Synthesis of Single-Walled Carbon Nanotubes: Effects of Active Metals, Catalyst Supports, and Metal Loading Percentage

Liu, Wei-Wen; Aziz, Azizan; Chai, Siang-Piao; Mohamed, Abdul Rahman; Hashim, U.

doi:https://doi.org/10.1155/2013/592464

Journal of Nanomaterials

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Abstract Introduction Results and Discussion Conclusion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2013 | Article ID 592464 | https://doi.org/10.1155/2013/592464

Synthesis of Single-Walled Carbon Nanotubes: Effects of Active Metals, Catalyst Supports, and Metal Loading Percentage

Wei-Wen Liu,^1,2Azizan Aziz,²Siang-Piao Chai,³Abdul Rahman Mohamed,⁴and U. Hashim¹

Academic Editor: Shiren Wang

Received12 Apr 2013

Revised05 Jun 2013

Accepted13 Jun 2013

Published27 Jun 2013

Abstract

The effects of active metals, catalyst supports, and metal loading percentage on the formation of single-walled carbon nanotubes (SWNTs) were studied. In particular, iron, cobalt, and nickel were investigated for SWNTs synthesis. Iron was found to grow better-quality SWNTs compared to cobalt and nickel. To study the effect of catalyst supports, magnesium oxide, silicon oxide, and aluminium oxide were chosen for iron. Among the studied supports, MgO was identified to be a suitable support for iron as it produced SWNTs with better graphitisation determined by Raman analysis. Increasing the iron loading decreased the quality of SWNTs due to extensive agglomeration of the iron particles. Thus, lower metal loading percentage is preferred to grow better-quality SWNTs with uniform diameters.

1. Introduction

Besides laser evaporation and electric arc discharge methods, the catalytic chemical vapor deposition (CVD) is a very efficient method to synthesize single-walled carbon nanotubes (SWNTs) on a large scale but a low cost [1–3]. It is well known that the catalyst is indispensable for the growth of SWNTs in CVD process. A variety of metal catalysts such as Au, Ag, Pt, Pd, Mn, Mo, Cu, Rh, Zn, Cr, Ru, Mg, and Al have been used for the production of SWNTs [4–11]. However, Fe, Co, Ni, and their alloys are the most of the widely used transition metal catalysts for SWNT production [12–14]. So far, various substances have been tested as supports of catalytically active metals, for instance, zeolites [15, 16], SiO₂ [17], Al₂O₃ [18], CaCO₃ [19], and MgO [20]. The interactions between the support and active metal are greatly important in the synthesis of SWNTs because it can affect the quality of SWNTs. In addition, the dependency of structure upon property causes the structure control and large-scale production of SWNTs to become one of the crucial topics in carbon related scientific communities [21–25]. Clear understanding of underlying growth mechanisms is therefore of significant importance in promoting the development and innovations of SWNTs.

Thus, there is a need to investigate the effects of active metals, catalyst supports, and metal loading percentage on the production of SWNTs. Our previous study shows that Fe₃O₄/MgO was an effective catalyst for growing SWNTs [26–29]. We had also reported that the quality of SWNTs was affected by the types of carbon precursors used [27]. In this work, the effects of active metals such as Fe, Ni, and Co were chosen because they are believed to yield high quality of SWNTs, but we are unsure which active metals can synthesise the highest quality of SWNT when supported by MgO under our reaction conditions. It is because a minor change on the reaction parameters can influence the active metals’ performances. In the second study, the best performance active metal was supported by MgO, SiO₂, and Al₂O₃ to investigate the interaction between supports and active metal which can affect the yield of SWNTs. At last study, different metal loading percentages were set to examine the effect on the quality of SWNTs.

2. Experimental Procedures

2.1. Preparation of the Catalyst

The preparation method for Fe₃O₄ nanoparticles has been previously reported [29]. The molar ratios of Fe₃O₄ to MgO, NiO to MgO, and CoO to MgO were set at 1 : 9. Fe₃O₄/MgO, NiO/MgO, and CoO/MgO catalysts were prepared by dispersing MgO (99.99% trace metal basis: Aldrich) in distilled water and subsequently adding the required amount of Fe₃O₄ nanoparticles, Ni (NO₃)₂·6H₂O (99.999% trace metal basis: Aldrich) and Co (NO₃)₂·6H₂O (99.999% trace metal basis: Aldrich), respectively, into the MgO solution to get three different types of mixture solutions. For the preparation of Fe₃O₄/Al₂O₃ and Fe₃O₄/SiO₂ catalysts, the molar ratios of Fe₃O₄ to Al₂O₃ and Fe₃O₄ to SiO₂ were set at 1 : 9. The required amount of Fe₃O₄ nanoparticles was dispersed in distilled water and followed by adding Al₂O₃ (analytical reagents: Ajax) and SiO₂ nanopowder (analytical reagents: RdH), respectively, to form two different types of mixture solutions. To prepare different molar ratios of Fe₃O₄/MgO catalysts at 1.75 : 8.25, 2.5 : 7.5, and 3.25 : 6.75, the same procedure as above was used. All mixture solutions were then sonicated for 10 min, and water was removed by rotary evaporation. Finally, the dried catalyst was ground with a pestle and mortar to break the agglomerates into a very fine powder.

2.2. Synthesis of SWNTs

The synthesis of SWNTs was carried out at atmospheric pressure in a quartz tube placed vertically in a stainless-steel housing [26–29]. For the synthesis of SWNTs, 0.2 g of the catalyst was distributed in the centre of the reactor for each run. The reactor was heated in a tubular furnace to 900°C in a nitrogen atmosphere (99.999% purity) at a flow rate of 40 mL/min. Subsequently, high-purity methane (99.999% purity) was mixed with nitrogen at a ratio of 1 : 1 (v/v) before introducing the mixed gas into the reactor at a total flow rate of 80 mL/min. The reaction was kept under these conditions for 30 min. After the reaction, the furnace was cooled to room temperature in a nitrogen flow.

2.3. Characterization of SWNTs

The carbon samples, in black powder form, were collected from the quartz reactor for detail characterisation. The morphology of the SWNTs was investigated using transmission electron microscopy (TEM; Philips CM12) and scanning electron microscopy (SEM; Supra 35 VP). Raman spectrum measurements were conducted on the carbon samples using a Raman spectroscopy (inVia Renishaw) at a wavelength of 633 nm.

3. Results and Discussion

3.1. Effect of Fe₃O₄, NiO, and CoO Supported on MgO

The ability of Fe₃O₄/MgO, NiO/MgO, and CoO/MgO catalysts to produce SWNTs was investigated. The study was based on the ratio from Raman spectra of SWNTs produced over these catalysts. The ratio is commonly used as a measure of the quality of CNTs produced: a smaller ratio corresponds to a higher quality structure or fewer defects [30]. The ratios for samples produced by Fe₃O₄/MgO, NiO/MgO, and CoO/MgO catalysts were 0.11, 0.65, and 0.34, respectively, decreasing in the order of NiO/MgO > CoO/MgO > Fe₃O₄/MgO. A high ratio of 0.65 was obtained for the NiO/MgO catalyst, indicating that a low-quality structure was formed. The Fe₃O₄/MgO catalyst formed better-quality CNTs where ratio of 0.11 was obtained. Figure 1 shows the Raman spectra of the three different catalyst systems after reaction. The presence of the radial breathing mode (RBM) and G- and D-bands in the Raman spectra confirms the presence of SWNTs. The frequency of the RBM is inversely proportional to the diameter of the nanotube from which it arises. It has been found empirically that the diameter of the tube (/nm) can relate to the frequency of RBM by , where cm⁻¹, cm⁻¹, and = diameter of SWNTs in nanometer [31].

It is important to note the significant peaks at Raman shifts of 203 and 190 cm⁻¹, which correspond to the nanotube diameters of 1.22, 1.30, and 1.31 nm produced by the NiO/MgO, CoO/MgO, and Fe₃O₄/MgO catalysts, respectively. The nanotube samples were also characterised using transmission electron microscopy (TEM) and their results are shown in Figure 2. It can be observed that bundles of SWNTs with nearly uniform diameters were synthesised by Fe₃O₄/MgO, NiO/MgO, and CoO/MgO catalysts. Bundles that consist of more than 20 SWNTs were obtained from the Fe₃O₄/MgO catalyst. In addition to the SWNT bundles, MWNTs were also observed under TEM for the NiO/MgO catalyst but not for the Fe₃O₄/MgO and CoO/MgO catalysts.

(a)

(b)

(c)

To arrive at the understanding why the Fe₃O₄/MgO catalyst formed SWNTs with a lower ratio, we have to understand the carbon solubility for Fe, Ni, and Co. Moisala et al. [31] reported that the carbon solubilities for Fe, Co, and Ni are 20.2, 13.9, and 10.7%, respectively, at a given temperature. Fe has the highest carbon solubility as compared with Co and Ni. The higher carbon solubility of Fe influences CNT nucleation and growth in several ways: (i) increasing the carbon availability for CNT growth; (ii) creating a higher concentration driving force to accelerate the CNT formation rate; (iii) affecting nucleation of CNT caps; and (iv) determining the type of CNT grown [32]. By thermodynamic analysis, Kuznetsov et al. [33] reported that the morphology of nanotubes is a function of two parameters: the diameter of the catalyst particle and the carbon supersaturation ratio. When the supersaturation value is high, carbon caps can be formed easily from the multiple carbon nuclei on the same particle surface. Due to the van der Waals forces, the SWNTs may be reoriented to form SWNT bundles. Therefore, Fe tends to have a higher carbon supersaturation ratio compared with Co and Ni because of its higher carbon solubility of Fe, which promotes the nucleation and growth of SWNTs and also explains why broad bundles of SWNTs with a more highly graphitised structure were formed on the Fe₃O₄/MgO catalyst.

3.2. Effect of Al₂O₃, SiO₂, and MgO Supports

Figure 3 shows the Raman spectra for samples produced by Fe₃O₄ supported on SiO₂, Al₂O₃, and MgO. The ratio for samples produced by Fe₃O₄ supported on SiO₂, Al₂O₃, and MgO were 0.34, 0.29, and 0.11, respectively. RBM in the range of 100–350 cm⁻¹ are attributed to the presence of SWNTs [34]. In Figure 3, RBM peaks were observed for all three catalysts investigated, revealing the formation of SWNTs. The intensity of RBM peaks decreased in the following order of Fe₃O₄/MgO > Fe₃O₄/SiO₂ > Fe₃O₄/Al₂O₃, whereas the ratio decreased in the order of Fe₃O₄/SiO₂ > Fe₃O₄/Al₂O₃ > Fe₃O₄/MgO. In other words, compared with SiO₂ and Al₂O₃, MgO-supported Fe₃O₄ represents the most suitable combination to produce SWNTs, considering that the highest intensity of RBM peaks and the lowest ratio were observed. This is in good agreement with the finding reported by Ago et al. [35] and Jin et al. [36] that high quality of SWNTs were synthesised by iron supported on MgO catalyst.

The diameter of SWNTs obtained was in the range of 1.09–2.40 nm. In this work, CNTs with diameters greater than 2.48 nm were considered large diameter CNTs, whereas CNTs with diameters of 2.48 nm or less were defined as small-diameter CNTs. Scanning electron microscopy (SEM) images for all samples are shown in Figure 4. CNTs with diameters greater than 2.48 nm were produced when SiO₂ was used as a catalyst support (Figure 4(a)), whereas CNTs with small diameters were formed when Al₂O₃ and MgO were used (Figures 4(b) and 4(c)). The diameters of CNTs synthesised by Fe₃O₄ supported on Al₂O₃ and MgO were measured using TEM, and the results are shown in Figure 5. The diameter ranges were 1.22–1.46 nm and 1.09–2.40 nm for CNTs produced by Al₂O₃ and MgO when used as catalyst supports, respectively. The diameters were almost uniform, and the CNTs attached to one another in a bundle form (Figure 5). The bundle produced by the MgO-supported catalyst consisted of more SWNTs compared with that produced by Al₂O₃ as the catalyst support (Figure 5). The TEM observations show that SWNTs synthesised by MgO used as the support were of high quality, which is consistent with the Raman analysis.

(a)

(b)

(c)

(a)

(b)

To understand why MgO was a superior support, we considered the interaction between the metal oxide nanoparticle and its support. The formation of the highest-quality SWNTs by the Fe₃O₄/MgO catalyst could be attributed to the strong metal interaction between the Fe₃O₄ nanoparticles and MgO [37, 38]. This strong interaction restricted the mobility of Fe₃O₄ nanoparticles during CVD, thus preventing the extensive agglomeration of Fe₃O₄ nanoparticles at high temperatures to form larger-sized clusters, leading to good dispersion of Fe₃O₄ [39]. This strong interaction can be explained in terms of Lewis acid/base interactions between metal oxide supports and metal catalyst nanoparticles. A Lewis base is a species that acts as an electron pair donor, whereas a Lewis acid is a species that acts as an electron pair acceptor [39]. In this case, the metal oxide support (MgO) acts as a Lewis base and donates electrons through metal catalyst nanoparticles (Fe₃O₄) to methane [39]. The metal catalyst nanoparticles play the role of a conduit for transferring negative charge from the metal oxide support to methane. Generally, simultaneous back-donation from methane also takes place that is, methane acts as a Lewis base, whereas MgO acts as a Lewis acid. The electronic structure of methane is then changed in such a way that decomposition of the methane molecule takes place.

The surface basicity was reported to decrease in the following order: MgO > Al₂O₃ > SiO₂ [40]. Thus, MgO represents the best electron donor compared with Al₂O₃ and SiO₂. As a result, the interaction between Fe₃O₄ and MgO was stronger than the interactions between Fe₃O₄ and Al₂O₃ and between Fe₃O₄ and SiO₂ [40]. With the strong interaction between the Fe₃O₄ and MgO, Fe₃O₄ particles are thought to be well dispersed and promote the formation of SWNTs. This explains the reason of intensity of the RBM peaks for the samples produced by MgO used as a catalyst support was the highest and the ratio was the lowest compared with the samples formed by SiO₂ and Al₂O₃. The second highest intensity of RBM peaks was observed for samples formed by SiO₂ used as the catalyst support compared with the samples produced by Al₂O₃ used as the catalyst support. However, a higher ratio was observed in the Raman spectra of the sample produced by using an SiO₂ catalyst support than that formed when using an Al₂O₃ catalyst support. This indicates that more defective structures were formed in the samples due to the fact that SiO₂ is a less active support compared with alumina [41, 42]. Because Al₂O₃ is an amphoteric material having the characteristics of both an acid and a base, it may take part in the strong interaction. Therefore, Fe₃O₄ particles had a better dispersion on the Al₂O₃ compared with SiO₂ due to this strong interaction and formed a higher degree of CNT graphitisation.

3.3. Effect of Fe₃O₄ Loading

In this study, the molar ratios of Fe to MgO were varied at 1 : 9, 1.75 : 8.25, 2.5 : 7.5, and 3.25 : 6.75, which were denoted as (Fe₃O₄)₁(MgO)₉, (Fe₃O₄)_1.75(MgO)_8.25, (Fe₃O₄)_2.5(MgO)_7.5, and (Fe₃O₄)_3.25(MgO)_6.75, respectively. The CVD conducted using a molar ratio of 1 : 9 produced the lowest ratio, that is, 0.11. The ratios of samples were found to increase from 0.11 to 0.46 as the Fe₃O₄ loading increased from 1 to 3.25.

The Raman spectra shown in Figure 6 show the presence of RBM peaks, indicating the presence of SWNTs. The intensity of RBM peaks decreased in the following order for Fe₃O₄ loading: 1 > 1.75 > 2.5 > 3.25. The ratio was found to decrease in the following order: 3.25 > 2.5 > 1.75 > 1. In contrast, the highest intensity of RBM peak and the lowest ratio were observed for SWNTs produced by a catalyst with a molar ratio of 1 : 9.

The SEM images, shown in Figures 7(a) and 7(b), revealed the presence of narrow-diameter CNTs from (Fe₃O₄)₁(MgO)₉ and (Fe₃O₄)_1.75(MgO)_8.25 catalysts. The narrow CNTs grew over the entire catalyst surface with almost uniform diameters. However, large-diameter CNTs were observed in the samples formed by the (Fe₃O₄)_2.5(MgO)_7.5 and (Fe₃O₄)_3.25(MgO)_6.75 catalysts. The structures of large CNTs were poor and had inconsistent diameters, which can be seen in Figures 7(c) and 7(d).

(a)

(b)

(c)

(d)

To measure the diameters of narrow CNTs, samples produced by the (Fe₃O₄)₁(MgO)₉ and (Fe₃O₄)_1.75(MgO)_8.25 catalysts were characterised by TEM. The measured diameter was in the range of 1.16–2.10 nm and 1.10–1.85 nm for SWNTs synthesised by (Fe₃O₄)₁(MgO)₉ and (Fe₃O₄)_1.75(MgO)_8.25 catalyst, respectively. Figure 8 clearly shows SWNTs in a bundle form produced by the (Fe₃O₄)₁(MgO)₉ and (Fe₃O₄)_1.75(MgO)_8.25 catalysts. Under TEM observation, the diameter of these SWNTs was almost uniform and in agreement with the SEM observations (Figures 7(a) and 7(b)). Moreover, the SWNTs bundles possessed a high degree of graphitization, which is consistent with the Raman results (Figure 6).

(a)

(b)

From these results, it is clear that there is an optimum Fe₃O₄ loading that leads to the formation of SWNTs of the desired quality. When increasing the Fe₃O₄ loading by more than 1.75, the ratio also increased significantly, and large CNTs were clearly observed in the samples (Figures 7(c) and 7(d)). Increasing the Fe₃O₄ content is beneficial only if it enhances the available active sites for CNT growth, rather than increasing the nanoparticle sizes [43–47]. It is well known that the diameters of CNTs are correlated with active metal nanoparticles sizes [32, 40, 48–50]. Therefore, the narrow CNTs in this work were likely produced by small Fe₃O₄ nanoparticles, and the large CNTs by large Fe₃O₄ nanoparticles. Therefore, the quality of CNTs decreased with an increase in Fe₃O₄ loading.

The average size of Fe₃O₄ nanoparticles for (Fe₃O₄)₁(MgO)₉ catalyst was 10.33 nm as reported in our previous work [42]. In this work, the size of catalyst nanoparticles for the (Fe₃O₄)₁(MgO)₉ catalyst was much smaller than the size of catalyst nanoparticles for (Fe₃O₄)_1.75(MgO)_8.25, (Fe₃O₄)_2.5(MgO)_7.5, and (Fe₃O₄)_3.25(MgO)_6.75, as observed in Figure 7. The large nanoparticle catalysts were formed for the high Fe₃O₄-loaded: (Fe₃O₄)_1.75(MgO)_8.25, (Fe₃O₄)_2.5(MgO)_7.5, and (Fe₃O₄)_3.25(MgO)_6.75 catalysts due to the sintering of the Fe₃O₄ nanoparticles during reaction at high temperatures (i.e., 900°C) [33]. Sintering is a thermally activated process that involves the diffusion of atoms [51]. Together with the higher concentration of iron, there would be a significantly higher degree of sintering of iron nanoparticles, causing large nanoparticles to form. However, it is believed that the degree of sintering of iron nanoparticles for (Fe₃O₄)₁(MgO)₉ was low compared with those of the (Fe₃O₄)_1.75(MgO)_8.25, (Fe₃O₄)_2.5(MgO)_7.5, and (Fe₃O₄)_3.25(MgO)_6.75 catalysts. As a result, the sizes of iron nanoparticles are small for a molar ratio of 1 : 9.

4. Conclusion

Our experimental findings show that among the types of active metals and supports investigated, Fe₃O₄ supported on MgO is the most suitable catalyst. High-quality SWNTs were synthesised using an Fe₃O₄/MgO catalyst with a molar ratio of 1 : 9. It is believed that iron has a higher carbon solubility than either cobalt or nickel, which helps to promote the formation of SWNTs. In addition, the interaction between Fe₃O₄ and MgO is strong, which prevents agglomeration of Fe₃O₄ and produces CNTs with a high degree of graphitisation. Using a low molar ratio of Fe₃O₄ to MgO could reduce the agglomeration of Fe₃O₄ nanoparticles. Therefore, the most suitable Fe₃O₄ loading found was at an Fe₃O₄ to MgO molar ratio of 1 : 9.

Acknowledgments

The authors gratefully acknowledge the financial support provided by the Universiti Sains Malaysia under Fundamental Research Grant Scheme (FRGS) (Project A/C no. 6071002), the Research University Grant (RU) (Project A/C no. 814004), Skim Penyelidikan Siswazah Universiti Penyelidikan (USM-RU-PRGS) (Project A/C no. 8042015), and Universiti Sains Malaysia Fellowship.

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Copyright © 2013 Wei-Wen Liu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Journal of Nanomaterials

Synthesis of Single-Walled Carbon Nanotubes: Effects of Active Metals, Catalyst Supports, and Metal Loading Percentage

Abstract

1. Introduction

2. Experimental Procedures

2.1. Preparation of the Catalyst

2.2. Synthesis of SWNTs

2.3. Characterization of SWNTs

3. Results and Discussion

3.1. Effect of Fe3O4, NiO, and CoO Supported on MgO

3.2. Effect of Al2O3, SiO2, and MgO Supports

3.3. Effect of Fe3O4 Loading

4. Conclusion

Acknowledgments

References

Copyright

3.1. Effect of Fe₃O₄, NiO, and CoO Supported on MgO

3.2. Effect of Al₂O₃, SiO₂, and MgO Supports

3.3. Effect of Fe₃O₄ Loading