updated review of the influence of the synthesis parameters on the features of nanotube samples: diameters, chirality, metal/semiconductor ratio, length, defect density and catalyst yield. The third part is devoted to important and still open questions, such as the mechanism of nanotube nucleation and the chiral selectivity, and to the hypotheses currently proposed to answer them. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2 / 39
页数:38
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