Influence of crystal orientation and surface topography of aluminum substrate on pore nucleation of anodic porous alumina

被引:7
作者
Kogakuin University [1 ]
不详 [2 ]
不详 [3 ]
不详 [4 ]
机构
[1] Department of Applied Chemistry, Faculty of Engineering, Kogakuin University, Hachioji, Tokyo 192-0015
来源
Keikinzoku J Jpn Inst Light Met | 2008年 / 8卷 / 375-380期
关键词
Anodic porous alumina; Anodization; Atomic force microscopy; Crystal orientation; Pore initiation;
D O I
10.2464/jilm.58.375
中图分类号
学科分类号
摘要
Pore nucleation and growth processes of anodic oxide films formed on aluminum substrate were investigated by atomic force microscopy with focusing on the crystal orientation and surface topography of aluminum substrate. Nanotopographies of electropolished aluminum were extremely affected by the crystal orientation of aluminum substrate. For as-received aluminum, regularly aligned striped structure appeared after electropolishing. On the other hand, aluminum substrate annealed at 300°C exhibited isotropic hexagonal cell structure. From X-ray diffraction patterns, it was confirmed that the preferential crystal orientation of aluminum was changed from (110) to (100) when annealing temperature was higher than 300°C. In the initial stage of anodization, specific nanotopography of electropolished aluminum surface was served as the initiation sites for pore generation, and accordingly it influenced cell arrangement. Using planarized aluminum with less than 0.3 nm asperities, however, a large number of fine pores initiated on the oxide film surface. Thus, the growth of anodic oxide films was seriously influenced by the surface topography of aluminum substrate.
引用
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页码:375 / 380
页数:5
相关论文
共 11 条
[1]  
Masuda H., Fukuda K., Science, 268, pp. 1456-1468, (1995)
[2]  
Asoh H., Matsuo M., Yoshihama M., Ono S., Appl. Phys. Lett, 83, pp. 4408-4410, (2003)
[3]  
Ono S., Saito M., Ishiguro M., Asoh H., J. Electrochem. Soc, 151, (2004)
[4]  
Oide A., Asoh H., Ono S., Electrochem. Solid-State Lett, 8, (2005)
[5]  
Ono S., Saito M., Asoh H., Electrochimica Acta, 51, pp. 827-833, (2005)
[6]  
Hoar T.P., Yahalom J., J. Electrochem. Soc, 110, pp. 614-621, (1963)
[7]  
O'Sullivan J.P., Wood G.C., Proc. R. Soc. London, A317, pp. 511-543, (1970)
[8]  
Thompson G.E., Furneaux R.C., Wood G.C., Richardson J.A., Goode J.S., Nature, 272, pp. 433-435, (1978)
[9]  
Shimizu K., Kobayashi K., Thompson G.E., Wood G.C., Philosophocal Magazine A, 66, pp. 643-652, (1992)
[10]  
Wu H., Zhang X., Hebert K.R., J. Electrochem. Soc, 147, pp. 2126-2132, (2000)