Hostname: page-component-7479d7b7d-t6hkb Total loading time: 0 Render date: 2024-07-12T13:40:05.502Z Has data issue: false hasContentIssue false

Solubility of carbon nanotubes

Published online by Cambridge University Press:  15 March 2011

Marc In Het Panhuis
Affiliation:
Materials Ireland Polymer Research Centre, Department of Physics, Trinity College Dublin, Dublin 2, Ireland
Jonathan N. Coleman
Affiliation:
Materials Ireland Polymer Research Centre, Department of Physics, Trinity College Dublin, Dublin 2, Ireland
Werner J. Blau
Affiliation:
Materials Ireland Polymer Research Centre, Department of Physics, Trinity College Dublin, Dublin 2, Ireland
Get access

Abstract

We have described a novel experimental technique to separate nanotubes from other unwanted carbon species in arc generated carbon soot. A conjugated polymer was used to bind to nanotubes in solution. The resultant hybrid was soluble while extraneous carbon material formed a sediment at the bottom of the sample bottle. This process was monitored using electron paramagnetic resonance (EPR) which showed that 63% of nanotubes were kept in solution while 98.1% of impurities were rejected. Optimal polymer characteristics for nanotube solubility were identified using geometry optimisation and experimental evidence. It was calculated that a successful polymer has a flat shaped helical backbone with solvent solubilising groups projected outwards. This is achieved with the following polymer characteristics, two solvent solubilising groups on a twist allowing π-conjugated backbone.

Type
Research Article
Copyright
Copyright © Materials Research Society 2001

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

[1] Krätschmer, W., Lamb, L.D., Fostiropoulos, K., Huffman, D.R., Nature (London) 347, 354 (1990).Google Scholar
[2] Bandow, S., J. Appl. Phys. 80, 1020 (1996).Google Scholar
[3] Coleman, J.N., Dalton, A.B., Curran, S., Rubio, A., Davey, A.P., Drury, A., McCarthy, B., Lahr, B., Ajayan, P.M., Roth, S., Barklie, R.C., Blau, W.J., Adv. Mater. 12, 213 (2000).Google Scholar
[4] Holzer, W., Penzkofer, A., Gong, S. H., Bleyer, A., Bradley, D. D. C., Adv. Mat. 8, 974 (1996)Google Scholar
[5] Chauvet, O., Forro, L., Bacsa, W., Ugarte, D., Doudin, B., Heer, W. A. de, Phys. Rev. B. 52 R6963 (1995)Google Scholar
[6] Araki, H., Matsuoka, R., Yoshino, K., Fukuda, M., Mizogami, S., J. Appl. Phys. 69, 7244 (1991)Google Scholar
[7] Ampac 6.0, 1997, Semichem, 7128 Summit, Shawnee, KS 66216, U.S.A.Google Scholar
[8] Bockisch, F., Liotard, D., Rayez, J.C., Duguay, B., Int. J. Quant. Chem. 44, 619 (1992).Google Scholar
[9] M.J.S. Dewar, Zoebisch, E.G., Healy, E.F., Stewart, J.J.P., J. Am. Chem. Soc. 107 3902 (1985).Google Scholar
[10] McCarthy, B., Coleman, J.N., Czerw, R., Dalton, A.B., Panhuis, M. in het, Byrne, H.J., Carroll, D.L. and Blau, W.J., submitted.Google Scholar