What controls the pore spacing in porous anodic oxides?

被引:52
|
作者
Van Overmeere, Quentin [1 ]
Blaffart, Frederic [1 ]
Proost, Joris [1 ]
机构
[1] Catholic Univ Louvain, Inst Mech Mat & Civil Engn, B-1348 Louvain, Belgium
关键词
Anodic oxides; Porous alumina; Perturbation analysis; Internal stress; Surface energy; Electrostatics; SURFACE-DIFFUSION; TIO2; NANOTUBES; ALUMINUM; STRESS; GROWTH; FILMS; ELECTROLYTES; ANODIZATION; TRANSITION; MORPHOLOGY;
D O I
10.1016/j.elecom.2010.06.010
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this paper, we use energy-based perturbation criteria to examine whether strain or electrostatic energy acts as a driving force for porosity initiation in anodic oxides. By doing so, we also succeeded to rationalise the dependence of pore spacing on anodising conditions. Our experimental approach consists of measuring in-situ the internal stress in anodic oxide films grown galvanostatically on aluminium in phosphoric acid, and to correlate these data with the measured pore spacing of the obtained porous films. Our results indicate that the possibility of a strain energy-induced surface instability is unlikely, as for this case the constitutive dependence of pore spacing on internal stress was not verified. Instead, the measured pore spacing, electric field and barrier oxide thickness obtained on our anodic alumina films indicate that electrostatic energy is the main driving force for pore initiation, as well as the factor controlling the pore spacing. Corroborative quantitative evidence for this novel electrostatic-based scaling law is provided by data compiled from the literature for a range of other anodic oxide systems, including nanoporous alumina and nanotubular titania films. (C) 2010 Elsevier B.V. All rights reserved.
引用
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页码:1174 / 1176
页数:3
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