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Study on the Synthesis of Carbon Nanotubes using the Catalyst Metal Deposited Carbon Cathode Electrode in a DC Arc Discharge Process

Published online by Cambridge University Press:  01 February 2011

Hyeon Hwan Kim
Affiliation:
[email protected], Seoul National University, Material Science & Engineering, 56-1 San, Shinlim-Dong, Gwanak-Gu, Seoul, N/A, 151-742, Korea, Republic of, 82-2-880-5451(233), 82-2-887-6575
Hyeong Joon Kim
Affiliation:
[email protected], Seoul National University, Scool of Material Science & Engineering, Korea, Republic of
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Abstract

Carbon nanotubes (CNTs) were grown using a dc arc discharge process and relevant process parameters were investigated. Unlike the usual process in which a carbon anode is filled with metal catalyst powder, CNTs were prepared using a carbon cathode on which the metal catalyst had been deposited using an electroplating system. Various transition metals, Ni, Co and Ti, were used as a catalyst. The results show that multi-walled carbon nanotubes (MWNTs) and single-walled carbon nanotubes (SWNTs) can both be synthesized using this technique. And yield and morphology of the prepared CNTs varied depending on the experimental condition and catalyst. While MWNTs were produced in the deposit and soot sample, SWNTs with diameters near 1nm were only detected in the soot collects. When Ni film was used as a catalyst, the yield of SWNTs was higher than in case of using Co or Ti film as a catalyst. From these results, the optimized preparing condition of CNTs and the properties of a good catalyst are discussed.

Type
Research Article
Copyright
Copyright © Materials Research Society 2006

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References

REFERENCES

1. Zhou, O., Shimoda, H., Gao, B., Oh, S. J., Fleming, L., Yue, G, Acc Chem Res. 35 1045 (2002)Google Scholar
2. Heer, W. A., MRS Bull 281–285 (2004)Google Scholar
3. Ren, Z.F., Huang, Z. P., Xu, J. W., Wang, J. H., Bush, P., Siegal, M. P., Science 282 1105 (1998)Google Scholar
4. Chhowalla, M., Teo, K. B. K., Ducati, C., Rupesinghe, N. L., Amaratunga, G. A., Ferrari, A. C.,Roy, D., Robertson, J., Milne, W.I., J. Appl. Phys. 90 5308 (2001)Google Scholar
5. Zhou, W., Ooi, Y. H., Russo, R., Papanek, P., Luzzi, D. E., Fischer, J. E., Bronikowski, M. J., Willis, P. A. and Smalley, R. E., Chem. Phys. Lett. 350 6 (2001)Google Scholar
6. Park, Y. S., Choi, Y. C., Kim, K. S., Chung, D. C., Bae, D. J., An, K. H., Lim, S. C., Zhu, X. Y., Lee, Y. H., Carbon 39 655 (2001)Google Scholar
7. Tang, D., Xie, S., Zhou, W., Liu, Z., Ci, L., Yan, X, Yuan, H., Zhou, Z., Liang, Y., Liu, D. Liu, W., Carbon 40 1609 (2002)Google Scholar
8. Gamaly, E. G., Ebbesen, T. W., Phys. Rev. B 52 2083 (1995)Google Scholar
9. Dubrovsky, R., Bezmelnitsyn, V., Rev. Adv. Mater. Sci. 5 420 (2003)Google Scholar
10. Ding, F., Bolton, K, Rosen, A.. J. Vac. Sci. Tech. A 22 1471 (2004)Google Scholar