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ISRN Materials Science
Volume 2013 (2013), Article ID 732974, 4 pages
Synthesis of Co Filled Carbon Nanotubes by In Situ Reduction of CoCl2 Filled Nanotubes by NaBH4
Amity Institute of Nanotechnology, Amity University, Sector 125, Noida, 201313 UP, India
Received 13 May 2013; Accepted 13 June 2013
Academic Editors: V. Baranauskas and S. X. Dou
Copyright © 2013 J. Mittal. 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.
An alternative process of filling the multiwall nanotubes (MWCNTs) with cobalt metal was developed. Empty core of nanotubes was first filled with CoCl2 by stirring with CoCl2 and alcohol at room temperature for six hours. CoCl2 filling inside MWCNTs was then converted into Co after treating with NaBH4 at room temperature. High resolution transmission electron microscope (HRTEM) studies showed the filling of the CoCl2 and Co inside the nanotubes before and after the treatment. EDX studies show the nonexistence of chlorine after the reduction with NaBH4. Amount of filling was also reduced after the treatment. Paper describes the possible mechanism of filling CoCl2 inside nanotube and its reduction by NaBH4.
Exceptional properties of carbon nanotubes, like high strength, discrete electronic states, and so forth, make them highly suitable for the applications in nanodevices. They are the most appropriate material for using in devices like AFM probes , FE transistors [2, 3] display devices [4–6], and so forth. Filling of carbon nanotubes with materials enhances their physical and chemical properties and their potential applications in different areas [7–9]. They show interesting physical and structural properties which are different than their parent materials [7, 10].
Magnetic metal nanoparticles (such as Fe, Co, and Ni) have applications such as high-density magnetic data storage, magnetic separation of biomolecules, and treatment of cancer [11, 12]. However, the poor oxidation resistance of the metal nanoparticles is a great hindrance for their applications. Encapsulation of nanoparticles in carbon nanotubes may be highly useful with the combination of properties of magnetic nanoparticles and carbon nanotubes [13–16]. Ferromagnetic metals filled carbon nanotubes have significant potential in data storage technology . Additionally, the walls of carbon nanotubes provide an effective shelter against oxidation of magnetic nanoparticles and thus ensure a long-term stability of the ferromagnetic core .
Various methods are employed for the filling of carbon nanotubes, such as arc discharge [18, 19], high-temperature heat treatment , capillary induced , ion-beam sputtering , and chemical vapor deposition (CVD) [23, 24]. Although arc discharge technique is a better method, low yield is a problem for commercial applications. CVD method is a simple and low cost method and can produce filled carbon nanotubes in large quantities. However, all these methods are the in situ synthesis of metal filled nanotubes. There are very few studies for the filling the CNTs using after their preparation [9, 10]. The present paper describes an easy method of the filling of the carbon nanotubes using first CoCl2 and then reducing the CoCl2 into Co using NaBH4.
2. Materials and Methods
MWCNTs obtained from ASI, open from both ends, having a diameter in the range from 150 to 200 nm, were taken in a flask and mixed with CoCl2 in alcohol in equal molar ratio. The mixture was stirred for 6 hours at room temperature in air. After stirring, the sample was washed with alcohol for the removal of unreacted CoCl2. CoCl2 filled MWCNTs were then mixed with NaBH4 in alcohol, and the mixture was cooled down to 273 K. The reaction between CoCl2 filled MWCNTs and NaBH4 was carried out in inert atmosphere of argon. The mixture was then stirred for 6 hours. Once the treatment time were over, nanotubes were taken out from flask, washed with alcohol, and characterized.
Structural investigation of the products was done using high resolution transmission electron microscope (HRTEM) operating at 150 KVa with a point resolution of 3 Å. Contrast was enhanced by adding an 8 nm large aperture in the back focal plane on the objective lens. Electron dispersive X-ray spectroscopy was used to characterize the elemental analysis.
3. Results and Discussion
3.1. CoCl2 Filled Multiwalled Nanotubes
HRTEM micrographs in Figures 1(a) and 1(b) demonstrate two MWCNTs after stirring with CoCl2. Some part of the central hole of nanotubes, shown between two lines, is observed to be darker than the nanotube walls. This dark material is the filling inside the empty core of the nanotubes. Filling appears darker than the nanotubes walls whereas the empty hole appears lighter than the walls. Core of nanotube is observed to be filled at few places whereas other places are seen empty. Material is not filled throughout the nanotube hole. Filling is dense in Figure 1(b) whereas it is slightly transparent in Figure 1(a). This transparency may be due to the entrance of liquid in the nanotubes.
High magnification study in Figure 2(a) shows that some part of the filling is dense, and there is some crystalline nature in the filled material. The filling covers the entire width of the hole. Graphene layers of nanotube walls remain intact. There is no effect of the treatment on the nanotube walls.
Figure 2(b) shows EDX study of the filled material in Figure 2(a). Analysis demonstrates the presence of Cu, Co, and Cl in the filling. Since Cu grids are used for the study, observed Cu is due to the grid. Existence of Co and Cl indicates the presence of CoCl2.
3.2. Co Filled Multiwalled Nanotubes
Figure 3(a) shows a CoCl2 filled nanotube after treatment with NaBH4. A quadrilateral size particle of dimensions 100 × 60 nm is observed inside the nanotube. Nanoparticle covers the width of the nanotube. However, a slight gap appeared on the both sides between the nanotube wall and nanoparticles. This gap is not visible in the CoCl2 filled nanotubes (Figure 2(a)).
EDX study in the Figure 3(b) shows the presence of Co. No existence of Cl is observed in the filling. Reduction in size shows the removal of chlorine from the filling CoCl2. The nanoparticle is not as dense as the CoCl2. Some part is dense whereas the other part is hollow which may be due to the removal of Cl from the inside of crystalline CoCl2.
3.3. Mechanism of the Filling of CoCl2 and Reduction with NaBH4
Illustration in Figure 4 depicts the complete process of filling Co metal in multiwalled nanotube. Step 1 of the process is the stirring of nanotubes with CoCl2 in alcohol at room temperature in air for six hours. Since the nanotubes used are already open, CoCl2 along with alcohol enters in the empty hole of the nanotubes due to the capillary effect. This leads to the formation of CoCl2 filled MWCNTs (CoCl2@MWNTs), as shown by the following reaction: In the second step, CoCl2 MWNTs are treated with NaBH4 in ethyl alcohol at 273 K in argon atmosphere. This treatment converts CoCl2@MWCNTs into Co@MWCNTs with NaBH4, and CoCl2 get reduced to the Co, as shown in the following reaction: NaBH4 is a reducing agent and better known for the reduction of the aldehydes and acids in the organic chemistry. Besides these, it is also used for reducing metal chlorides into metals [25, 26]. Absence of chlorine in the EDX analysis of Co metal in Figure 3 indicates the reduction of CoCl2. NaBH4 may also form the CoB2 during the reduction , as observed in the earlier studies where water was used as a solvent. However, EDX analyses of Co metal in Figure 3 show the nonexistence of boron and oxygen. This shows that the conditions of the reaction (2) are not suitable for forming the CoB2 or Co2O3 and lead to the formation of pure Co metal inside the nanotube.
CoCl2 was successfully filled inside the multiwalled nanotubes after stirring both in alcohol for six hours. CoCl2 inside the nanotube is converted into Co by NaBH4 using alcohol as a solvent. Absence of chlorine, boron, and oxygen in the EDX study shows the formation of pure Co inside the nanotubes.
The author is thankful for Dr. A. K. Chauhan, founder president, Amity University, Dr. R. P. Singh, Advisor, and Tinku Basu, Head, Amity Institute of Nanotechnology, Amity University, for their help in publishing this work.
- H. Dai, J. H. Hafner, A. G. Rinzler, D. T. Colbert, and R. E. Smalley, “Nanotubes as nanoprobes in scanning probe microscopy,” Nature, vol. 384, no. 6605, pp. 147–150, 1996.
- S. J. Tans, A. R. M. Verschueren, and C. Dekker, “Room-temperature transistor based on a single carbon nanotube,” Nature, vol. 393, no. 6680, pp. 49–52, 1998.
- P. G. Collins, A. Zettl, H. Bando, A. Thess, and R. E. Smalley, “Nanotube nanodevice,” Science, vol. 278, no. 5335, pp. 100–102, 1997.
- W. A. De Heer, A. Châtelain, and D. Ugarte, “A carbon nanotube field-emission electron source,” Science, vol. 270, no. 5239, pp. 1179–1180, 1995.
- S. Fan, M. G. Chapline, N. R. Franklin, T. W. Tombler, A. M. Cassell, and H. Dai, “Self-oriented regular arrays of carbon nanotubes and their field emission properties,” Science, vol. 283, no. 5401, pp. 512–514, 1999.
- M. A. Burns, B. N. Johnson, S. N. Brahmasandra et al., “An integrated nanoliter DNA analysis device,” Science, vol. 282, no. 5388, pp. 484–487, 1998.
- M. Monthioux, “Filling single-wall carbon nanotubes,” Carbon, vol. 40, no. 10, pp. 1809–1823, 2002.
- J. Mittal and K. L. Lin, “Connecting carbon nanotubes using Sn,” Journal of Nanoscience and Nanotechnology, vol. 13, no. 1, pp. 1–7, 2013.
- G. Lota, E. Frackowiak, J. Mittal, and M. Monthioux, “High performance supercapacitor from chromium oxide-nanotubes based electrodes,” Chemical Physics Letters, vol. 434, no. 1–3, pp. 73–77, 2007.
- J. Mittal, M. Monthioux, H. Allouche, and O. Stephan, “Room temperature filling of single-wall carbon nanotubes with chromium oxide in open air,” Chemical Physics Letters, vol. 339, no. 5-6, pp. 311–318, 2001.
- U. Wiedwald and P. Ziemann, “Preparation, properties and applications of magnetic nanoparticles,” Beilstein Journal of Nanotechnology, vol. 1, pp. 21–23, 2010.
- D. Bahadur, J. Giri, B. B. Nayak et al., “Processing, properties and some novel applications of magnetic nanoparticles,” Pramana, vol. 65, no. 4, pp. 663–679, 2005.
- Y.-J. Kang, J. Choi, C.-Y. Moon, and K. J. Chang, “Electronic and magnetic properties of single-wall carbon nanotubes filled with iron atoms,” Physical Review B, vol. 71, no. 11, Article ID 115441, 2005.
- S. Karmakar, P. K. Tyagi, D. S. Misra, and S. M. Sharma, “Pressure-induced phase transitions in cobalt-filled multiwalled carbon nanotubes,” Physical Review B, vol. 73, no. 18, Article ID 184119, 2006.
- S. Karmakar, S. M. Sharma, M. D. Mukadam, S. M. Yusuf, and A. K. Sood, “Magnetic behavior of iron-filled multiwalled carbon nanotubes,” Journal of Applied Physics, vol. 97, no. 5, Article ID 054306, 2005.
- S. Karmakar, S. M. Sharma, P. V. Teredesai, and A. K. Sood, “Pressure-induced phase transitions in iron-filled carbon nanotubes: X-ray diffraction studies,” Physical Review B, vol. 69, no. 16, Article ID 165414, p. 1, 2004.
- A. Leonhardt, M. Ritschel, R. Kozhuharova et al., “Synthesis and properties of filled carbon nanotubes,” Diamond and Related Materials, vol. 12, no. 3-7, pp. 790–793, 2003.
- C. Guerret-Piécourt, Y. Le Bouar, A. Loiseau, and H. Pascard, “Relation between metal electronic structure and morphology of metal compounds inside carbon nanotubes,” Nature, vol. 372, no. 6508, pp. 761–765, 1994.
- Y. Yosida, S. Shida, T. Ohsuna, and N. Shiraga, “Synthesis, identification, and growth mechanism of Fe, Ni, and Co crystals encapsulated in multiwalled carbon nanocages,” Journal of Applied Physics, vol. 76, no. 8, pp. 4533–4539, 1994.
- P. M. Ajayan and S. Lijima, “Capillarity-induced filling of carbon nanotubes,” Nature, vol. 361, no. 6410, pp. 333–334, 1993.
- P. J. F. Harris and S. C. Tsang, “A simple technique for the synthesis of filled carbon nanoparticles,” Chemical Physics Letters, vol. 293, no. 1-2, pp. 53–58, 1998.
- T. Hayashi, S. Hirono, M. Tomita, and S. Umemura, “Magnetic thin films of cobalt nanocrystals encapsulated in graphite- like carbon,” Nature, vol. 381, no. 6585, pp. 772–774, 1996.
- P. E. Nolan, D. C. Lynch, and A. H. Cutler, “Catalytic disproportionation of CO in the absence of hydrogen: encapsulating shell carbon formation,” Carbon, vol. 32, no. 3, pp. 477–483, 1994.
- Z. J. Liu, Z. Y. Yuan, W. Zhou, Z. Xu, and L. M. Peng, “Controlled synthesis of carbon-encapsulated Co nanoparticles by CVD,” Advanced Materials, vol. 13, no. 21, pp. 248–251, 2001.
- G. N. Glavee, K. J. Klabunde, C. M. Sorensen, and G. C. Hadjapanayis, “Borohydride reductions of metal ions. A new understanding of the chemistry leading to nanoscale particles of metals, borides, and metal borates,” Langmuir, vol. 8, no. 3, pp. 771–773, 1992.
- C. A. Brown and V. K. Ahuja, “Catalytic hydrogenation. VI. The reaction of sodium borohydride with nickel salts in ethanol solution. P-2 nickel, a highly convenient, new, selective hydrogenation catalyst with great sensitivity to substrate structure,” Journal of Organic Chemistry, vol. 38, no. 12, pp. 2226–2230, 1973.