Hostname: page-component-84b7d79bbc-c654p Total loading time: 0 Render date: 2024-07-29T18:23:39.075Z Has data issue: false hasContentIssue false

The synthesis of alumina nanowires on the surface of a porous alumina membrane

Published online by Cambridge University Press:  15 February 2011

R.S. McGrath
Affiliation:
Materials Science and Engineering, University of Nevada Reno, NV 89557-0136, U.S.A.
M. Misra
Affiliation:
Materials Science and Engineering, University of Nevada Reno, NV 89557-0136, U.S.A.
G.P. Sklar
Affiliation:
Materials Science and Engineering, University of Nevada Reno, NV 89557-0136, U.S.A.
J.C. LaCombe
Affiliation:
Materials Science and Engineering, University of Nevada Reno, NV 89557-0136, U.S.A.
Get access

Abstract

Porous aluminum oxide membranes with a complete and even covering of alumina nanowires were formed in a one-step anodization process in dilute phosphoric acid electrolyte. The anodizing conditions can be adjusted to start forming alumina wires that originate on the surface of the porous alumina layer at the triple junction points (the edges of the hexagonal inter-pore structure where three pores meet). The wires tangle together as they become longer; eventually creating a tangled mesh layer above the porous oxide layer. SEM micrographs of the oxide cross section show tapered wires that are approximately 2 to 10 m long, depending on anodizing time, and range in width from a few nanometers to 50nm. The aluminum substrate can be chemically removed and the alumina barrier layer dissolved to leave a free standing porous alumina membrane with very high surface area alumina wires on one face. Some possible future applications of this high surface area structure involve filtration of liquids and gasses, combined with chemical functionalization on the large surface area.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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] Rigby, W.R. et al. , Trans. Inst. Metal Finish. 1990, 68 (3), 95.Google Scholar
[2] Li, A. P. et al. , J. of App. Physics, 84 (11), 1998.Google Scholar
[3] O'Sullivan, J.P. and Wood, G.C., Proc. Roy. Soc. Lond. A. 1970, 317, p511543.Google Scholar
[4] Xiao, Z. L., et all. Nano Letters. 2002, 2 (11), p12931297.Google Scholar
[5] Tian, Y.T., et all. Nanotechnology. 2004, 15, p189191.Google Scholar
[6] Xu, T.T., et all. Langmuir. 2003, 19, p14431445.Google Scholar
[7] Yuan, J.H., et all. Chem. Mater. 2004, 16, p18411844.Google Scholar
[8] Jessensky, O., et all. App. Phys. Letters. 1998, 72, 10.Google Scholar
[9] Ono, S., et all. J. of the electro. Chem. Society. 2004, 151, 8.Google Scholar
[10] Li, F, et all. Chem. Mater. 1998, 10, p24702480.Google Scholar
[11] Thompson, G.E.. Thin Solid Films. 1997, 297, 192210.Google Scholar
[12] Sui, Y.C., Thin Solid Films. 2002, 406, 6469.Google Scholar
[13] Itoh, N., J. of Membrane Sci. 1996, 117, 189196.Google Scholar
[14] Stirland, D.J. and Bicknell, R.W., J. Electrochem. Soc. 1959, 106, 481.Google Scholar
[15] Altenpohl, D., Conv. Record of I.R.E. 1954, 3, 35.Google Scholar
[16] Diggle, J.W., et all. Chem. Reviews. 1969, 69, 3, 365405.Google Scholar