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Self-ordering of anodic porous alumina formed in organic acid electrolytes
New self-ordering porous alumina films were fabricated in organic acid electrolytes. Highly ordered cell arrangements of porous alumina films were realized in malonic acid at 120 V and tartaric acid at 195 V having 300 nm and 500 nm pore intervals, respectively. Self-organization was achieved at the...
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Published in: | Electrochimica acta 2005-11, Vol.51 (5), p.827-833 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | New self-ordering porous alumina films were fabricated in organic acid electrolytes. Highly ordered cell arrangements of porous alumina films were realized in malonic acid at 120
V and tartaric acid at 195
V having 300
nm and 500
nm pore intervals, respectively. Self-organization was achieved at the maximum voltage required to induce high-current-density anodization while preventing burning, i.e., an extremely high-current flow concentrated at local points. The cells of the film grown at a high field must be pressed against each other, so that the self-ordering proceeds with the porous layer growth. When the self-ordering of cell arrangement proceeds, the cells became smaller. To improve the regularity of the cell configuration, a low electrolyte temperature and a relatively high electrolyte concentration were effective for maintaining a high-current-density to prevent burning. Surface flatness was an essential factor for self-ordering, however, the surface oxide film produced by electropolishing an aluminum substrate prevented quick pore growth in the organic acids having a low dissociation constant. It is confirmed that electropolishing followed by alkaline treatment was most appropriate as the pre-treatment in preparing flat surfaces. |
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ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2005.05.058 |