Mechanistic aspects of carbon nanotube nucleation and growth

被引:90
作者
Little, RB [1 ]
机构
[1] Florida A&M Univ, Natl High Magnet Field Lab, Dept Chem, Tallahassee, FL 32307 USA
关键词
carbon nanotubes; tubular nanostructures; vaporization; nucleation;
D O I
10.1023/A:1024841621054
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The discovery, synthesis, characterization, and applicability of carbon nanotubes have produced tremendous excitement and interest among scientists and engineers. In particular, the use of these unique tubular nanostructures for new strong lightweight materials, nanoelectronics, fuel storage and cells, electron emitters and bio, scanning probe microscopy, and chemical sensing devices has created an intense effort to advance the synthesis so as to mass produce carbon nanotubes with control over diameter and helicity. The massive and controlled synthesis of this heralded nanostructure has been a great challenge. Although significant progress has advanced the preparation, more synthetic development is required. The syntheses have so far involved three main approaches: arc discharge vaporization, laser vaporization, and catalytic chemical vapor deposition. The synthetic trend has progressed to a point where further advancement with these techniques will require a better understanding of the mechanism of nucleation and growth. The mechanics of carbon nanotube nucleation and growth involve very complex and diverse phenomena occurring under extreme conditions and on the mesoscopic scale. As yet the detail mechanism is unknown. Difficulties with experimental probing and computational simulation have increased the mystery of this mechanism. This review presents an account of research on the synthesis of carbon nanotubes and the mechanism of formation. This overview includes all three mentioned synthetic approaches and hybrids thereof. On the basis of this broad account a comprehensive mechanism for carbon nanotube nucleation and growth naturally arises. This mechanism is qualitative and it hopes to inspire more quantitative exploration and synthetic advancement.
引用
收藏
页码:135 / 185
页数:51
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