Log Number: P72
Abstract Submitted to the    NANOTUBE'04 Conference:

Nanoauger spectroscopy study of thin film metal catalyst transformation for the production of multi-wall and single-wall carbon nanotubes by chemical method deposition

R. G. Lacerda1, K. B. K. Teo1, F. Wyczisk2, P. Legagneux2, A. S. The1, M. H. Yang1, S. H. Dalal1, D. A. Jefferson1, N. L. Rupesinghe1, D. Roy1, M. Chhowalla3, G. A. J. Amaratunga1 and W. I. Milne1

1 Engineering Department, University of Cambridge, Trumpington Street, Cambridge, CB2 1PZ, UK,
2 Thales Research and Technology France, Domaine de Corbeville, 91404 Orsay, France,
3 Rutgers University, Ceramic and Materials Engineering, Piscataway, New Jersey 08854
Contact e-mail: rgl26@eng.cam.ac.uk

The aim of this work is to study in detail the growth process of multi-wall and single-wall carbon nanotubes from thin metal catalyst by using Nanoauger spectroscopy. The growth is performed by CVD using a thin film triple metal (Al/Fe/Mo) catalyst, by a rapid growth process (gas C2H2, 1000 oC, 5 s) directly on silicon substrates [1]. Recently, a considerable amount of work has been performed using thin film metal layers as the catalyst for nanotube growth, however, the physical phenomena of transforming a thin metal layer into nanosize particles has not been fully understood. We intend to show how the catalyst is transformed and how it diffuses at different growth temperatures. A surface elemental map study is also presented providing a clear view of the distribution of the catalyst on the surface. We observe that during the formation of SWCNT’s at high temperatures (~ 1000 oC), the initial Fe layer (~ 1 nm) is transformed into nano-size particles at the surface. In addition, the Al layer also plays a critical role as a suitable under-layer by being altered into Al2O3 particles. Finally, we will show how Nanoauger spectroscopy can also be used to directly observe single-wall carbon nanotubes.

[1] R. G. Lacerda et al., Appl. Phys. Lett. 84, 269 (2004).

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