Formation mechanism of nanopores in dense films of anodic alumina

被引:1
|
作者
Li, Peng-ze [1 ]
Zhang, Yu [1 ]
Zhang, Jia-zheng [2 ]
Liu, Lin [2 ]
Wang, Shi-yi [1 ]
Liu, Rui [1 ]
Song, Ye [1 ]
Zhu, Xu-fei [1 ]
机构
[1] NanJing Univ Sci & Technol, Key Lab Soft Chem & Funct Mat, Educ Minist, Nanjing 210094, Peoples R China
[2] Jiangsu Ocean Univ, Sch Environm & Chem Engn, Lianyungang 222005, Peoples R China
基金
中国国家自然科学基金;
关键词
anodic alumina; formation mechanism; nanopores; formation efficiency; electronic current; oxygen bubble; GROWTH; BREAKDOWN; OXIDE; TRACER; STRESS; ACID; FLOW;
D O I
10.1016/S1003-6326(24)66585-4
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
Constant-current anodization of pure aluminum was carried out in non-corrosive capacitor working electrolytes to study the formation mechanism of nanopores in the anodic oxide films. Through comparative experiments, nanopores are found in the anodic films formed in the electrolytes after high-temperature storage (HTS) at 130 degrees C for 240 h. A comparison of the voltage-time curves suggests that the formation of nanopores results from the decrease in formation efficiency of anodic oxide films rather than the corrosion of the electrolytes. FT-IR and UV spectra analysis shows that carboxylate and ethylene glycol in electrolytes can easily react by esterification at high temperatures. Combining the electronic current theory and oxygen bubble mold effect, the change in electrolyte composition could increase the electronic current in the anodizing process. The electronic current decreases the formation efficiency of anodic oxide films, and oxygen bubbles accompanying electronic current lead to the formation of nanopores in the dense films. The continuous electronic current and oxygen bubbles are the prerequisites for the formation of porous anodic oxides rather than the traditional field-assisted dissolution model.
引用
收藏
页码:2918 / 2927
页数:10
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