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The Role of Adsorbates on the Field Emission Properties of Single-Walled Carbon Nanotubes

Published online by Cambridge University Press:  15 March 2011

R. Collazo
Affiliation:
Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695-7919
M. Liang
Affiliation:
Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695-7919
R. Schlesser
Affiliation:
Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695-7919
Z. Sitar
Affiliation:
Department of Materials Science and Engineering, North Carolina State University, Raleigh, North Carolina 27695-7919
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Abstract

Two field-emission states of single-walled carbon nanotubes were identified according to their respective emission current levels. The state yielding increased emission current was attributed to the presence of adsorbates on the nanotubes as confirmed by electron emission measurements at different background pressures. Application of high electric fields induced large emission currents and a transition between the two states. During this transition, a current drop to 10% of the original value was observed. Under a constant applied electric field, the current took around 1000 s to recover its original level at a background pressure of 10-10 Torr, while it took half that time at 10-6 Torr. For the high current state, field-emitted electrons originated from states located up to 1 eV below the Fermi level, as was determined by field-emission energy distribution measurements. This suggested that adsorbates introduced a resonant state on the surface that enhanced the tunneling probability of electrons. The adsorbed states are removed at high applied electric fields, presumably due to ohmic heating caused by large emission currents. This adsorption/desorption process is completely reversible.

Type
Article
Copyright
Copyright © Materials Research Society 2002

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References

1 Iijima, S., Nature (London) 354, 56 (1991).Google Scholar
2 Gröning, O., Küttel, O. M., Emmenegger, Ch., Gröning, P., and Schlapbach, L., J. Vac. Sci. Technol. B 18, 665 (2000).Google Scholar
3 Dean, K. A., Allmen, P. von, and Chalamala, B. R., J. Vac. Sci. Technol. B 17, 1959 (1999).Google Scholar
4 Dean, K. A. and Chalamala, B. R., Appl. Phys. Lett. 76, 375 (2000).Google Scholar
5 Rinzler, A. G., Liu, J., Dai, H., Nikolaev, P., Huffman, C. B., Rodriguez-Macias, F. J., Boul, P. J., Lu, A. H., Heymann, D., Colbert, D. T., Lee, R. S., Fischer, J. E., Rao, A. M., Eklund, P. C., and Smalley, R. E., Appl. Phys. A: Mater. Sci. Process. 67, 29 (1998).Google Scholar
6 Schlesser, R., McClure, M. T., McCarson, B. L., and Sitar, Z., J. Appl. Phys. 82, 5763 (1997).Google Scholar
7 Yao, Z., Kane, C. L., and Dekker, C., Phys. Rev. Lett. 84, 2941 (2000).Google Scholar
8 Gadzuk, J. W. and Plummer, E. W., Rev. Mod. Phys. 45, 487 (1973).Google Scholar
9 Dean, K. A. and Chalamala, B. R., Appl. Phys. Lett. 75, 3017 (1999).Google Scholar
10 Schlesser, R., Collazo, R., Bower, C., Zhou, O., and Sitar, Z., Diamond Relat. Mater. 9, 1201 (2000).Google Scholar
11 Collazo, R., Schlesser, R., and Sitar, Z., Appl. Phys. Lett. 78, 2058 (2001).Google Scholar