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The dynamics of the chemical vapor deposition (CVD) of single-walled carbon nanotubes (SWNTs) is extracted experimentally using in situ Raman spectroscopy. Nanotubes are grown using a thin film cobalt catalyst and an ethanol precursor in a miniature hot walled reactor with optical access. Raman spectra at room temperature and at the growth temperature are compared for two growth temperatures. The evolution of the G-band, D-band, and radial breathing mode (RBM) is tracked at the growth temperature with time resolution of a few seconds. There are three identifiable phases in the evolution of the Raman signal intensity: an initial exponential increasing phase, a linear growth phase, and a saturation phase. In situ optical spectroscopy thus enables the study of nucleation, steady growth, and deactivation processes to be investigated separately in real time. The evolution curves for all bands (G, D, and RBM), when scaled, collapse onto the same curve, to within experimental uncertainty.


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The Dynamics of the Nucleation, Growth and Termination of Single-Walled Carbon Nanotubes from in situ Raman Spectroscopy During Chemical Vapor Deposition

Show Author's information Paul Finnie1,2( )Andrew Li-Pook-Than1,2Jacques Lefebvre1
Institute for Microstructural SciencesNational Research Council Canada, Building M-501200 Montreal Road, Ottawa, ONK1A 0R6Canada
Department of PhysicsUniversity of Ottawa150 Louis Pasteur, Ottawa, ONK1N 6N5Canada

Abstract

The dynamics of the chemical vapor deposition (CVD) of single-walled carbon nanotubes (SWNTs) is extracted experimentally using in situ Raman spectroscopy. Nanotubes are grown using a thin film cobalt catalyst and an ethanol precursor in a miniature hot walled reactor with optical access. Raman spectra at room temperature and at the growth temperature are compared for two growth temperatures. The evolution of the G-band, D-band, and radial breathing mode (RBM) is tracked at the growth temperature with time resolution of a few seconds. There are three identifiable phases in the evolution of the Raman signal intensity: an initial exponential increasing phase, a linear growth phase, and a saturation phase. In situ optical spectroscopy thus enables the study of nucleation, steady growth, and deactivation processes to be investigated separately in real time. The evolution curves for all bands (G, D, and RBM), when scaled, collapse onto the same curve, to within experimental uncertainty.

Keywords: chemical vapor deposition, Raman spectroscopy, nucleation, Single-walled carbon nanotube, termination

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Publication history

Received: 19 April 2009
Revised: 19 June 2009
Accepted: 11 August 2009
Published: 22 October 2009
Issue date: October 2009

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© Tsinghua University Press and Springer-Verlag. This article is published with open access at Springerlink.com 2009

Acknowledgements

Acknowledgements

A discovery grant (PF, AL) from Natural Sciences and Engineering Research Council of Canada (NSERC) and a grant (AL) from Le Fonds québécois de la recherche sur la nature et les technologies(FQRNT) are gratefully acknowledged. We are grateful for the ongoing assistance of P. Marshall, Hue Tran, Jeff Fraser and other IMS staff and for preliminary research in this area by Jeffery Bond and Kate Kaminska. We are grateful for the funding of in situ Raman studies via the former JST-CREST "Nanofactory" project led by Yoshikazu Homma.

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