The initial development of carbon nanotube synthesis revolved heavily around the use of 3d valence transition metals such as Fe, Ni, and Co. More recently, noble metals (e.g. Au) and poor metals (e.g. In, Pb) have been shown to also yield carbon nanotubes. In addition, various ceramics and semiconductors can serve as catalytic particles suitable for tube formation and in some cases hybrid metal/metal oxide systems are possible. All-carbon systems for carbon nanotube growth without any catalytic particles have also been demonstrated. These different growth systems are briefly examined in this article and serve to highlight the breadth of avenues available for carbon nanotube synthesis.
The current excitement in carbon nanotubes (CNTs) was triggered by Sumio Iijima's Nature publication in 1991 . At that time there was a considerable interest in developing the arc evaporation method, initially discovered by Huffman and Krätschmer , for the production of C60 in macroscopic amounts. Iijima analysed the deposit on the cathode and found macroscopic amounts of multi-walled carbon nanotubes (MWNTs) and facetted graphitic particles. The lack of fullerenes in the sample was unexpected. Moreover, the excitement at that time in carbon nanostructures, born out of the discovery of fullerenes  was a further favourable factor and so his publication drew significant attention. Iijima's next step was to see if he could fill these structures with transition metals. Transition metals were mixed into the graphitic electrodes and the arc evaporation process was run. The resultant product sprung another surprise. This time, a new form of carbon nanotube, namely, single-walled carbon nanotubes (SWNTs) with diameters between 1.1 and 1.3 nm were obtained . Almost at the exact same time Donald S. Bethune, at IBM research laboratory, made the same discovery (see Figure 1) . The discovery of SWNT was particularly exciting due to interesting structure-property correlations. In addition, it highlighted the use of transition metals as catalysts for carbon nanotube synthesis. Over the next years, a massive amount of synthesis routes and variations were developed. Most of these were based on the use of catalyst particles, including the chemical vapour deposition (CVD) route. CVD synthesis of CNT is facile and can be set up in laboratories without difficulty. Moreover, it is easily scaled up for mass production and so has developed into the most popular technique.
Metal catalyst particles
Vapor-grown CNT generally use metal catalyst particles and some even claim CNT synthesis requires a catalyst for their formation, despite Iijima's original work on MWNT synthesis never having used a catalyst. The use of metal catalysts and filamentous carbon from vapour-based routes has a long history dating back well before Iijima's landmark work, perhaps even as far back as 1889 . For the most part 3d valence transition metals such as Fe, Co and Ni were used for the catalytic growth of CNT. More recently, several groups have grown CNTs from metals such as Au, Ag and Cu [7–10] and poor metals, e.g. Pb, In [11, 12]. The conventional arguments for CNT growth are argued to occur in a similar manner to the model proposed for filamentous carbon growth by Baker et al.  (Figure 2) which is derived from the vapour-liquid-solid (VLS) theory developed by Wagner and Ellis to describe Si whisker formation . The model proposed that hydrocarbons adsorb on the metal particles and are catalytically decomposed. This results in carbon dissolving into the particle forming a liquid eutectic. Upon supersaturation, carbon precipitates in a tubular, crystalline form. However, various alternative models exist and it is likely that the appropriate description of growth depends on the synthesis route and conditions used. For example, it is argued that at low temperature CNT growth can occur through surface diffusion . In addition, most models assume thermal equilibrium conditions, although in practice, this is not so. In the case of noble metal catalyst particles, at temperatures where the VLS model is expected to be valid, they exhibit very low carbon solubility and negligible carbide formation. Zhou et al.  argue that low carbon solubility results in an increased precipitation rate. To grow carbon nanotubes, Lu and Liu  argue one needs to match the carbon supply rate to the tube formation rate.
Ceramic and semiconductor catalysts
Of the non-metallic catalysts for CNT, SiC is the most widely used and historically one of the first to be exploited. The early investigations involved the high temperature annealing (>1500°C) of SiC and was first demonstrated by Kusunoki et al. . An example of the CNT is provided in Figure 3. Kusunoki and co-workers showed that in low vacuum conditions the SiC decomposes through the following oxidation route:
The controlled oxidation process depletes Si at the surface, enabling the construction of CNTs. However, the formation of the initial caps at the nucleation stage has yet to be clarified . Some argue a transformation process of surface graphene layers [20, 21] or amorphous carbon  forms nucleation caps. Others argue the formation of convex structures on the surface enable initial cap formation [23–25]. Single-walled carbon nanotubes (SWNTs) can also be grown from SiC nanoparticles in CVD as was shown by Takagi . Botti et al. [27, 28] demonstrated laser annealing of SiC nanoparticles as a technique to obtain CNT.
The potential of semiconducting catalyst particles was first demonstrated by Uchino et al. [29, 30] in which carbon-doped SiGe islands on Si were used to grow CNT after chemical oxidation and annealing treatments. Growth of the CNT was argued to occur from Ge clusters.
This is due to the greater thermodynamic tendency of Si to be oxidized as compared to Ge. Thus, the oxidation treatment results in the formation of SiO2 and the segregation of Ge clusters. Takagi et al.  also showed that SWNT could be grown directly from Ge particles as well as from Si nanoparticles.
Numerous investigators have shown oxides are well suited for CNT growth. An early example was the use of MgO as the catalysts for SWNT formation via the laser evaporation route . More recently, Liu et al.  showed Al2O3 nanoparticles could be used to grow SWNT using an alcohol CVD route. Steiner et al.  showed both multi- and single-walled carbon nanotubes could be grown from zirconia. The use of magnesium borates can yield B-doped CNT (Figure 4) as was first demonstrated by Bystrzejewski et al. [33, 34].
In 2009, two groups showed SWNT formation using SiO2 nanoparticles [35, 36]. A little later Bachmatiuk et al. [37, 38] showed stacked cup CNT could be grown from amorphous SiO2 nano-particles. However, transmission electron microscopy (TEM), infrared (IR) and Raman spectroscopic studies showed the nano-particles at the root of the CNT to be SiC. Their data points to the carbo-thermal reduction of SiO2. This result is in contrast to X-ray photoemission studies (XPS) by Huang et al.  which did not show any carbide formation and hence they argued growth occurred from the SiO2 particles. Steiner et al.  also conducted XPS studies and also found no evidence for carbide formation when using zirconia as the catalyst. However, it should be noted that Bachmatiuk et al.  also found no carbide formation when using XPS despite other techniques clearly demonstrating the presence of carbides. This suggests XPS, which is a surface sensitive technique, may not be best suited to determine if oxides used as catalysts for CNT growth reduce to carbides or not during synthesis. Various other oxides, outside of those mentioned, including TiO2 and lanthanide oxides can also be used to grow carbon nanotubes . Templated CNT grown in porous alumina without catalyst particles have also been demonstrated . Further studies are required to better understand which oxide systems are stable and which are reducible. Previous studies of ours in which nano-crystalline oxides were subjected CVD reactions showed many oxides are stable, whilst others are not. These studies confirmed oxides are capable of graphitising carbon .
Hybrid metal/metal-oxide catalyst systems
Many of the oxides described above as catalytic nano-particles for CNT growth are often used as supports in supported catalyst CVD. Commonly used oxide supports are Al2O3, SiO2, TiO2 and MgO. All these oxides have been shown to grow CNT. Their role is primarily to stabilize the metal catalysts, viz. prevent coalescence. However, in oxide-supported metal catalysis it is well known that small clusters can have enhanced catalytic activity. A well-known example is Au, which is a bulk material is rather inert, but finely dispersed and deposited on oxides as small nano-clusters Au exhibits high catalytic ability (e.g. Haruta). This enhanced catalytic activity is generally accepted to occur at the circumference of the nano-cluster/support interface.
It is then natural to query if oxides and the catalyst/support interface play a role in the case of CNT grown from oxide-supported metal catalyst clusters. To this end, we conducted various studies on CNT grown from Fe and Co clusters supported on alumina. Whilst the studies showed a good correlation between the initial catalyst size and the CNT outer diameter, after synthesis the catalyst particles are found to lie within the core of the CNT and are elongated . In addition, the roots of the graphitic walls do not terminate on the metal particle but rather on the oxide support as shown in Figure 5. This highlights the diversity with which carbon nanotubes can grow, in that some base growth modes show the CNT is rooted at the metal catalyst particle  much like tip growth grown CNT  or in other cases from the oxide support [42, 43].
Another hybrid metal/metal-oxide example is the hydrocarbon dissociation over supported less active metal catalysts like Au and Cu, where it is argued that electron donation to the support creates d-vacancies for hydrocarbon dissociation .
All carbon systems
The formation of CNT on the cathode in the arc-discharge route can occur without catalyst addition as shown by the work of Bacon in 1957  and more recently by Iijima . Despite the huge impact of Iijima's 1991 Nature paper, the fact that no catalyst was required was largely ignored or forgotten. More recently, a broad array of growth routes using pure carbon systems without any catalyst particle addition have emerged. Takagi et al.  have shown that SWNT can be grown in CVD using nano-diamond particles as catalysts. Moreover, nano-diamond particles do not suffer from coalescence and sintering difficulties. Exciting strategies to open fullerenes and use them as nucleation caps for SWNT have also been demonstrated. Once the fullerenes have been opened they are subjected to a CVD process and grow tubes [49, 50]. The proposed growth mechanism is given in Figure 6. In a similar vein, the direct cloning of SWNT was shown by Liu and co-workers . The formation of CNT on graphitic surfaces has also been demonstrated in various works by Lin et al. [52, 53]. In these studies by Lin et al., it was shown that the early formation of amorphous nanohumps apparently serve as seed sites for the self-assembly of CNT.
Whilst significant strides have been made in understanding CNT synthesis, the mechanisms behind growth remain a highly debated issue. In part this is due to some mechanisms being presented as universal. The brief variety of synthesis strategies presented in this simple review alone, highlight the need for particular mechanisms for specific routes and conditions. It is generally accepted that VLS description presented by Baker et al.  for carbon filament growth is also applicable to carbon nanotube growth, at least when metal catalyst particles are employed. However, even in this case, there are inconsistencies. As Reilly and Whitten  pointed out, the so called catalyst poisoning has yet to be demonstrated. As they highlight, often it is argued that a metal catalyst particle coated with amorphous carbon is considered poisoned, yet when it is coated with graphitic carbon (CNT growth) it is not considered poisoned, viz. they are apparently still able to decompose hydrocarbons. This oddity is further illustrated by our studies in which the catalyst particles lie fully within the core of the CNT [42, 43]. Moreover, the ability of oxides to form graphene [40, 55] and CNT [26–38] with out any metal catalyst present further weakens the commonly accepted notion that the (metal) catalyst particle is required to decompose the hydrocarbon. Reilly and Whitten proposed a free radical condensate (FRC) forms which provides carbon species through a leaving group. The breaking of carbon-hydrogen or carbon-carbon bonds naturally form free-radicals in hydrocarbon pyrolysis, with each fragment keeping one electron to form two radicals. The presence of a radical in a hydrocarbon molecule enables rapid rearrangement of carbon bonds. This same argument can explain the nucleation of CNT from unstable nano-humps which form on graphitic surfaces which then eventually lead to the formation of multi-walled carbon nanotubes [52, 53]. Thus, in the FRC model, the catalyst particle's primary role is to serve as template for the formation of hemispherical caps at nucleation (as this reduces the high total surface energy of the particle caused by its high curvature). Thereafter, the catalyst may also provide an interface where carbon rearrangement may occur. However, this is not a prerequisite. Another surface, for example, an oxide support or simply unsaturated bonds at the edges of graphitic layers (e.g. open tube ends) can provide suitable sites for growth. Various studies provide experimental evidence for carbon addition to the edges of free standing graphitic edges [56–58]. In this scenario, carbon species are able to diffuse along the surface of graphitic layers which are then adsorbed at the edges. This self-assembling mechanism can explain the growth of cloned SWNT , SWNT nucleated from opened fullerenes [49, 50] and from MWNT grown on graphitic surfaces [52, 53]. In the case of CNT growth from stable oxides (oxides which are not reduced in the reaction), either in nano-particulate form or as the support material, the VLS theory is not valid since carbon dissolution is unlikely and probably occurs through surface diffusion processes. In the case of very small (<5 nm) non-metallic catalyst particles, the increased relative fraction of low-coordinated atoms could lead to surface saturation followed by carbon precipitation . On the other hand, where the oxide can be reduced to a carbide, as for example, the carbo-thermal reduction of SiO2 nanoparticles [37, 38], bulk carbon dissolution and precipitation in a manner similar to the VLS theory may be relevant (e.g. Figure 7).
In short, there appear to be a variety of growth modes and investigating each is complicated. Ex situ studies by definition means the catalysts have had time to relax and re-crystallize before being subjected to any investigative method. Hence, ex situ studies are necessarily limited in that they cannot unequivocally testify to circumstances during growth. On the back of this some argue in situ measurements as the only way forward. However, these routes present key limitations such as the need to work at very low pressures, well beyond any conventional or commercial route would use, as is the case for TEM and XPS in situ studies. Moreover, in in situ TEM only tiny sample sizes are examined and in the case of XPS in situ examinations, as already discussed above, the technique is surface sensitive and hence provides limited information on the catalyst during growth. Another area to investigate is how nature produces carbon nanotubes. Surprisingly, there is little evidence on planet Earth for their formation with only a few examples of MWNT and none for SWNT . However, CNT may form more readily in outer space. Graphite whiskers have been found in high-temperature components of meteorites . In addition, it has been proposed they can form in protostellar nebulae via Fischer-Tropsch-type catalytic reactions [61, 62]. Recent experiments by the same group investigating the potential of Fischer-Tropsch and Haber-Bosch type reactions appear to support this hypothesis . Thus, it is the collective data from both ex situ and in situ examinations that are important; however, the limitations of each implemented technique, and the specifics of the synthesis route in question must be considered as there is no single universal growth mode.
There remains a fair amount of controversy in explaining carbon nanotube growth; this in part is due to the sheer number of possible synthesis routes and the fact that there is no single universal growth mode. Even so, tremendous advances have been made. This includes the development of new catalyst systems and even catalyst-free systems. Nonetheless the successful integration of CNT into applications and large-scale production processes remains limited and is dependant on the understanding of several fundamental issues. Some of these issues are highlighted by the disparate catalyst and catalyst free options available which raise new questions on nucleation and growth as well as the role of supports in supported catalysts. In some sense the rapid development of graphene may render CNT less important, for example, in the integration of carbon nanotubes in integrated circuit manufacturing, however, many of the questions raised in understanding carbon nanotube growth are directly relevant to graphene also.
chemical vapour deposition
free radical condensate
multi-walled carbon nanotubes
single-walled carbon nanotubes
transmission electron microscopy
X-ray photoemission studies.
Iijima S: Helical microtubules of graphitic carbon. Nature 1991, 354: 56. 10.1038/354056a0
Krätschmer W, Lamb LD, Fostiropoulos F, Huffman D: Solid C 60 : a new form of carbon. Nature 1990, 347: 354.
Kroto HW, Heath JR, O'Brien SC, Curl RF, Smalley RE: C 60 : Buckminsterfullerene. Nature 1985, 318: 162. 10.1038/318162a0
Iijima S, Ichihaschi T: Single-shell carbon nanotubes of 1-nm diameter. Nature 1993, 363: 603. 10.1038/363603a0
Bethune DS, Kaing CH, de Vries MS, Gorman G, Savoy R, Vazquez J, Beyers R: Cobalt-catalysed growth of carbon nanotubes with single-atomic-layer walls. Nature 1993, 363: 605. 10.1038/363605a0
Hughes TV, Chambers CR: Manufacture of Carbon Filaments. US Patent 405480 (1889)
Takagi D, Homma Y, Hibino H, Suzuki S, Kobayashi Y: Single-Walled Carbon Nanotube Growth from Highly Activated Metal Nanoparticles. Nano Lett 2006, 6: 2642. 10.1021/nl061797g
Takagi D, Kobayashi Y, Hibino H, Suzuki S, Homma Y: Mechanism of Gold-Catalyzed Carbon Material Growth. Nano Lett 2008, 8: 832. 10.1021/nl0728930
Rümmeli MH, Grüneis A, Löffler M, Jost M, Schönfelder R, Kramberger C, Grimm D, Gemming T, Barreiro A, Borowiak-Palen E, Kalbac M, Ayala P, Hübers H-W, Büchner B, Pichler T: Novel catalysts for low temperature synthesis of single wall carbon nanotubes. Phys Stat Sol B 2006, 243: 3101.
Borowiak-Palen E, Steplewska A, Rümmeli MH: On the use of Cu catalysts for tailoring carbon nanostructures in alcohol-CVD. Phys Stat Sol B 2009, 246: 2448. 10.1002/pssb.200982263
Rümmeli MH, Borowiak-Palen E, Gemming T, Pichler T, Knupfer M, Kalbac M, Dunsch L, Jost O, Silva SRP, Pompe W, Büchner B: Novel Catalysts, Room Temperature, and the Importance of Oxygen for the Synthesis of Single-Walled Carbon Nanotubes. Nano Lett 2005, 5(7):1209.
Bachmatiuk A, Schäffel F, Placha D, Martynkova GS, Ioannides N, Gemming T, Pichler T, Kalenczuk RJ, Borowiak-Palen E, Rümmeli MH: Tuning carbon nanotubes through poor metal addition to iron catalysts in CVD. Fuller Nanotubes Carbon Nanostruct 2010, 18: 703.
Baker T: Formation of filamentous carbon. Chem Ind (London) 1982, 18: 698.
Wagner RS, Ellis WC: Vapor-liquid-solid mechanism of single crystal growth. Appl Phys Lett 1964, 4: 89. 10.1063/1.1753975
Hofmann S, Csányi G, Ferrari AC, Payne MC, Robertson J: Surface Diffusion: The Low Activation Energy Path for Nanotube Growth. Phys Rev Lett 2005, 95: 036101. 10.1103/PhysRevLett.95.036101
Zhou W, Han Z, Wang J, Zhang Y, Jin Z, Sun Z, Zhang Y, Yan C, Li Y: Copper Catalyzing Growth of Single-Walled Carbon Nanotubes on Substrates. Nano Lett 2006, 6: 2987. 10.1021/nl061871v
Lu C, Liu J: Controlling the Diameter of Carbon Nanotubes in Chemical Vapor Deposition Method by Carbon Feeding. J Phys Chem B 2006, 110: 20254. 10.1021/jp0632283
Kusunoki M, Rokkaku M, Suzuki T: Epitaxial carbon nanotube film self-organized by sublimation decomposition of silicon carbide. Appl Phys Lett 1997, 71: 2620. 10.1063/1.120158
Kusonoki M, Suzuki T, Honjo C, Usami H, Kato H: Closed-packed and well-aligned carbon nanotube films on SiC. J Phys D 40: 6278. 10.1088/0022-3727/40/20/S12
Kusunoki M, Suzuki T, Kaneko K, Ito M: Formation of self-aligned carbon nanotube films by surface decomposition of silicon carbide. Philos Mag Lett 1999, 79: 153. 10.1080/095008399177381
Watanabe H, Hisada Y, Murainakano S, Tanaka N: In situ observation of the initial growth process of carbon nanotubes by time-resolved high resolution transmission electron microscopy. J Microsc 2001, 203: 40. 10.1046/j.1365-2818.2001.00902.x
Kusunoki M, Suzuki T, Hirayama T, Shibata N: A formation mechanism of carbon nanotube films on SiC(0001). Appl Phys Lett 2000, 77: 531. 10.1063/1.127034
Konishi H, Matsuoka H, Toyama N, Naitoh M, Nishigaki S, Kusunoki M: Growth control of carbon nanotubes on silicon carbide surfaces using the laser irradiation effect. Thin Solid Films 2004, 464: 295. 10.1016/j.tsf.2004.06.002
Hayashi K, Mizuno S, Tanaka S, Toyoda H, Tochihara H, Suemune I: Nucleation Stages of Carbon Nanotubes on SiC(0001) by Surface Decomposition. Jpn J Appl Phys 2005, 44: L803. 10.1143/JJAP.44.L803
Maruyama T, Bang H, Kawamura Y, Fujita N, Tanioka K, Shiraiwa T, Hozumi Y, Naritsuka S, Kusunoki M: Scanning-tunneling-microscopy of the formation of carbon nanocaps on SiC(0 0 0 -1). Chem Phys Lett 2006, 423: 317. 10.1016/j.cplett.2006.03.029
Takagi D, Hibino H, Suzuki S, Kobayashi Y, Homma Y: Carbon Nanotube Growth from Semiconductor Nanoparticles. Nano Lett 2007, 7: 2272. 10.1021/nl0708011
Botti S, Asilyan CRL, Dominicis LD, Fabbri F, Orlanducci S, Fiori A: Carbon nanotubes grown by laser-annealing of SiC nano-particles. Chem Phys Lett 2004, 400: 264. 10.1016/j.cplett.2004.10.119
Botti S, Asilyan LS, Ciardi R, Fabbri F, Lortei S, Santoni A, Orlanducci S: Catalyst-free growth of carbon nanotubes by laser-annealing of amorphous SiC films. Chem Phys Lett 2001, 396: 1. 10.1016/j.cplett.2004.06.132
Uchino T, Bourdakos KN, de Groot CH, Ashburn P, Kiziroglou ME, Dilliway GD, Smith DC: Catalyst free low temperature, direct growth of carbon nanotubes. Proceedings of 2005 5th IEEE Conference on Nanotechnology 2005, 5: 1.
Uchino T, Bourdakos KN, de Groot CH, Ashburn P, Kiziroglou ME, Dilliway GD, Smith DC: Metal catalyst-free low-temperature carbon nanotube growth on SiGe islands. Appl Phys Lett 2005, 86: 233110. 10.1063/1.1946191
Liu H, Takagi D, Ohno H, Chiashi S, Chokan T, Homma Y: Growth of Single-Walled Carbon Nanotubes from Ceramic Particles by Alcohol Chemical Vapor Deposition. Appl Phys Express 2008, 1: 014001. 10.1143/APEX.1.014001
Steiner SA, Baumann TF, Bayer BC, Blume R, Worsley MA, MoberlyChan WJ, Shaw EJ, Schlogl R, Hart AJ, Hofmann S, Wardle BL: Nanoscale Zirconia as a Nonmetallic Catalyst for Graphitization of Carbon and Growth of Single- and Multiwall Carbon Nanotubes. J Am Chem Soc 2009, 131: 12144. 10.1021/ja902913r
Bystrzejewski M, Bachmatiuk A, Thomas J, Ayala P, Huebers H-W, Gemming T, Borowiak-Palen E, Pichler T, Kalenczuk RJ, Büchner B, Rümmeli MH: Boron doped carbon nanotubes via ceramic catalysts. Phys Stat Sol RRL 2009, 3: 193. 10.1002/pssr.200903088
Bachmatiuk A, Bystrzejewski M, Schäffel F, Ayala P, Wolff U, Mickel C, Gemming T, Pichler T, Borowiak-Palen E, Klingeler R, Huebers H-W, Ulbrich M, Knupfer M, Haberer D, Büchner B, Rümmeli MH: Carbon nanotube synthesis via ceramic catalysts. Phys Stat Sol B 2009, 246: 2486. 10.1002/pssb.200982308
Liu B, Ren W, Gao L, Li S, Pei S, Liu C, Jiang C, Cheng H-M: Metal-Catalyst-Free Growth of Single-Walled Carbon Nanotubes. J Am Chem Soc 2009, 131: 2082. 10.1021/ja8093907
Huang S, Cai Q, Chen J, Qian Y, Zhang L: J Am Chem Soc. 2009, 131: 2094. 10.1021/ja809635s
Bachmatiuk A, Börrnert F, Grobosch M, Schäffel F, Wolff U, Scott A, Zaka M, Warner JH, Klingeler R, Knupfer M, Büchner B, Rümmeli MH: Investigating the graphitization mechanism of SiO2 nanoparticles in chemical vapor deposition. ACS Nano 2009, 3: 4098. 10.1021/nn9009278
Bachmatiuk A, Börrnert F, Schäffel F, Zaka M, Simha-Martynkowa G, Placha D, Schönfelder R, Costa PMFJ, Ioannides N, Warner JH, Klingeler R, Büchner B, Rümmeli MH: The formation of stacked-cup carbon nanotubes using chemical vapor deposition from ethanol over silica. Carbon 2010, 48: 3175. 10.1016/j.carbon.2010.04.055
Schneider JJ, Maksimova NI, Engstler J, Joshi R, Schierholz R, Feile R: Catalyst free growth of a carbon nanotube-alumina composite structure. Inorg Chim Acta 2008, 361(6):1770. 10.1016/j.ica.2006.10.025
Rümmeli MH, Kramberger C, Grüneis A, Ayala P, Gemming T, Büchner B, Pichler T: On the graphitization nature of oxides for the formation of carbon nanostructures. Chem Mater 2007, 19: 4105.
Haruta M: Size- and support-dependency in the catalysis of gold. Catal Today 1997, 36: 153. 10.1016/S0920-5861(96)00208-8
Rümmeli MH, Schäffel F, Kramberger C, Gemming T, Bachmatiuk A, Kalenczuk RJ, Rellinghaus B, Büchner B, Pichler T: Oxide-driven carbon nanotube growth in supported catalyst CVD. J Am Chem Soc 2007, 129: 15772.
Rümmeli MH, Schäffel F, Bachmatiuk A, Adebimpe D, Trotter G, Börrnert F, Scott A, Coric E, Sparing M, Rellinghaus B, McCormick PG, Cuniberti G, Knupfer M, Schultz L, Büchner B: Investigating the outskirts of Fe and Co catalyst particles in alumina-supported catalytic CVD carbon nanotube growth. ACS Nano 2010, 4(2):1146.
Yoshida H, Yoshida H, Takeda S, Uchiyama T, Kohno H, Homma Y: Atomic-Scale In-situ Observation of Carbon Nanotube Growth from Solid State Iron Carbide Nanoparticles. Nano Lett 2008, 8: 2082. 10.1021/nl080452q
Schäffel F, Täschner C, Rümmeli MH, Neu V, Wolff U, Queitsch U, Pohl D, Kaltofen R, Leonhardt A, Rellinghaus B, Büchner B, Schultz L: Carbon nanotubes terminated with hard magnetic FePt nanomagnets. Appl Phys Lett 2009, 94: 193107.
Vander Wal RL, Tichich TM, Curtis VE: Substrate-support interactions in metal-catalyzed carbon nanofiber growth. Carbon 39: 2277. 10.1016/S0008-6223(01)00047-1
Bacon R, Bowman JC: Production and properties of graphite whiskers. Bull Am Phys Soc 1957, 2: 131.
Takagi D, Kobayashi Y, Homma Y: Carbon Nanotube Growth from Diamond. J Am Chem Soc 2009, 131: 6922. 10.1021/ja901295j
Rao F, Li T, Wang Y: Growth of "all-carbon" single-walled carbon nanotubes from diamonds and fullerenes. Carbon 47: 353.
Yu X, Zhang J, Choi W, Choi J-Y, Kim JM, Gan L, Liu Z: Cap Formation Engineering: From Opened C60 to Single-Walled Carbon Nanotubes. Nano Lett 2010, 10: 3343. 10.1021/nl1010178
Yao Y, Feng C, Zhang J, Liu Z: "Cloning" of Single-Walled Carbon Nanotubes via Open-End Growth Mechanism. Nano Lett 2009, 9: 1673. 10.1021/nl900207v
Lin J-H, Chen C-S, Rümmeli MH, Zeng Z-Y: Self-assembly formation of multi-walled carbon nanotubes on gold surfaces. Nanoscale 2010, 2: 2835. 10.1039/c0nr00256a
Lin JH, Chen CS, Rümmeli MH, Bachmatiuk A, Zeng ZY, Ma HL, Büchner B, Chen HW: Growth of Carbon Nanotubes Catalyzed by Defect-Rich Graphite Surfaces. Chem Mater 2010.
Reilly PTA, Whitten WB: The role of free radical condensates in the production of carbon nanotubes during the hydrocarbon CVD process. Carbon 2006, 44: 1653. 10.1016/j.carbon.2006.01.018
Rümmeli MH, Bachmatiuk A, Scott A, Börrnert F, Warner JH, Hoffman V, Lin J-H, Cuniberti G, Büchner B: Direct low-temperature nanographene CVD synthesis over a dielectric insulator. ACS Nano 2010, 4: 4206.
Zhu MY, Wang JJ, Holloway BC, Outlaw RA, Zhao X, Hou K, Shutthanandan V, Manos DM: A mechanism for carbon nanosheet formation. Carbon 45: 2229. 10.1016/j.carbon.2007.06.017
Wang JJ: Free-standing subnanometer graphite sheets. Appl Phys Lett 2004, 85: 1265. 10.1063/1.1782253
Dato A, Radmilovic V, Lee Z, Phillips J, Frenklach M: Substrate-Free Gas-Phase Synthesis of Graphene Sheets. Nano Lett 2008, 8: 2012. 10.1021/nl8011566
MacKenzie KJ, See CH, Dunens OM, Harris AT: Do single-walled carbon nanotubes occur naturally? Nat Nanotechnol 2008, 3: 310. 10.1038/nnano.2008.139
Fries M, Steel A: Graphite Whiskers in CV3 Meteorites. Science 2008, 320: 91. 10.1126/science.1153578
Nuth JA, Johnson NM, Manning S: A Self-Perpetuating Catalyst for the Production of Complex Organic Molecules in Protostellar Nebulae. Astrophys J Lett 2008, 673: L225. 10.1086/528741
Nuth JA, Johnson NM, Manning S: A Self-Perpetuating Catalyst for the Production of Complex OrganicMolecules in Protostellar Nebulae. In IAU Symp. 251, Organic Matter in Space. Edited by: Kwok S, Sandford S. New York: Cambridge University Press; 2008:403.
Nuth JA, Kimura K, Lucas C, Ferguson F, Johnson NM: The formation of graphite whiskers in the primitive solar nebula. Astrophys J Lett 2010, 710: L98. 10.1088/2041-8205/710/1/L98
MHR thanks the EU (ECEMP) and the Freistaat Sachsen, AB and FS the Alexander von Humboldt Foundation and the BMBF, FB the DFG (RU 1540/8-1), II the DAAD (A/07/80841) and CC the EU (CARBIO, Contract MRTN-CT-2006-035616). GC acknowledges support from the South Korean Ministry of Education, Science, and Technology Program, Project WCU ITCE No. R31-2008-000-10100-0.
The authors declare that they have no competing interests.
MHR designed the manuscript layout. MHR, AB, FB, FS, II, KC, GS-M, DP, EB-P, GC and BB participated in some of the studies and participated in the drafting of the manuscript. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Rümmeli, M.H., Bachmatiuk, A., Börrnert, F. et al. Synthesis of carbon nanotubes with and without catalyst particles. Nanoscale Res Lett 6, 303 (2011). https://doi.org/10.1186/1556-276X-6-303
- Catalyst Particle
- SiO2 Nanoparticles
- Filamentous Carbon
- Magnesium Borate